Iodine-125 brachytherapy for brain tumours - a review
© Schwarz et al; licensee BioMed Central Ltd. 2012
Received: 5 January 2012
Accepted: 6 March 2012
Published: 6 March 2012
Iodine-125 brachytherapy has been applied to brain tumours since 1979. Even though the physical and biological characteristics make these implants particularly attractive for minimal invasive treatment, the place for stereotactic brachytherapy is still poorly defined.
An extensive review of the literature has been performed, especially concerning indications, results and complications. Iodine-125 seeds have been implanted in astrocytomas I-III, glioblastomas, metastases and several other tumour entities. Outcome data given in the literature are summarized. Complications are rare in carefully selected patients.
All in all, for highly selected patients with newly diagnosed or recurrent primary or metastatic tumours, this method provides encouraging survival rates with relatively low complication rates and a good quality of life.
The implantation of radioactive material into tumours was proposed by Pierre Curie in 1901 . In 1951, Friedlander and Orr prepared iodine-125 by alpha bombardment of natural antimony . In 1965, this nuclide was finally introduced in interstitial cancer therapy (prostate, lung cancer and lymph nodes) . Mundinger played a pioneering role in the development of the concept of brachytherapy in brain tumours: he began to implant iridium-192 wires into gliomas at 1960; since 1979 he has preferred iodine-125 seeds [4, 5]. Nowadays, temporary implantation of iodine-125 seeds is preferred for interstitial brachytherapy in brain tumours. Despite favourable physical and biological characteristics of brachytherapy and well established implantation techniques, so far brachytherapy treatment of brain tumours has been performed in only a few centres worldwide. The current review considers radiobiological characteristics, indications, and treatment effects of iodine-125 brachytherapy (including side effects) for patients with brain tumours.
Rationale for stereotactic iodine-125 brachytherapy
Interstitial brachytherapy aims for a highly localized devitalisation of a well defined treatment volume, thereby avoiding damage of the surrounding non-neoplastic tissue. Treatment volume and target volume are ideally identical. The minimal-invasive, spatially precise stereotactic implantation technique, in combination with favourable physical characteristics of the radioactive sources, enable the accurate application of highly focused necrotizing tissue dose with a steep fall-off from the centre to the periphery. The pronounced dose inhomogeneity within the target volumes make iodine-125 brachytherapy an attractive concept, particularly for selected patients suffering from small, circumscribed tumours at any location of the brain. Of note, stereotactic brachytherapy must not be confused with stereotactic radiotherapy, which exhibits much less dose inhomogeneity and lower intratumoural (non-necrotizing) doses, and stereotactic radiosurgery, which is characterized by the absence of any effects of fractionation [6–10].
Physical characteristics, dosage and dosimetry
Conventional fractionated irradiation is administered with a dose rate of about 200cGy/min. In contrast, interstitial irradiation aims for much lower dose rates of < 100cGy/h. This continuous low-dose rate irradiation increases the therapeutic ratio as the ongoing repair of sublethal irradiation doses is more effective in non-neoplastic tissue, than in tumour (see below).
Isotopes used for brachytherapy in brain tumours (Adapted from ).
Mean energy (MeV)
To calculate the total dose for permanent iodine-125 implants the mean life time of 87 days is used . As compared with alternative permanent implants (Au-198 and Pd-103), I-125 has been shown to be more effective on slow growing tumours (tumour doubling time of > 10 days) .
Principles of seed positioning aim for a good coverage of the target volumes with an acceptable uniformity of the dose distribution by a minimal number of catheter implants while sparing the surrounding anatomical structures (i.e. normal brain tissue, vessels, optic nerve etc.) from radiation exposure [28–33]. Usually, one to five seeds, encapsulated in the tip of a Teflon catheter, are necessary to achieve a conformal interstitial irradiation, even of complexly shaped tumour volumes. Of note, iodine-125 seeds are available in various shapes, making their dose distribution non-isotropic, which must be considered for therapy planning [11, 14, 34–40]. The tri-planar treatment-planning system is based on stereotactic computed tomography (CT) and magnetic resonance imaging (MRI), as well as novel metabolic imaging data. It allows positioning of seeds within target volumes, generate and display the resulting isodose distribution and calculate approach angles [32, 41, 42]. Care has to be taken that the high dose zones (> 150Gy) always lie within the tumour tissue and that vessels are not adjacent to these zones .
The definition of target volumes has changed over time. In the beginning of seed implantation in brain tumours, the target volume was mostly determined to be the tumour visible in CT, plus an isotropic margin of 0.5 cm [23, 30, 44–47]. Presently, image fusion with magnetic resonance imaging and positron emission tomography allows a better visualisation and more precise definition of the target volume . Schupak et al. found out that the technical accuracy had an impact on the local failure rate but not on the overall survival of the patients .
The following parameters should be documented for each stereotactic brachytherapy: prescribed total dose, dose rate, minimum tumour dose, percentage of the tumour receiving less than the prescribed dose, maximum dose in "normal" brain at 1 cm from the tumour border, number of seeds, activity of seeds, volumes of tumour and surrounding tissue irradiated to various total doses and dose rates .
In summary, the accurate dose distribution, the rapid dose decrease from the centre of the treatment volume towards the periphery, and the high doses in the tumour and the low doses in the normal tissue, are great physical advantages of iodine-125 implants for brain tumour therapy .
Theoretical models and cell culture experiments
Dale et al. have adapted the linear-quadratic (LQ) model for protracted radiotherapy, incorporated tumour repopulation and tumour shrinkage factors, to allow radiobiological assessment of permanently implanted iodine-125 seeds [50–52]. Using the conventional linear-quadratic model with an α/β = 10Gy for tumour tissue and an α/β = 3Gy for healthy tissue and given a repopulation resulting in a loss of 0.4Gy/d, 60Gy of temporary implants in 5 days are almost equivalent to 100Gy permanent implant dose .
Even though the conventional LQ model describes well the radiobiological effects of an implant at the boundary of the target volume, it does not account for the effects of extreme dose inhomogeneity associated with brachytherapy . Characteristic tissue effects associated with the high dose zone in the vicinity of the implanted source (≥ 200Gy) have been described experimentally, i. e. the development of circumscribed radionecrosis with temporary changes in capillary permeability with a sometimes extensive oedema and concomitantly reduced regional cerebral blood flow [18–20, 55, 56] (see below).
The overall low-dose-rate of iodine-125 allows reoxygenation for increasing radiosensitivity and cancels out the repair of sublethal damage. Normal tissue irradiation is essentially reduced because the exposure level decreases by the inverse square of the distance from the source. Therefore, the rate of tumour cell killing of brachytherapy has been thought to be much greater than that of conventionally fractionated teletherapy .
Animal experiments and histological studies
Iodine-125 brachytherapy reduces histological features that are prognostic for tumour progression, i.e. cellularity, pleomorphism, vessel hyperplasia and degree of mitosis, and lowers the proliferating cell nuclear antigen, a marker for late G1- and S-phases of the cell cycle .
To examine how the tumour microenvironment (perfusion, oxygen partial pressure) changes in response to low-dose-rate brachytherapy, experiments with a mouse hypoxic tumour model have been performed. The perfusion is elevated at a distance of 2-4 mm from the seed, starting three days after implantation, and pO2 is increased one to three days after implantation. Therefore, additional external beam radiotherapy should be most advantageous 1-2 days after implantation, when pO2 is high, and chemotherapy most advantageous 3-4 days after implantation, when perfusion is high .
Autopsy material showed that the early phase after implantation is characterized by migrating macrophages and removal of necrotic debris. In the established phase, a necrotic centre and a reactive zone around have been found. The reactive zone consists of a narrow inner rim of microglial accumulation and a broader outer area with astrocytic gliosis, vascular proliferation, activated microglia and infiltration by macrophages. In the burned-out phase the necrosis undergoes liquefaction, the microglia rim is replaced by end-stage macrophages and the reactive zone is transformed into astrocytic gliosis equivalent to a scar [55, 63].
A radiomorphological triple ring formation has been identified to be characteristic after seed implantation (see below) and correlates with histopathological alterations including a coagulative necrosis in the central radiolucent region, a fibrinoid necrosis of vessel walls within the ring enhancement and an adjacent spongiosis and gliosis, as well as oedema . With increasing time after implantation the ring enhancement moves outward .
The effect of permanent iodine-125 implants on the blood-brain barrier (BBB) function was additionally studied in normal canine brains. The breakdown of the BBB occurs as soon as 7 days after implantation. The radiation lesion enlarges rapidly from day 7 to 72, then increases more slowly until day 392 and is relatively decreased in size in 2 years. Furthermore, the finding of the three zones with calcified necrosis, a narrow fluid-filled zone and a narrow rim of viable but damaged tissue in which there is breakdown of the BBB for up to 1 year before returning to an almost normal function at 2 years, were confirmed. Increased permeability was most pronounced in white matter as compared to grey matter .
Summary of biological characteristics
Due to the continuous low-dose rate irradiation, especially in the periphery of the target volume and at the edge to normal tissue, sublethal damage can be repaired and long term side effects of the late-responding tissue can be avoided. In the centre of the treated volume, highly focused necrotizing intratumoural doses with a steep dose decrease from the centre to the periphery, such as in radiosurgery, can be achieved. Therefore, seeds combine the advantages of fractionated radiotherapy (repair of surrounding normal tissue) and radiosurgery (tumour cell death irrespective of radiosensitivity) in one modality.
Because repopulation and redistribution during the treatment are of minor importance in the therapy of low grade gliomas, low dose rate seed implantation appears to be a rational therapeutic strategy .
Stereotactic biopsy and implantation techniques
Obtaining tissue diagnosis and molecular genetic profiling are mandatory for each suspected brain tumour. This can be routinely performed by means of stereotactic biopsy procedures that integrate CT, MRI and metabolic imaging data for trajectory planning and enable minimal-invasive collection of representative specimens throughout entire tumour volumes (including biologically "hot spots" if present), especially for those tumours that are not eligible for gross open tumour resections [16, 65, 66]. Therefore, the authors promote a stage concept of interstitial brachytherapy after versatile tissue diagnosis and molecular genetic profiling of the brain tumours have been obtained.
Indications for iodine-125 brachytherapy
Iodine-125 brachytherapy is a valuable treatment option for patients with non-resectable, small, and circumscribed untreated tumours in any location of the brain, as well as local circumscribed recurrences after previously performed percutaneous radiotherapy and/or surgery . Ideally, the diameter of the tumour should be smaller than 3 cm. In case of larger tumour volumes, microsurgery (partial resection) might be combined with brachytherapy . Of note, interstitial brachytherapy can be performed even in cases in which tolerance of the healthy brain tissue has been reached because of previous external irradiation and/or stereotactic radiosurgery [4, 76]. Implantation is also a valuable technique in certain paediatric patients [77, 78]. For a long time, infratentorial masses, the hypothalamic region, the middle-inferior mesencephalon, the diencephalon, the pons, the corpus callosum and tumours with subependymal or transcallosal spread, involvement of the cerebellum, the brainstem or the deep thalamic regions, involvement of basal ganglia structures, sylvian or interhemispheric fissures, have been considered contraindicated sites for implantation. Furthermore, large tumours > 6 cm or with a tumour volume of > 120 ml, multifocal masses, and those with diffuse margins, patients with a Karnofsky performance status (KPS) of < 60 and significant oedema, have been thought to be not suitable for implantation [12, 13, 46, 73, 79–82]. Currently, technical indications have been extended [83, 84]. Only diffuse tumours, tumours with a diameter larger than 4 cm, or with infiltration of the corpus callosum, are still considered to be insuitable for implantation .
During MRI follow-up evaluation, a characteristic triple ring formation can be identified, which should not be confused with tumour progression . The inner zone of this formation refers to the necrotized tumour, the intermediate contrast enhanced zone to a small rim of a still viable tumour, exhibiting increased capillary permeability, and the outer zone to the treatment induced oedema. The ring shaped area of contrast-enhancement is visible 4.5 months to 3 years after implantation . A study on volumetric changes in tumour necrosis, reactive zone and oedema over the time after temporary seed implantation (50-60Gy) has revealed the following: compared to the reference dose volume the necrosis has been 19.9% after 6 months, 8.3% after 14 months and 7.0% after 24 months, the reactive zone 30.4%, 34.8% and 16.7%, respectively, and the oedema 293.2%, 220.5% and 107.0%, respectively. Necrosis has been found in regions with > 79.2Gy with a maximum 6 months after irradiation, a shrinkage between 9 and 15 months and a steady-state after 16 months. The reactive zone has had its maximum 2 months after irradiation, after 12 months the shrinkage has been more pronounced. The maximum of the oedema has been reached after 6 months .
Other visible late radiation effects (> 2 months) are decreased enhancement of the tumour region, decreased mass effect, atrophic changes in surrounding brain (widened sulci), calcification in areas immediately adjacent to the seeds, and focal necrosis corresponding to the treatment volume, surrounded by a zone of decreased cerebral metabolism in positron emission tomography (PET) .
To monitor iodine-125 brachytherapy effects in low-grade gliomas with PET L-methyl-carbon-11-methionine uptake seems to be more suitable than 2-fluoro-18-1-deoxy-D-glucose (FDG), as it shows a dose dependent decline in uptake [87, 88].
A magnetic resonance imaging study compared longitudinally features of patients either treated with external beam radiotherapy alone or in combination with brachytherapy. In both groups, nodular enhancement adjacent to or remote from the resection cavity strongly suggests tumour recurrence. Linear rim enhancement, later on progressing to feathery enhancement, immediately adjacent to the cavity, has been seen in brachytherapy patients only and strongly indicates radiation necrosis .
Clinical indications and results
Results concerning survival achieved with permanent and temporary iodine-125 brachytherapy in patients with various brain tumours.
Number of patients &
type of iodine-125 seeds
Dose, dose rate, activity
Diagnoses (number of patients) & additional percutaneous radiotherapy (pRT)
6 months-survival rate
9 months-survival rate
12 months-survival rate
18 months-survival rate
2 year-survival rate
3 year-survival rate
4 year-survival rate
5 year-survival rate
8 year-survival rate
10 year-survival rate
15 year-survival rate
221 iodine-125 & iridium-192
Astrocytomas I (55)
Astrocytomas II (76)
Astrocytomas III (34)
Oligodendrogliomas II/III (26)
Recurrent primary tumours
> 18 months
Recurrent malignant gliomas
Recurrent primary tumours
Astrocytomas III (42)
Astrocytomas III (23)
New tumours (12)
Additional pRT (45Gy)
Recurrent tumours (4)
New glioblastomas (5)
Additional pRT (50.4Gy)
Recurrent tumours (12)
Astrocytomas III (8)
Astrocytomas III (50)
56 temporary & permanent
Astrocytomas I (36)
Astrocytomas II (14)
Astrocytomas III (6)
Astrocytomas III (2)
Recurrent tumours (10):
11 months (mean)
Astrocytomas III (3)
Additional pRT (50-60Gy)
Astrocytomas III (5)
8 months (mean)
Astrocytomas III (50)
Astrocytomas III (20)
Additional pRT (60Gy)
Astrocytomas III (50)
Astrocytomas III (23)
Additional pRT (50Gy)
Astrocytomas III (18)
Radiation-induced tumours (2)
Additional pRT (59.4Gy)
Astrocytomas III (25)
Additional pRT (60Gy)
Astrocytomas III (29)
Additional pRT (60Gy)
Astrocytomas III (4)
Recurrent Glioblastomas (25)
Astrocytomas III (80)
Astrocytomas III (70)
Additional pRT (50Gy)
permanent only (9)
Zamorano 1992 
11 months (mean)
Astrocytomas III (3)
Additional pRT (50-60Gy)
Astrocytomas III (5)
8 months (mean)
Astrocytomas III (29)
Additional pRT (60Gy)
Astrocytomas III (50)
Astrocytomas III (16)
Astrocytomas III (7)
Astrocytomas III (8)
Astrocytomas III (36)
Astrocytomas III (7)
Additional pRT (60Gy)
Astrocytomas III (32)
Additional pRT (40-77Gy)
194 temporary 345 permanent
Astrocytomas I (106)
Astrocytomas II (251)
Astrocytomas III (75)
WBRT (40Gy) + seed (38)
Seed only (22)
WBRT (40Gy) only (49)
seed only (21)
Astrocytomas III (9)
Additional pRT (66Gy@2x1.1Gy/d)
Astrocytomas II (251)
Oligoastrocytomas II (44)
Oligodendrogliomas II (29)
Additional pRT (56-60Gy)
Additional pRT (59.4Gy @1.8Gy/d or 40Gy@2x2Gy/d)
Astrocytomas II (2)
Astrocytomas III (12)
60Gy or 80-300Gy
Astrocytomas III (9)
Astrocytomas III or Glioblastomas (26)
Astrocytomas III or Glioblastomas (73)
> 31 months
Additional pRT (50-60Gy)
(16% before, 68% concurrent, 15% not)
> 23 months
Recurrent astrocytomas III or glioblastomas (23)
Astrocytomas III (45)
Additional pRT (50-60Gy)
(62% before, 24% after, 14% not)
43Gy or 90Gy
Astrocytomas I (2)
14 temporary 22 permanent
32cGy/h or 42cGy/h
Astrocytomas II (23)
Additional pRT (30-54Gy)
Astrocytomas III (45)
Additional pRT (50-60Gy)
(24% before, 63% after, 14% not)
Astrocytomas III (3)
Oligodendrogliomas III (1)
194 temporary 261 permanent
Astrocytomas I (97)
Astrocytomas II (250)
Gemistocytic gliomas (21)
Astrocytomas III (40)
> 31 months
> 23 months
Additional pRT (50-60Gy)
(17% before, 66% after, 17% not)
Additional pRT (40-77Gy)
Seed + pRT (40Gy) (38)
seed only (34)
Astrocytomas III (4)
197 temporary & permanent
Astrocytomas II (153)
Oligoastrocytomas II (44)
Additional pRT (47)
New high-grade gliomas
Recurrent high-grade gliomas
Additional pRT (30-75Gy)
Recurrent glioblastomas (15)
Malignant astrocytomas (140)
Additional pRT (50Gy) (63)
only pRT (50Gy) (69)
Astrocytomas III (22)
Astrocytomas III (22)
Additional pRT (50-60Gy)
Recurrent glioblastomas (38)
Recurrent glioblastomas (40)
Additional pRT (10-30Gy)
Recurrent paediatric tumours:
Primitive neuroectodermal tumours (2)
preirradiated (3 craniospinal, 2 WBRT)
Additional pRT (57-61Gy)
Astrocytomas III (57)
Oligodendrogliomas III (3)
Additional pRT (50-60Gy)
(78% before, 22% not)
Recurrent glioblastomas (35)
55 temporary & permanent
Astrocytomas II (46)
Oligoastrocytomas II (9)
Astrocytomas II (187)
Oligoastrocytomas II (52)
Paediatric astrocytomas I (12)
Astrocytomas I/II (27)
Astrocytomas III (10)
New tumours (11)
Recurrent tumours (32)
Additional pRT (60Gy@ 2x1Gy/d)
New astrocytomas II (18)
Recurrent astrocytomas II (13)
Recurrent glioblastomas (34)
New metastases (19)
Recurrent metastases (21)
Astrocytomas I (4)
Astrocytomas II (30)
Astrocytomas III (11)
Pinealis tumour (1)
Ruge 2011 
Korinthenberg 2011 
Astrocytomas I (53)
Astrocytomas II (26)
Oligoastrocytomas II (4)
Oligodendrogliomas II (5)
Ependymoma II (1)
Not classified (5)
El Majdoub 2011 
Recurrent Medulloblastomas (12)
Ruge 2011 
Suchorska 2011 
Astrocytomas II (69)
Oligoastrocytomas II (14)
Oligodendrogliomas II (12)
Ruge 2011 
Astrocytomas I (101)
Astrocytomas II (34)
Ruge 2011 
Brachytherapy of pilocytic astrocytomas WHO grade I
Pilocytic astrocytomas frequently involve paediatric patients. Open tumour resection remains to be the gold standard, with favourable survival rates, provided complete tumour removal has been achieved. Unfortunately, these tumours are often found in highly eloquent locations such as the chiasmatic/hypothalamic area, the thalamus, the tractus opticus etc., rendering a complete resection impossible for a considerable number of patients. Poor physical, cognitive, and psychosocial outcome scores have been reported after long-term follow-up evaluation in particular for those patients with deep-seated tumour locations (diencephalon, optic chiasm, etc.). In here, an unfavourable outcome was at least partly attributed to side effects of surgical treatment [90–92].
In 1980, Mundinger et al. reported the first survival results of 55 young patients with diencephalic pilocytic astrocytomas treated with iodine-125 or iridium-192 interstitial brachytherapy. In this patient population 3- and 5-year survival rates of 72% and 52% have been achieved . In paediatric patients the 1-, 3- and 5-year survival rates were slightly better for permanent iridium-192 (88%, 70% and 55%) than for iodine-125 implants (86%, 58% and 22%). Both nuclides proved to be more effective than biopsy or partial resection only . Others report a 2-year survival rate of 83% for paediatric patients and temporary iodine-125 implants .
Another retrospective analysis revealed 1- and 3-year survival rates of 94% and 73% for newly diagnosed (treated in combination with percutaneous radiotherapy) and of 68% and 30% for recurrent (treated with brachytherapy alone) low grade gliomas .
The largest series with 106 pilocytic astrocytoma patients was published by Ostertag and Kreth. Patients were either treated with permanent or temporary implants; a 5-year survival rate of 77% was obtained and radiation toxicity was mostly observed in patients treated with permanent implants . 5- and 10-year survival rates of up to 85% and 83% have been reported by another publication .
Of note, treatment of a subpopulation of 45 highly eloquent hypothalamic tumours was associated with low risk and provided similar clinical outcome rates. Peraud and co-workers report on clinical outcome after temporary iodine-125 implantation (54Gy, 8cGy/h, < 20mCi) for complex located WHO grade I and II gliomas (including 4 mesencephalic/pontine, 2 thalamic/pineal and 2 mesencephalic/pontine tumour locations) . A complete response after brachytherapy was seen in four patients, and a partial response in seven patients. None of the patients exhibited tumour progression within a median follow-up of 31.5 months, and no radiogenic complications occurred. Of note, functional outcome scores were favourable with significant improvement of pre-existing hemiparesis in 3/4 patients, improvement of endocrine deficits in one half of patients, and improvement of visual functioning in 1/3 patients. Other retrospective data are in line with these findings . Of note, long term side effects of brachytherapy seem to be rare in the paediatric subpopulation .
To summarize, studies on brachytherapy in pilocytic astrocytomas WHO grade I are rare and retrospective. Therefore, no clear conclusion can be drawn concerning indications for brachytherapy for these tumours. However, stereotactic iodine-125 brachytherapy has been shown to be a safe, minimally invasive, and an effective first-line treatment option for selected patients with highly eloquent tumour locations, bearing a high risk for open tumour resection. As pilocytic astrocytomas are mostly slow growing, sharply marginated tumours in the midline and highly eloquent areas, brachytherapy should be considered an attractive option.
Brachytherapy of gliomas WHO grade II-IV
Many more patients with gliomas WHO grade II-IV have been treated with iodine-125 implants. However, the place of interstitial brachytherapy remains poorly defined. Moreover, the effects of an oligodendroglial differentiation, as well as recently discovered molecular genetic markers (such as LOH1p/19q, TP53 mutations, MGMT promoter methylation and IDH1 mutations), on the efficiency of interstitial brachytherapy, have not been evaluated yet .
Brachytherapy of gliomas WHO grade II
Results of brachytherapy for low grade gliomas WHO grade II - as first line treatment option - have been already summarized before . Most data come from retrospective studies: 1-, 3- and 5-year survival rates in the range of 79-94%, 36-73% and 21-65% for primary tumours and 1- and 3-year survival rates of around 68% and 30% for recurrent tumours have been reported [4, 12, 25, 67, 68, 93, 95, 98–101].
The response rates of astrocytomas WHO grade II for iodine-125 brachytherapy included 7.5-25.8% complete responses, 13.8-29.0% partial responses, and 45.2-61.1% stable diseases. The rate of non-responders ranges between 0% and 17.6% [67, 102].
One of the largest long-term analysis (median follow-up: 10.3 years) reports on interstitial brachytherapy in 239 patients with progressive eloquently located circumscribed, supratentorial WHO grade II gliomas . In 103 patients permanent implants were used, since 1985 temporary implants have been preferred. Five-, 10-, and 15- year progression free survival was 45%, 21%, and 14%, respectively. The corresponding survival rates were 51%, 32%, and 22%, respectively. Of note, no levelling off of the Kaplan Meier curves was observed and patients experienced tumour progression even 10 years after treatment. Complete response was seen in 18 patients, partial response in 33 patients, tumour control in 146 patients, and unrestrained tumour progression in 42 patients (non-responder group). Transient radiogenic complications occurred in 19 patients.
Schnell et al. found a 5-year survival rate as high as 93% in patients with low activity temporary iodine-125 implants (54Gy, 10cGy/h) .
Malignant transformation of astrocytomas II was seen in 33% of the patients after 5 years, in 54% after 10 years and in 67% after 15 years , but was not different to open tumour resection alone .
In a retrospective analysis, Warnke and co-workers observed a significant reduction of seizure incidence and increase of benzodiazepine receptor density (as demonstrated by single photon emission computed tomography in a subset of 20 patients), after brachytherapy of 80 patients with temporal WHO grade II astrocytomas . Of note, 79% of patients became seizure free after six months.
For astrocytomas grade II, a significantly better outcome with less radiation toxicity was reached with temporary seeds than with permanent ones, which are associated with an increased risk for prolonged oedema [95, 100, 101, 104]. Target volume and radiation dose showed a direct correlation with the risk of radionecrosis with critical values being 35 cm3 and 100Gy for permanent and 50Gy at 42cGy/h for temporary implants . Age, KPS, midline shift, tumour volume and enhancement on CT were predictors for outcome [68, 95, 99–101].
A combination of microsurgery and stereotactic brachytherapy for tumour remnants is feasible and might be an alternative treatment strategy, for example, for large lesions with significant proportions of eloquent tumour parts to avoid neurological deficits . Brachytherapy to treat progressive or recurrent tumours after resection achieved a tumour response rate of 35.9% and a control rate of 97.3% after 24 months; median progression free survival was 53 months .
All in all, even though stereotactic brachytherapy has been used for low-grade gliomas for many years, its place within the multimodality treatment concept is still debated . Small (less than 4 cm in diameter), circumscribed lesions in highly eloquent or deep-seated tumour locations might be good candidates for interstitial brachytherapy, especially in cases harbouring an increased risk for open tumour resection. Moreover, radiobiology, tumour shape and the option of percutaneous radiotherapy for recurrence, favour an increased application of brachytherapy in astrocytomas grade II.
Brachytherapy of anaplastic gliomas WHO grade III
For newly diagnosed anaplastic astrocytomas WHO grade III, standard therapy consists of radiation therapy with/-out surgical resection, whenever safely possible. Alternatively, first line chemotherapy might be considered (NOA-04 study). However, interstitial brachytherapy might also be a local treatment option, especially for those patients that are not clear surgical cases.
For newly diagnosed anaplastic astrocytomas, the combination of interstitial brachytherapy with percutaneous radiotherapy has been shown to be associated with 1-, 2-, 3- and 5-year survival rates of 33-87%, 36-75%, 17-66% and 0-50%. Median survival is also highly variable and ranges between 8-57 months. Patients treated with seeds for recurrent anaplastic astrocytomas had 1-, 2- and 3-year survival rates of 49-81%, 46-55% and 24-40% and a median survival of 9-35 months after implantation [4, 23, 25, 44, 45, 53, 81, 93, 95, 98, 107–124].
Two studies found an enhanced median survival in patients treated with percutaneous radiotherapy in combination with temporary iodine-125 implants, compared to external irradiation alone [24, 125]. While in the NCOG 6G-82-2 study, the brachytherapy boost had no additional advantage .
Gutin et al. compared survival after iodine-125 brachytherapy for recurrent anaplastic astrocytomas to that of a historical chemotherapy group and obtained better survival data for the brachytherapy group .
Factors associated with improved survival were age ≤ 45-50 years, KPS ≥ 80-90, superficial location, decreasing volume of implanted tumour, chemotherapy at recurrence and reoperation at the original site in case of tumour recurrence [24, 117, 124, 126].
Different schemes have been used for primary therapy. On the one hand, 50-60Gy of temporary implants have been combined with 50-60Gy percutaneous radiotherapy [24, 81, 107]. On the other hand, 100Gy of permanent implants have been added to 50-60Gy external beam radiotherapy . Sometimes seeds had been implanted before percutaneous radiotherapy had been started .
There was as well a lot of variation in therapy for recurrent, pre-irradiated astrocytomas III. Doses of 50-150Gy have been employed with temporary implants [44, 45, 107, 111, 127]; 100-300Gy with permanent [53, 128].
To summarize, multiple, even several randomized, studies were performed to analyze the value of brachytherapy in the primary treatment of astrocytomas grade III, but failed to prove any clear beneficial efficacy for this tumour entity. Therefore, standard therapy is radiotherapy or chemotherapy according to the results of the NOA-04 study . However, for recurrent, pre-irradiated tumours, seeds might be a valuable option.
Brachytherapy of glioblastomas WHO grade IV
Interstitial brachytherapy has been repeatedly suggested for malignant gliomas WHO grade IV at primary diagnosis, as well as during the course of the disease. For primary glioblastomas, 1-, 2-, 3- and 5-year survival rates of 80-91%, 19-57%, 14-40% and 9-18% and a median survival of 13-26 months could be achieved. 1-, 2- and 3-year survival rates for recurrent tumours were 44-66%, 13-26% and 8-15%, and median survival 6-17 months [4, 23, 25, 44, 45, 53, 81, 95, 108–119, 121–123, 128, 130–142].
Several retrospective studies showed a better survival for patients with primary glioblastomas treated with a temporary or permanent brachytherapy boost, in addition to parallel or sequential external beam irradiation, instead of percutaneous radiotherapy alone (e.g. 1-, 2-, 3- and 4-year survival rates have been 40%, 12.5%, 9% and 5% compared to 83-87%, 34-57%, 27% and 16%; median survival 11 months vs. 18 months) [134, 137]. There was no survival difference for iridium-192 and iodine-125 , or brachytherapy and radiosurgery boost , but permanent implants showed improved survival compared to temporary .
Percutaneous and interstitial irradiation in newly diagnosed paediatric malignant gliomas have been complemented by high-dose chemotherapy and autologous bone marrow rescue, but was not associated with better outcome scores than for conventional regimens .
For recurrent glioblastomas, tumour resection plus permanent seed implantation was compared to biopsy plus temporary seed implantation, and revealed similar median survival rates .
Subgroup analyses of the results for primary treatment of anaplastic astrocytomas and glioblastomas with percutaneous radiotherapy and permanent brachytherapy boost, divided into the RTOG recursive partitioning analysis (RPA) classes, have shown the following results: the 2-year survival rate and the median survival for RPA classes I/II were 68% and 37 months, for class III 74% and 28-31 months, for class IV 32-34% and 16 months and for classes V/VI 29% and 11 months. Iodine-125 has improved the survival most demonstrably in poorer prognostic classes so that a selection bias does not account for the survival benefit [121, 122].
Age has an important effect on survival with a median survival of 109 weeks for patients aged 30-40 years, 96 weeks for 40-50 years, 77 weeks for 50-60 years and 76 weeks for 60 years and older . Other factors affecting outcome were KPS, superficial lesion, gross total resection, reoperation, residual tumour volume, number of seeds, seed activity, volume implanted and dose [25, 117, 126, 140, 142, 144].
A recurrence pattern analysis of patients treated in the NCOG 6G-82-2 trial revealed that 77% were local (within 2 cm from seed), 14% separate, 5% subependymal and 5% systemic . Others found 35% local, 65% marginal and 28% distant relapse  or 70% local, 18% distant and 12% both .
Many different dose combinations of percutaneous radiotherapy and iodine-125 brachytherapy have been given in the primary therapy setting; 45Gy whole brain radiotherapy and 100-280Gy (15-30cGy/h) brachytherapy boost , 59.4Gy (1.8Gy, 5×/week) or 40Gy (2Gy, 2×/day) and a high activity brachytherapy boost of 50Gy , but most percutaneous and temporary seed dose were 60Gy [139, 141]. Sometimes radiotherapy was combined with chemotherapy regimens [109, 118, 125, 138] or hyperthermia , or was given after seed implantation .
For pre-irradiated, recurrent glioblastomas, seeds have been implanted only without further percutaneous radiotherapy. 100-500Gy of permanent seed dose have been chosen [140, 142] or 50-120Gy of temporary [44, 110, 111].
All in all, multiple studies for newly diagnosed glioblastomas have been performed, but brachytherapy does not play a role in this setting nowadays. Standard therapy is surgery and radiotherapy, plus concomitant and adjuvant temozolomide . In the recurrent setting, brachytherapy might be an option as interstitial irradiation can still be employed in cases in which tolerance of the healthy brain tissue has been reached because of previous external irradiation . Interstitial irradiation offers excellent palliation in a majority of patients with a significant amount of long-term survivors for recurrent gliomas .
Brachytherapy of brain metastases
Besides primary brain tumours, interstitial brachytherapy should be considered for brain metastases [148, 149]. Some accept a maximum diameter of 4 cm , others implant 3-6 cm metastases that are beyond the size limit of radiosurgery . The advantages of treating brain metastases with brachytherapy are a minimally invasive procedure, a minimal damage to normal brain tissue, no supplementary risk by anaesthesia, no interference with other therapeutic modalities, low stress for the patient, a short hospitalisation time (2-3 days) and low costs. The reasons why brain metastases are ideal for interstitial irradiation are the frequent spherical shape, the mostly relatively small size, the normal brain parenchyma being displaced outside the potential target volume and the minimally invasive growth .
Kreth et al. compared the median survival after iodine-125 brachytherapy (60Gy, 10cGy/h, temporary), percutaneous radiotherapy (40Gy, whole brain radiotherapy) and a combination of both, for newly diagnosed brain metastases, and observed median survival times of 12-15 months, 8 months and 17 months, respectively. For recurrent metastases, survival times were around 6 months [104, 150]. Results for singular brain metastases are comparable with stereotactic radiosurgery .
A potential risk is growth of tumour cells by inoculation along the catheter pathway, which was seen by Ruge et al. in 6 out of 90 patients .
All in all, iodine-125 brachytherapy for metastases has become more popular again in recent years due to its radiobiological advantages and as it can be employed even after extensive percutaneous pre-irradiation , additionally biopsies are possible in the same session [154, 163].
Brachytherapy of pineal parenchymal tumours
Iodine-125 seeds (50-60Gy, 9-12cGy/h) have been used for recurrent pineoblastomas . A study of 18 patients (6-68 years) treated with 40-65Gy of permanent (11) or temporary (7) implants for primary pineal tumours or in a salvage situation has been published. 5 year overall actuarial survival rates of 100% for pineocytomas and of 78% for high-grade tumours have been reported. Complete remission rate was 72% and partial remission rate 28%. Maarouf et al. concluded that iodine-125 seeds are efficient and safe and an attractive alternative to microsurgery . All in all, iodine-125 brachytherapy treatment with a low dose rate seems to be an attractive, minimally invasive treatment option of these rare tumour entities of the pineal region.
Various indications of brachytherapy
One group implanted petroclival meningiomas . Treatment of meningiomas of the skull base and other localisations with permanent iodine-125 implants results in a complete response rate of 73-82% and a partial response rate of 18-27%, without early, and with rare late complications [166–170]. The treatment of parasellar-clival and globoid meningiomas with permanent implants showed a slow reduction in volume with no mortality . All these results are only of historical interest as seeds do not play a role in modern treatment of meningiomas.
Case reports present successful treatments of an example of bilateral blindness secondary to a recurrent, preirradiated hemangiopericytoma of the pituitary fossa , or of radiation-induced neoplasms . Even a clival chordoma  and other skull base tumours [175, 176] have been treated with an implantation of seeds, as well as locations that are a challenge for high-precision percutaneous radiotherapy [177, 178]. A case of Rosai-Dorfman disease of the central nervous system has been cured with brachytherapy , as well as child optic pathway gliomas . Craniopharyngiomas have been implanted without recurrences [181, 182] and recurrent medulloblastomas have been treated with iodine-125 brachytherapy . Sometimes iodine-125 implants may have a favourable long-lasting effect upon medically refractory seizures .
Side effects and complications
The following side effects and complications have been described in the literature: intracranial pressure and tumour expansion due to necrosis, severe oedema, cerebral artery occlusion, intracranial haemorrhage and subdural bleeding, headaches, nausea, vomiting, seizures, increased neurological deficits, abscesses, aseptic and septic meningitis, wound infections and dehiscence, delayed wound healing, scalp infections, cerebrospinal fluid leakage, long-term steroid dependency, progressive dementia, psychotic symptoms, facial pain, pulmonary embolism and others [12, 13, 22, 24, 45–47, 70, 81, 101, 107, 110, 114, 134, 137, 138, 155, 185]. Two cases of devastating strokes due to intracranial arterial occlusion have been reported . Tacke et al. found in 6 out of 13 children with low-grade hypothalamic gliomas signs of vasculopathy in magnetic resonance imaging, but only one of them revealed symptoms of intermittent cerebral ischemia .
No toxicity was reported in 92%, severe acute toxicity in 6%, life threatening in 1% and fatal in < 1% . All in all, the operative morbidity seems to be low (1.2-21.7%) [67, 79, 95, 107, 150, 155]. In patients with gliomas grade II, a combination of surgery plus iodine-125 brachytherapy had a morbidity of 27.8%, seed implantation alone of 6.4% . The perioperative mortality rate is max. 0.8-2.6% [4, 67, 68].
Radiation toxicity (oedema) has been reported mostly among patients treated with permanent implants [101, 104]. It occurs in 1.7-7.5% [68, 95, 96, 101, 104], although for tumours greater than 3.5 cm in diameter, it occurs in up to 18% of cases . Late radiation necrosis is a severe side effect which seems to occur in 40% of the low-dose-rate implantations and is correlated with total radiation dose, implanted activity and the velocity of tumour shrinkage. It can be avoided by the usage of temporary implants . A detailed analysis of patients with grade I and grade II gliomas undergoing low-activity iodine-125 brachytherapy has revealed as risk factors for radiogenic complications the volume of intratumoural 200Gy isodose and rapid tumour shrinkage of ≥ 50% of the volume in six months. A 200Gy-isodose-volume of < 4.5ml leads to < 3% radiogenic complications with a steep increase of the risk beyond this limit. For temporary implants with a reference dose of 60Gy, the risk for complications is < 3% if the treatment volume is ≤ 23 ml. Further factors affecting the toxicity rate examined are the overall treatment volume, the volume of the 60Gy isodose outside the target volume, reimplantation, the reference dose, the number of implanted seeds and a lobar tumour location . Other authors identified a target volume > 35ml and a permanent seed dose > 100Gy, or a temporary > 50Gy, as risk factors of complications . Evaluation of a brain necrosis after permanent seed implantation showed the necrotic area within the 100Gy isodose and damage to the blood-brain barrier within the 50Gy isodose . A long term analysis of Kreth et al. revealed a risk for radiogenic complications of about 9% for relatively small grade II gliomas (diameter < 4 cm) and a steep increase of complications (about 25%) for those harbouring larger tumours (≥ 4 cm). The increase of radiogenic complication rate beyond a critical threshold can be explained by the tissue effects of brachytherapy, such as the increase of capillary permeability in the vicinity of the high-dose zone and the exponential increase of the damaged capillary surface area product with the square of the radius of the high-dose zone . The risk of low-dose rate brachytherapy of low-grade gliomas should not be confused with the high frequency of complications (40-50%) after high-dose rate treatment of malignant gliomas. It remains difficult to elucidate, in which extent, additional external beam radiation, the often relatively large size of the treatment volume, and the applied high dose rate (in the range of 35-50cGy/h), have contributed to these high complication rates. Reoperation has been shown to be required in 0-72% because of treatment induced space occupying lesions, which occurred particularly after high dose rate brachytherapy 3-183 weeks after implantation [23, 25, 44–46, 53, 79, 81, 95, 101, 104, 105, 107, 109–114, 116–119, 123, 124, 127, 130, 132, 133, 135–139, 144, 150, 155, 185, 188, 189]. No correlation between implanted volume and need for reoperation has been found . However, there might be a correlation for the combination of percutaneous radiotherapy plus brachytherapy (64%), compared to percutaneous radiotherapy only (15%) , others found similar rates of around 30% for both groups . Histological findings (necrosis, tumour) at reoperation are not prognostic factors .
Percutaneous catheter derived brachytherapy may be associated with an increased incidence of extraneural metastatic gliomas of the scalp, skull, cervical nodes, etc. .
Quality of life
The quality of life in the majority of long-term survivors appears to be quite satisfactory [23, 44, 45, 193]. Comparing permanent and temporary implants, the KPS remained stable or improved in 85% and 58%. The neurological status emended in 87% and 67% . In another study the neurological function has improved in 30%, has shown no change in 43% and has declined in 27% . The KPS mostly improved in patients with astrocytomas II .
Summary and proposals for reduced side effects
In summary, to reduce the risk for side effects, temporary implants, dose rates around 10cGy/h and activities < 20mCi should be preferred, high dose zones > 150Gy should not be located within normal tissue and next to vessels, and volumes > 4 cm should not be implanted. If these guidelines are followed, then side effects are very rare .
Iodine-125 brachytherapy might be indicated in highly selected patients with recurrent brain tumours as a form of re-irradiation, low-grade gliomas, brain metastases with stable systemic disease and some other less common diagnoses, as it is a way to deliver an additional dose of localized radiation to malignant brain tumours while limiting radiation to the surrounding normal brain tissue . However, there is no strong randomized evidence that would justify the change of guidelines for any brain tumour entity. The side effects are rather rare. During follow-up, attention has to be paid to some special diagnostic features. In that case, iodine-125 seed implantation in brain tumours may lead to good survival rates and a decent quality of life.
- Holm HH, Stroyer I, Hansen H, Stadil F: ULTRASONICALLY GUIDED PERCUTANEOUS INTERSTITIAL IMPLANTATION OF I125 SEEDS IN CANCER-THERAPY. British Journal of Radiology 1981,54(644):665-670. 10.1259/0007-1285-54-644-665PubMedGoogle Scholar
- Matthews CME: HALF-LIFE OF IODINE-125. Physics in Medicine and Biology 1960,5(1):45-47. 10.1088/0031-9155/5/1/305PubMedGoogle Scholar
- Kim JH, Hilaris B: IODINE 125 SOURCE IN INTERSTITIAL TUMOR THERAPY - CLINICAL AND BIOLOGIC CONSIDERATIONS. American Journal of Roentgenology 1975,123(1):163-169.Google Scholar
- Mundinger F, Ostertag CB, Birg W, Weigel K: STEREOTACTIC TREATMENT OF BRAIN-LESIONS - BIOPSY, INTERSTITIAL RADIOTHERAPY (IR-192 AND I125) AND DRAINAGE PROCEDURES. Applied Neurophysiology 1980,43(3-5):198-204.PubMedGoogle Scholar
- Bernstein M, Gutin PH: Interstitial irradiation of brain tumors: a review. Neurosurgery 1981,9(6):741-750. 10.1227/00006123-198112000-00022PubMedGoogle Scholar
- Jani SK, Hitchon PW, Vangilder JC, Wen BC: NORMAL BRAIN IRRADIATION DURING STEREOTACTIC BRAIN IMPLANTS USING RADIOACTIVE I-125. Applied Neurophysiology 1987,50(1-6):310-313.PubMedGoogle Scholar
- Viola A, Major T, Julow J: Comparison of I-125 stereotactic brachytherapy and LINAC radiosurgery modalities based on physical dose distribution and radiobiological efficacy. Radiation Research 2006,165(6):695-702. 10.1667/RR3529.1PubMedGoogle Scholar
- Luxton G, Petrovich Z, Jozsef G, Nedzi LA, Apuzzo ML: Stereotactic radiosurgery: principles and comparison of treatment methods. Neurosurgery 1993,32(2):241-259. discussion 259 10.1227/00006123-199302000-00014PubMedGoogle Scholar
- Larson DA, Flickinger JC, Loeffler JS: The radiobiology of radiosurgery. Int J Radiat Oncol Biol Phys 1993,25(3):557-561. 10.1016/0360-3016(93)90080-FPubMedGoogle Scholar
- Larsson B: Radiobiological Fundamentals in Radiosurgery. Radiosurgery 1992, 3-14.Google Scholar
- Krishnaswamy V: DOSE DISTRIBUTION AROUND AN I125 SEED SOURCE IN TISSUE. Radiology 1978,126(2):489-491.PubMedGoogle Scholar
- Sneed PK, McDermott MW, Gutin PH: Interstitial brachytherapy procedures for brain tumors. Seminars in Surgical Oncology 1997,13(3):157-166. 10.1002/(SICI)1098-2388(199705/06)13:3<157::AID-SSU2>3.0.CO;2-6PubMedGoogle Scholar
- McDermott MW, Sneed PK, Gutin PH: Interstitial brachytherapy for malignant brain tumors. Seminars in Surgical Oncology 1998,14(1):79-87. 10.1002/(SICI)1098-2388(199801/02)14:1<79::AID-SSU10>3.0.CO;2-4PubMedGoogle Scholar
- Nath R, Anderson LL, Luxton G, Weaver KA, Williamson JF, Meigooni AS: DOSIMETRY OF INTERSTITIAL BRACHYTHERAPY SOURCES - RECOMMENDATIONS OF THE AAPM RADIATION-THERAPY COMMITTEE TASK GROUP NO 43. Medical Physics 1995,22(2):209-234. 10.1118/1.597458PubMedGoogle Scholar
- Sewchand W, Drzymala RE, Amin PP, Salcman M, Salazar OM: RADIATION CONTROL IN THE INTENSIVE-CARE UNIT FOR HIGH-INTENSITY IR-192 BRAIN IMPLANTS. Neurosurgery 1987,20(4):584-588. 10.1227/00006123-198704000-00013PubMedGoogle Scholar
- Kreth FW, Thon N, Siefert A, Tonn JC: The place of interstitial brachytherapy and radiosurgery for low-grade gliomas. Adv Tech Stand Neurosurg 2010, 35: 183-212. 10.1007/978-3-211-99481-8_7PubMedGoogle Scholar
- Mundinger F: [Stereotaxic interstitial therapy of non-resectable intracranial tumors with iridium-192 and iodine-125]. Strahlentherapie [Sonderb] 1981, 76: 90-112.Google Scholar
- Fike JR, Cann CE, Phillips TL, Bernstein M, Gutin PH, Turowski K, Weaver KA, Davis RL, Higgins RJ, Dasilva V: Radiation Brain-Damage Induced by Interstitial I125 Sources - a Canine Model Evaluated by Quantitative Computed-Tomography. Neurosurgery 1985,16(4):530-537. 10.1227/00006123-198504000-00015PubMedGoogle Scholar
- Groothuis DR, Wright DC, Ostertag CB: The Effect of I-125 Interstitial Radiotherapy on Blood-Brain-Barrier Function in Normal Canine Brain. J Neurosurg 1987,67(6):895-902. 10.3171/jns.1987.67.6.0895PubMedGoogle Scholar
- Ostertag CB: Brachytherapy - Interstitial Implant Radiosurgery. Acta Neurochir 1993, 79-84.Google Scholar
- Meli JA, Dicker CS, Schulz RJ: COMPUTER-APPLICATIONS TO RADIOACTIVE-SEED - BRAIN-TUMOR IMPLANTS. Computerized Medical Imaging and Graphics 1989,13(3):269-274. 10.1016/0895-6111(89)90133-XPubMedGoogle Scholar
- Hosobuchi Y, Phillips TL, Stupar TA, Gutin PH: INTERSTITIAL BRACHYTHERAPY OF PRIMARY BRAIN-TUMORS - PRELIMINARY-REPORT. J Neurosurg 1980,53(5):613-617. 10.3171/jns.1980.53.5.0613PubMedGoogle Scholar
- Gutin PH, Prados MD, Phillips TL, Wara WM, Larson DA, Leibel SA, Sneed PK, Levin VA, Weaver KA, Silver P, et al.: EXTERNAL IRRADIATION FOLLOWED BY AN INTERSTITIAL HIGH-ACTIVITY I-125 IMPLANT BOOST IN THE INITIAL TREATMENT OF MALIGNANT GLIOMAS - NCOG STUDY 6G-82-2. International Journal of Radiation Oncology Biology Physics 1991,21(3):601-606. 10.1016/0360-3016(91)90676-UGoogle Scholar
- Laperriere NJ, Leung PMK, McKenzie S, Milosevic M, Wong S, Glen J, Pintilie M, Bernstein M: Randomized study of brachytherapy in the initial management of patients with malignant astrocytoma. International Journal of Radiation Oncology Biology Physics 1998,41(5):1005-1011. 10.1016/S0360-3016(98)00159-XGoogle Scholar
- Scharfen CO, Sneed PK, Wara WM, Larson DA, Phillips TL, Prados MD, Weaver KA, Malec M, Acord P, Lamborn KR, et al.: HIGH-ACTIVITY I-125 INTERSTITIAL IMPLANT FOR GLIOMAS. International Journal of Radiation Oncology Biology Physics 1992,24(4):583-591. 10.1016/0360-3016(92)90702-JGoogle Scholar
- Kumar PP, Good RR, Patil AA, Leibrock LG: PERMANENT HIGH-ACTIVITY I-125 IN THE MANAGEMENT OF PETROCLIVAL MENINGIOMAS - CASE-REPORTS. Neurosurgery 1989,25(3):436-442. 10.1227/00006123-198909000-00019PubMedGoogle Scholar
- Ling CC: GOLD-198 PALLADIUM-103 AND IODINE-125 PERMANENT IMPLANTS RADIOBIOPHYSICAL CONSIDERATIONS. Medical Physics (Woodbury) 1991,18(3):637.Google Scholar
- Bauerkirpes B, Sturm V, Schlegel W, Lorenz WJ: COMPUTERIZED OPTIMIZATION OF I125 IMPLANTS IN BRAIN-TUMORS. International Journal of Radiation Oncology Biology Physics 1988,14(5):1013-1023. 10.1016/0360-3016(88)90027-2Google Scholar
- Meningher H, Benary V, Chaitchick S, Akselrod S: A PLANNING METHOD FOR I-125 IMPLANTS IN CANCER-THERAPY. Physics in Medicine and Biology 1990,35(12):1633-1640. 10.1088/0031-9155/35/12/004PubMedGoogle Scholar
- Rosenow UF, Findlay PA, Wright DC: THE NCI-ATLAS OF DOSE DISTRIBUTIONS FOR REGULAR I-125 BRAIN IMPLANTS. Radiotherapy and Oncology 1987,10(2):127-139. 10.1016/S0167-8140(87)80055-5PubMedGoogle Scholar
- Saw CB, Suntharalingam N, Ayyangar KM, Tupchong L: DOSIMETRIC CONSIDERATIONS OF STEREOTACTIC BRAIN IMPLANTS. International Journal of Radiation Oncology Biology Physics 1989,17(4):887-891. 10.1016/0360-3016(89)90083-7Google Scholar
- Weaver K, Smith V, Lewis JD, Lulu B, Barnett CM, Leibel SA, Gutin P, Larson D, Phillips T: A CT-BASED COMPUTERIZED TREATMENT PLANNING SYSTEM FOR I-125 STEREOTACTIC BRAIN IMPLANTS. International Journal of Radiation Oncology Biology Physics 1990,18(2):445-454. 10.1016/0360-3016(90)90114-YGoogle Scholar
- Zamorano L, Dujovny M, Malik G, Yakar D, Mehta B: MULTIPLANAR CT-GUIDED STEREOTAXIS AND I125 INTERSTITIAL RADIOTHERAPY - IMAGE-GUIDED TUMOR VOLUME ASSESSMENT, PLANNING, DOSIMETRIC CALCULATIONS, STEREOTACTIC BIOPSY AND IMPLANTATION OF REMOVABLE CATHETERS. Applied Neurophysiology 1987,50(1-6):281-286.PubMedGoogle Scholar
- Ahmad M, Fontenla DP, Tsao STC, Chui CS, Reiff JE, Anderson LL, Huang DYC, Schell MC: DIODE DOSIMETRY OF MODEL-6711 AND MODEL-6712 I-125 SEEDS IN A WATER PHANTOM. Medical Physics 1992,19(2):391-399. 10.1118/1.596872PubMedGoogle Scholar
- Dale RG: SOME THEORETICAL DERIVATIONS RELATING TO THE TISSUE DOSIMETRY OF BRACHYTHERAPY NUCLIDES, WITH PARTICULAR REFERENCE TO I125. Medical Physics 1983,10(2):176-183. 10.1118/1.595297PubMedGoogle Scholar
- Hartmann GH, Schlegel W, Scharfenberg H: THE 3-DIMENSIONAL DOSE DISTRIBUTION OF I-125 SEEDS IN TISSUE. Physics in Medicine and Biology 1983,28(6):693-699. 10.1088/0031-9155/28/6/009PubMedGoogle Scholar
- Krishnaswamy V: DOSE TABLES FOR I125 SEED IMPLANTS. Radiology 1979,132(3):727-730.PubMedGoogle Scholar
- Mainegra E, Capote R, Lopez E: Dose rate constants for I-125, Pd-103, Ir-192 and Yb-169 brachytherapy sources: an EGS4 Monte Carlo study. Physics in Medicine and Biology 1998,43(6):1557-1566. 10.1088/0031-9155/43/6/014PubMedGoogle Scholar
- Mobit P, Badragan I: An evaluation of the AAPM-TG43 dosimetry protocol for I-125 brachytherapy seed. Physics in Medicine and Biology 2004.,49(14): DOI 10.1088/0031-9155/1049/1014/1010PII S0031-9155(1004)72823-72827Google Scholar
- Rodriguez EAV, Alcon EPQ, Rodriguez ML, Gutt F, de Almeida E: Dosimetric parameters estimation using PENELOPE Monte-Carlo simulation code: Model 6711 a I-125 brachytherapy seed. Applied Radiation and Isotopes 2005,63(1):41-48. 10.1016/j.apradiso.2005.02.004PubMedGoogle Scholar
- Anderson LL, Harrington PJ, Osian AD, Arbit E, Leibel SA, Malkin MG: A VERSATILE METHOD FOR PLANNING STEREOTAXIC BRAIN IMPLANTS. Medical Physics 1993,20(5):1457-1464. 10.1118/1.597109PubMedGoogle Scholar
- Kall BA, Kelly PJ, Stiving SO, Goerss SJ: Preoperative computer-assisted simulation of interstitial iodine-125 source placements into CNS lesion volumes. Stereotactic and Functional Neurosurgery 1992,59(1-4):205.Google Scholar
- Bernstein M, Lumley M, Davidson G, Laperriere N, Leung P: INTRACRANIAL ARTERIAL-OCCLUSION ASSOCIATED WITH HIGH-ACTIVITY I-125 BRACHYTHERAPY FOR GLIOBLASTOMA. J Neuro-Oncol 1993,17(3):253-260. 10.1007/BF01049980Google Scholar
- Leibel S, Gutin P, Wara W, Silver P, Hannigan J, Lamb S, Weaver K, Phillips T: SURVIVAL AND QUALITY OF LIFE FOLLOWING INTERSTITIAL IMPLANTATION OF REMOVABLE HIGH-ACTIVITY IODINE-125 SOURCES FOR RECURRENT MALIGNANT GLIOMAS. International Journal of Radiation Oncology, Biology, Physics 1988,15(SUPPL. 1):155-156.Google Scholar
- Leibel SA, Gutin PH, Wara WM, Silver PS, Larson DA, Edwards MSB, Lamb SA, Ham B, Weaver KA, Barnett C, et al.: SURVIVAL AND QUALITY OF LIFE AFTER INTERSTITIAL IMPLANTATION OF REMOVABLE HIGH-ACTIVITY I-125 SOURCES FOR THE TREATMENT OF PATIENTS WITH RECURRENT MALIGNANT GLIOMAS. International Journal of Radiation Oncology Biology Physics 1989,17(6):1129-1139. 10.1016/0360-3016(89)90518-XGoogle Scholar
- Willis BK, Heilbrun MP, Sapozink MD, McDonald PR: STEREOTACTIC INTERSTITIAL BRACHYTHERAPY OF MALIGNANT ASTROCYTOMAS WITH REMARKS ON POSTIMPLANTATION COMPUTED TOMOGRAPHIC APPEARANCE. Neurosurgery 1988,23(3):348-354. 10.1227/00006123-198809000-00011PubMedGoogle Scholar
- Wright DC, Findlay P, Rosenow U, Orr K, Miller R, Harrington F, Kinsella T: IODINE-125 INTERSTITIAL BRACHYTHERAPY FOR PRIMARY MALIGNANT BRAIN TUMORS A PHASE I-II STUDY. International Journal of Radiation Oncology, Biology, Physics 1987,13(SUPPL. 1):148-149.Google Scholar
- Schupak KD, Fass D, Malkin M, Arbit E, Anderson L, Lindsley K, Leibel S: RELATIONSHIP OF THE PATTERNS OF RECURRENCE TO THE TECHNICAL ACCURACY OF STEREOTACTIC INTERSTITIAL IMPLANTATION FOR HIGH GRADE GLIOMAS. International Journal of Radiation Oncology, Biology, Physics 1991,21(SUPPL. 1):221-222.Google Scholar
- Eddy M, Deutsch M, Selker R: QUALITY ASSURANCE FOR IODINE-125 BRAIN IMPLANTS PROGRAM DESCRIPTION AND PRELIMINARY RESULTS. Medical Physics (Woodbury) 1991,18(3):605.Google Scholar
- Dale RG: THE APPLICATION OF THE LINEAR-QUADRATIC DOSE-EFFECT EQUATION TO FRACTIONATED AND PROTRACTED RADIOTHERAPY. British Journal of Radiology 1985,58(690):515-528. 10.1259/0007-1285-58-690-515PubMedGoogle Scholar
- Dale RG: RADIOBIOLOGICAL ASSESSMENT OF PERMANENT IMPLANTS USING TUMOR REPOPULATION FACTORS IN THE LINEAR-QUADRATIC MODEL. British Journal of Radiology 1989,62(735):241-244. 10.1259/0007-1285-62-735-241PubMedGoogle Scholar
- Dale RG, Jones B, Coles IP: EFFECT OF TUMOR SHRINKAGE ON THE BIOLOGICAL EFFECTIVENESS OF PERMANENT BRACHYTHERAPY IMPLANTS. British Journal of Radiology 1994,67(799):639-645. 10.1259/0007-1285-67-799-639PubMedGoogle Scholar
- Gaspar LE, Zamorano LJ, Shamsa F, Fontanesi J, Ezzell GE, Yakar DA: Permanent (125)iodine implants for recurrent malignant gliomas. International Journal of Radiation Oncology Biology Physics 1999,43(5):977-982. 10.1016/S0360-3016(98)00494-5Google Scholar
- Yaes RJ: Late normal tissue injury from permanent interstitial implants. International Journal of Radiation Oncology Biology Physics 2001,49(4):1163-1169. 10.1016/S0360-3016(00)01425-5Google Scholar
- Julow J, Szeifert GT, Balint K, Nyary I, Nemes Z: The role of microglia/macrophage system in the tissue response to I-125 interstitial brachytherapy of cerebral gliomas. Neurological Research 2007,29(3):233-238. 10.1179/016164107X158875PubMedGoogle Scholar
- Janzer RC, Kleihues P, Ostertag CB: Early and Late Effects on the Normal Dog Brain of Permanent Interstitial Ir-192 Irradiation. Acta Neuropathol 1986,70(2):91-102. 10.1007/BF00691426PubMedGoogle Scholar
- Lehnert S, Reniers B, Verhaegen F: Relative biologic effectiveness in terms of tumor response of I-125 implants compared with Co-60 gamma rays. International Journal of Radiation Oncology Biology Physics 2005,63(1):224-229. 10.1016/j.ijrobp.2005.05.009Google Scholar
- Ling CC, Li WX, Anderson LL: THE RELATIVE BIOLOGICAL EFFECTIVENESS OF I-125 AND PD-103. International Journal of Radiation Oncology Biology Physics 1995,32(2):373-378. 10.1016/0360-3016(95)00530-CGoogle Scholar
- Zeitz L, Kim SH, Kim JH: RELATIVE BIOLOGICAL EFFECTIVENESS (RBE) OF X-RAYS SIMULATING RADIATION FROM ENCAPSULATED I125 SOURCES. Radiation Research 1976,67(3):549-549.Google Scholar
- Da Silva VF, Gutin PH, Deen DF, Weaver KA: RELATIVE BIOLOGICAL EFFECTIVENESS OF IODINE-125 SOURCES IN A MURINE BRACHYTHERAPY MODEL. International Journal of Radiation Oncology, Biology, Physics 1984,10(11):2109-2112. 10.1016/0360-3016(84)90209-8PubMedGoogle Scholar
- Siddiqi SN, Provias J, Laperriere N, Bernstein M: Effects of iodine-125 brachytherapy on the proliferative capacity and histopathological features of glioblastoma recurring after initial therapy. Neurosurgery 1997,40(5):910-917. 10.1097/00006123-199705000-00005PubMedGoogle Scholar
- Cron GO, Beghein N, Crokart N, Chavee E, Bernard S, Vynckier S, Scalliet P, Gallez B: Changes in the tumor microenvironment during low-dose-rate permanent seed implantation iodine-125 brachytherapy. International Journal of Radiation Oncology Biology Physics 2005,63(4):1245-1251. 10.1016/j.ijrobp.2005.07.971Google Scholar
- Julow J, Szeifert GT, Balint K, Nyary I, Nemes Z: Tissue response to iodine-125 interstitial brachytherapy of cerebral gliomas. Prog Neurol Surg 2007, 20: 312-323.PubMedGoogle Scholar
- Fike JR, Cann CE, Bernstein M, Davis RL, Phillips TL, Gutin PH, Weaver KA: RADIATION-DAMAGE TO THE CANINE BRAIN AFTER I-125 IMPLANTATION. Radiation Research 1982,91(2):370-370.Google Scholar
- Kunz M, Thon N, Eigenbrod S, Hartmann C, Geisler J, Kretzschmar H, von Deimling A, Popperl G, Tonn J, Kreth F: Hot Spots in 18 Fet-Pet Delineate Malignant Tumor Parts within Suspected Who Grade Ii Glioma. Neuro-Oncology 2010, 12: 12-12.Google Scholar
- Kunz M, Thon N, Eigenbrod S, Hartmann C, Egensperger R, Herms J, Geisler J, la Fougere C, Lutz J, Linn J, et al.: Hot spots in dynamic (18)FET-PET delineate malignant tumor parts within suspected WHO grade II gliomas. Neuro Oncol 2011,13(3):307-316. 10.1093/neuonc/noq196PubMed CentralPubMedGoogle Scholar
- Kreth FW, Faist M, Grau S, Ostertag CB: Interstitial I-125 radiosurgery of supratentorial De Novo WHO grade 2 astrocytorna and oligoastrocytorna in adults - Long-term results and prognostic factors. Cancer 2006,106(6):1372-1381. 10.1002/cncr.21750PubMedGoogle Scholar
- Kreth FW, Faist M, Warnke PC, Rossner R, Volk B, Ostertag CB: INTERSTITIAL RADIOSURGERY OF LOW-GRADE GLIOMAS. J Neurosurg 1995,82(3):418-429. 10.3171/jns.1995.82.3.0418PubMedGoogle Scholar
- Findlay PA, Wright DC, Harrington FS, Miller RW, Glatstein E: IODINE-125 INTERSTITIAL BRACHYTHERAPY FOR PRIMARY MALIGNANT BRAIN TUMORS TECHNICAL ASPECTS OF TREATMENT PLANNING AND IMPLANTATION METHODS. International Journal of Radiation Oncology, Biology, Physics 1984,10(SUPPL. 2):93-94.Google Scholar
- Gutin PH, Phillips TL, Wara WM, Leibel SA, Hosobuchi Y, Levin VA, Weaver KA, Lamb S: BRACHYTHERAPY OF RECURRENT MALIGNANT BRAIN-TUMORS WITH REMOVABLE HIGH-ACTIVITY I125 SOURCES. J Neurosurg 1984,60(1):61-68. 10.3171/jns.1984.60.1.0061PubMedGoogle Scholar
- Julow J, Major T, Emri M, Valalik I, Sagi S, Mangel L, Nemeth G, Tron L, Varallyay G, Solymosi D, et al.: The application of image fusion in stereotactic brachytherapy of brain tumours. Acta Neurochir 2000,142(11):1253-1258. 10.1007/s007010070022PubMedGoogle Scholar
- Peraud A, Goetz C, Siefert A, Tonn JC, Kreth FW: Interstitial iodine-125 radiosurgery alone or in combination with microsurgery for pediatric patients with eloquently located low-grade glioma: a pilot study. Childs Nervous System 2007,23(1):39-46.Google Scholar
- Ten Haken RK, Diaz RF, McShan DL, Fraass BA, Taren JA, Hood TW: FROM MANUAL TO 3-D COMPUTERIZED TREATMENT PLANNING FOR IODINE-125 STEREOTACTIC BRAIN IMPLANTS. International Journal of Radiation Oncology, Biology, Physics 1988,15(2):467-480. 10.1016/S0360-3016(98)90032-3PubMedGoogle Scholar
- Viola A, Major T, Julow J: The importance of postoperative CT image fusion verification of stereotactic interstitial irradiation for brain tumors. International Journal of Radiation Oncology Biology Physics 2004,60(1):322-328. 10.1016/j.ijrobp.2004.04.045Google Scholar
- Knuefermann H, Wannenmacher M, Sommerkamp H, Fiedler L, Brobmann G: INDICATIONS AND LIMITS OF INTERSTITIAL RADIO THERAPY WITH IODINE-125 SEEDS. J Cancer Res Clin 1984,107(SUPPL):S60.Google Scholar
- Loeffler JS, Kooy HM, Wen PY, Fine HA, Cheng CW, Mannarino EG, Tsai JS, Alexander E: THE TREATMENT OF RECURRENT BRAIN METASTASES WITH STEREOTACTIC RADIOSURGERY. Journal of Clinical Oncology 1990,8(4):576-582.PubMedGoogle Scholar
- Healey EA, Shamberger RC, Grier HE, Loeffler JS, Tarbell NJ: A 10-YEAR EXPERIENCE OF PEDIATRIC BRACHYTHERAPY. International Journal of Radiation Oncology Biology Physics 1995,32(2):451-455. 10.1016/0360-3016(95)00520-9Google Scholar
- Stowe SM, Littman P, Wara W, Raney RB, Tefft M: THE USE OF IMPLANTATION IN CHILDHOOD TUMORS - THE EXPERIENCE OF CHILDRENS CANCER STUDY-GROUP MEMBER INSTITUTIONS. American Journal of Clinical Oncology-Cancer Clinical Trials 1982,5(2):129-129.Google Scholar
- Bernstein M, Laperriere N, Glen J, Leung P, Thomason C, Landon AE: BRACHYTHERAPY FOR RECURRENT MALIGNANT ASTROCYTOMA. International Journal of Radiation Oncology Biology Physics 1994,30(5):1213-1217.Google Scholar
- Frank F, Fabrizi AP, Gaist G, Frankricci R, Piazzi M, Spagnolli F: LATE CONSIDERATIONS IN THE TREATMENT OF LOW-GRADE MALIGNANCY CEREBRAL-TUMORS WITH I-125 BRACHYTHERAPY. Applied Neurophysiology 1987,50(1-6):302-309.PubMedGoogle Scholar
- Larson DA, Gutin PH, Leibel SA, Phillips TL, Sneed PK, Wara WM: STEREOTAXIC IRRADIATION OF BRAIN-TUMORS. Cancer 1990,65(3):792-799. 10.1002/1097-0142(19900201)65:3+<792::AID-CNCR2820651327>3.0.CO;2-PPubMedGoogle Scholar
- Voges J, Gaus C, Schlegel W, Pastyr O, Wowra B, Sturm V: INTERSTITIAL IRRADIATION OF A LARGE, LOW-GRADE EPENDYMOMA WITH STEREOTAXICALLY IMPLANTED I-125 SEEDS. Acta Neurochir 1993,122(1-2):127-129. 10.1007/BF01446999PubMedGoogle Scholar
- Mundinger F, Braus DF, Krauss JK, Birg W: LONG-TERM OUTCOME OF 89 LOW-GRADE BRAIN-STEM GLIOMAS AFTER INTERSTITIAL RADIATION-THERAPY. J Neurosurg 1991,75(5):740-746. 10.3171/jns.1991.75.5.0740PubMedGoogle Scholar
- Julow J, Viola A, Major T, Valalik I, Sagi S, Mangel L, Kovacs BR, Repa I, Bajzik G, Zoltan TN, et al.: Iodine-125 brachytherapy of brain stem tumors. Strahlenther Onkol 2004,180(7):449-454.PubMedGoogle Scholar
- Wowra B, Schmitt HP, Sturm V: INCIDENCE OF LATE RADIATION NECROSIS WITH TRANSIENT MASS EFFECT AFTER INTERSTITIAL LOW-DOSE RATE RADIOTHERAPY FOR CEREBRAL GLIOMAS. Acta Neurochir 1989,99(3-4):104-108. 10.1007/BF01402316PubMedGoogle Scholar
- Julow J, Kolumban Z, Viola A, Major T, Kolumban G: Prediction of volumetric change in the "triple ring" caused by glioma I-125 brachytherapy. Neuro-Oncology 2008,10(4):583-592. 10.1215/15228517-2008-027PubMed CentralPubMedGoogle Scholar
- Voges J, Herholz K, Holzer T, Wurker M, Bauer B, Pietrzyk U, Treuer H, Schroder R, Sturm V, Heiss WD: C-11-methionine and F-18-2-fluorodeoxy-glucose positron emission tomography: A tool for diagnosis of cerebral glioma and monitoring after brachytherapy with I-125 seeds. Stereotactic and Functional Neurosurgery 1997,69(1-4):129-135. 10.1159/000099864PubMedGoogle Scholar
- Wurker M, Herholz K, Voges J, Pietrzyk U, Treuer H, Bauer B, Sturm V, Heiss WD: Glucose consumption and methionine uptake in low-grade gliomas after iodine-125 brachytherapy. European Journal of Nuclear Medicine 1996,23(5):583-586. 10.1007/BF00833397PubMedGoogle Scholar
- Aiken AH, Chang SM, Larson D, Butowski N, Cha S: LONGITUDINAL MAGNETIC RESONANCE IMAGING FEATURES OF GLIOBLASTOMA MULTIFORME TREATED WITH RADIOTHERAPY WITH OR WITHOUT BRACHYTHERAPY. International Journal of Radiation Oncology Biology Physics 2008,72(5):1340-1346. 10.1016/j.ijrobp.2008.02.078Google Scholar
- Aarsen FK, Paquier PF, Reddingius RE, Streng IC, Arts WF, Evera-Preesman M, Catsman-Berrevoets CE: Functional outcome after low-grade astrocytoma treatment in childhood. Cancer 2006,106(2):396-402. 10.1002/cncr.21612PubMedGoogle Scholar
- Steinbok P: Management and outcome of low-grade astrocytomas of the midline in children: A retrospective review. Neurosurgery 1994,35(2):342-343.PubMedGoogle Scholar
- Sutton LN, Molloy PT, Sernyak H, Goldwein J, Phillips PL, Rorke LB, Moshang T Jr, Lange B, Packer RJ: Long-term outcome of hypothalamic/chiasmatic astrocytomas in children treated with conservative surgery. J Neurosurg 1995,83(4):583-589. 10.3171/jns.1995.83.4.0583PubMedGoogle Scholar
- Etou A, Mundinger F, Mohadjer M, Birg W: STEREOTACTIC INTERSTITIAL IRRADIATION OF DIENCEPHALIC TUMORS WITH IR-192 AND I-125 - 10 YEARS FOLLOW-UP AND COMPARISON WITH OTHER TREATMENTS. Childs Nervous System 1989,5(3):140-143. 10.1007/BF00272114Google Scholar
- Herrera EJ, Viano JC, Gomez JM, Surur A, Suarez JC: Interstitial stereotactic radiosurgery of pilocytic astrocytomas in paediatric patients. Acta Neurochir 2007,149(9):887-896. 10.1007/s00701-007-1237-7PubMedGoogle Scholar
- Ostertag CB, Kreth FW: I-125 INTERSTITIAL IRRADIATION FOR CEREBRAL GLIOMAS. Acta Neurochir 1992,119(1-4):53-61. 10.1007/BF01541782PubMedGoogle Scholar
- Kreth FW, Faist M, Rossner R, Birg W, Volk B, Ostertag CB: The risk of interstitial radiotherapy of low-grade gliomas. Radiotherapy and Oncology 1997,43(3):253-260. 10.1016/S0167-8140(97)01948-8PubMedGoogle Scholar
- Vitaz TW, Warnke PC, Tabar V, Gutin PH: Brachytherapy for brain tumors. J Neurooncol 2005,73(1):71-86. 10.1007/s11060-004-2352-4PubMedGoogle Scholar
- Julow J, Viola A, Balint K, Szeifert GT: Image fusion-guided stereotactic iodine-125 interstitial irradiation of inoperable and recurrent gliomas. Prog Neurol Surg 2007, 20: 303-311.PubMedGoogle Scholar
- Kreth FW, Faist M, Rossner R, Volk B, Ostertag CB: Supratentorial world health organization grade 2 astrocytomas and oligoastrocytomas - A new pattern of prognostic factors. Cancer 1997,79(2):370-379. 10.1002/(SICI)1097-0142(19970115)79:2<370::AID-CNCR21>3.0.CO;2-XPubMedGoogle Scholar
- Kreth FW, Warnke PC, Ostertag CB: INTERSTITIAL RADIOSURGERY IN TREATMENT OF LOW-GRADE GLIOMAS. Nervenarzt 1993,64(10):633-639.PubMedGoogle Scholar
- Mehrkens JH, Kreth FW, Muacevic A, Ostertag CB: Long term course of WHO grade II astrocytomas of the Insula of Reil after I-125 interstitial irradiation. J Neurol 2004,251(12):1455-1464. 10.1007/s00415-004-0561-6PubMedGoogle Scholar
- Schnell O, Scholler K, Ruge M, Siefert A, Tonn JC, Kreth FW: Surgical resection plus stereotactic I-125 brachytherapy in adult patients with eloquently located supratentorial WHO grade II glioma - Feasibility and outcome of a combined local treatment concept. J Neurol 2008,255(10):1495-1502. 10.1007/s00415-008-0948-xPubMedGoogle Scholar
- Warnke PC, Berlis A, Weyerbrock A, Ostertag CB: Significant reduction of seizure incidence and increase of benzodiazepine receptor density after interstitial radiosurgery in low-grade gliomas. Acta Neurochir Suppl 1997, 68: 90-92.PubMedGoogle Scholar
- Kreth FW, Warnke PC, Ostertag CB: INTERSTITIAL IMPLANT RADIOSURGERY FOR CEREBRAL METASTASES. Acta Neurochir 1993, 112-114.Google Scholar
- Scerrati M, Montemaggi P, Iacoangeli M, Roselli R, Rossi GF: INTERSTITIAL BRACHYTHERAPY FOR LOW-GRADE CEREBRAL GLIOMAS - ANALYSIS OF RESULTS IN A SERIES OF 36 CASES. Acta Neurochir 1994,131(1-2):97-105. 10.1007/BF01401459PubMedGoogle Scholar
- Suchorska B, Ruge M, Treuer H, Sturm V, Voges J: Stereotactic brachytherapy of low-grade cerebral glioma after tumor resection. Neuro Oncol 2011,13(10):1133-1142. 10.1093/neuonc/nor100PubMed CentralPubMedGoogle Scholar
- Bernstein M, Laperriere N, Leung P, McKenzie S: INTERSTITIAL BRACHYTHERAPY FOR MALIGNANT BRAIN-TUMORS - PRELIMINARY-RESULTS. Neurosurgery 1990,26(3):371-380. 10.1227/00006123-199003000-00001PubMedGoogle Scholar
- Clark WC, Fontanesi J, Patterson K, Kun L, Robertson JT: CT-GUIDED STEREOTACTIC BRACHYTHERAPY WITH IODINE-125 SEEDS FOR INITIAL TREATMENT OF MALIGNANT ASTROCYTOMA AND GLIOBLASTOMA MULTIFORME. Southern Medical Journal 1991,84(9):2S42-42S43.Google Scholar
- Gutin P, Wara W, Larson D, Leibel S, Prados M, Levin V, Sneed P, Weaver K, Silver P, et al.: STEREOTAXIC INTERSTITIAL IODINE-125 BOOST IN THE INITIAL MANAGEMENT OF MALIGNANT GLIOMAS. International Journal of Radiation Oncology, Biology, Physics 1990,19(SUPPL. 1):204.Google Scholar
- Gutin PH, Leibel SA, Wara WM, Choucair A, Levin VA, Philips TL, Silver P, Dasilva V, Edwards MSB, Davis RL, et al.: RECURRENT MALIGNANT GLIOMAS - SURVIVAL FOLLOWING INTERSTITIAL BRACHYTHERAPY WITH HIGH-ACTIVITY I-125 SOURCES. J Neurosurg 1987,67(6):864-873. 10.3171/jns.1987.67.6.0864PubMedGoogle Scholar
- Leibel S, Gutin P, Phillips T, Wara W, Choucair A, Weaver K, Lamb S, Silver P, Barnett C: IMPROVED SURVIVAL FOLLOWING INTERSTITIAL IMPLANTATION OF REMOVABLE HIGH-ACTIVITY IODINE-125 SOURCES FOR MALIGNANT RECURRENT GLIOMAS. International Journal of Radiation Oncology, Biology, Physics 1986,12(SUPPL. 1):146.Google Scholar
- Prados MD, Gutin PH, Phillips TL, Wara WM, Sneed PK, Larson DA, Lamb SA, Ham B, Malec MK, Wilson CB: INTERSTITIAL BRACHYTHERAPY FOR NEWLY DIAGNOSED PATIENTS WITH MALIGNANT GLIOMAS - THE UCSF EXPERIENCE. International Journal of Radiation Oncology Biology Physics 1992,24(4):593-597. 10.1016/0360-3016(92)90703-KGoogle Scholar
- Scharfen CO, Sneed PK, Wara WM, Larson DA, Phillips TL, Weaver KA, Prados MD, Gutin PH: STEREOTAXIC IODINE-125 BRAIN IMPLANTS FOR MALIGNANT GLIOMAS. International Journal of Radiation Oncology, Biology, Physics 1991,21(SUPPL. 1):119.Google Scholar
- Sneed PK, Gutin PH, Stauffer PR, Phillips TL, Prados MD, Weaver KA, Suen S, Lamb SA, Ham B, Ahn DK, et al.: THERMORADIOTHERAPY OF RECURRENT MALIGNANT BRAIN-TUMORS. International Journal of Radiation Oncology Biology Physics 1992,23(4):853-861. 10.1016/0360-3016(92)90659-6Google Scholar
- Yakar D, Zamorano L, Dujovny M, Sheehan M, Kim JH: Interstitial iodine-125 irradiation for malignant brain tumors: Advantage of permanent implant (PI) over temporary implants (TI). International Journal of Radiation Oncology Biology Physics 1992,24(SUPPL. 1):143.Google Scholar
- Fernandez P, Zamorano L, Gaspar L, Yakar D, Heilbrun LK: Permanent 125I implant therapy with concurrent external beam radiation in the up-front treatment of malignant gliomas. Stereotactic and Functional Neurosurgery 1994,63(1-4):287-288.Google Scholar
- Fernandez PM, Zamorano L, Yakar D, Gaspar L, Warmelink C: PERMANENT I-125 IMPLANTS IN THE UP-FRONT TREATMENT OF MALIGNANT GLIOMAS. Neurosurgery 1995,36(3):467-473. 10.1227/00006123-199503000-00004PubMedGoogle Scholar
- Fontanesi J, Clark WC, Weir A, Barry A, Kumar P, Miller A, Eddy T, Tai D, Kun LE: INTERSTITIAL I-125 AND CONCOMITANT CISPLATIN FOLLOWED BY HYPERFRACTIONATED EXTERNAL-BEAM IRRADIATION FOR MALIGNANT SUPRATENTORIAL GLIOMA - PRELIMINARY EXPERIENCE AT THE UNIVERSITY-OF-TENNESSEE, MEMPHIS. American Journal of Clinical Oncology-Cancer Clinical Trials 1993,16(5):412-417.Google Scholar
- Gaspar L, Zamorano L, Garcia L, Shamsa F, Warmelink C, Yakar D: Malignant gliomas: Permanent iodine-125 implants. International Journal of Radiation Oncology Biology Physics 1994,30(SUPPL 1):295.Google Scholar
- Schwarz SB, Siefert A, Ganswindt U, Kunz M, Kreth FW, Tonn JC, Belka C: The combination of percutaneous radiotherapy and (125)iodine-seed-implantation within the framework of multi model therapy concepts for cerebral tumours. Strahlentherapie Und Onkologie 2009, 185: 84-84.Google Scholar
- Videtic GMM, Gaspar LE, Zamorano L, Fontanesi J, Levin KJ, Kupsky WJ, Tekyi-Mensah S: Use of the RTOG recursive partitioning analysis to validate the benefit of iodine-125 implants in the primary treatment of malignant gliomas. International Journal of Radiation Oncology Biology Physics 1999,45(3):687-692. 10.1016/S0360-3016(99)00244-8Google Scholar
- Videtic GMM, Gaspar LE, Zamorano L, Stitt LW, Fontanesi J, Levin KJ: Implant volume as a prognostic variable in brachytherapy decision-making for malignant gliomas stratified by the RTOG recursive partitioning analysis. International Journal of Radiation Oncology Biology Physics 2001,51(4):963-968. 10.1016/S0360-3016(01)01746-1Google Scholar
- Zamorano L, Gaspar L, Garcia L, Yakar D, Shamsa F, Buciuc R, Diaz FG: PERMANENT I-125 IMPLANT IN PRIMARY MALIGNANT GLIOMA. J Neurosurg 1995,82(2):A350-A350.Google Scholar
- Zamorano L, Li QH, Tekyi-Mensah S, Gaspar L, Fontanesi J, Levin K: Permanent iodine-125 interstitial radiation therapy in the treatment of non-glioblastoma multiforme high-grade gliomas. Stereotactic and Functional Neurosurgery 2003,81(1-4):10-17. 10.1159/000075098PubMedGoogle Scholar
- Hitchon PW, Vangilder JC, Wen BC, Jani S, Wetjen B, Sawin PD: Brachytherapy in malignant glioma. Stereotactic and Functional Neurosurgery 1994,63(1-4):286-287.Google Scholar
- Ryken TC, Hitchon PW, Vangilder JC, Wen BC, Jani S: Interstitial brachytherapy versus cytoreductive surgery in recurrent malignant glioma. Stereotactic and Functional Neurosurgery 1994,63(1-4):241-245. 10.1159/000100320PubMedGoogle Scholar
- Malkin MG, Arbit E, Fass DE, Anderson LL, Osian A, Rosenblum MK, Shapiro JR, Leibel SA, Shapiro WR: STEREOTAXIC IMPLANTATION OF REMOVABLE HIGH-ACTIVITY IODINE-125 SOURCES FOR THE TREATMENT OF MALIGNANT GLIOMA. Neurology 1989,39(3 SUPPL. 1):263.Google Scholar
- Halligan JB, Stelzer KJ, Rostomily RC, Spence AM, Griffin TW, Berger MS: Operation and permanent low activity I-125 brachytherapy for recurrent high-grade astrocytomas. International Journal of Radiation Oncology Biology Physics 1996,35(3):541-547. 10.1016/S0360-3016(96)80017-4Google Scholar
- Wick W, Hartmann C, Engel C, Stoffels M, Felsberg J, Stockhammer F, Sabel MC, Koeppen S, Ketter R, Meyermann R, et al.: NOA-04 randomized phase III trial of sequential radiochemotherapy of anaplastic glioma with procarbazine, lomustine, and vincristine or temozolomide. J Clin Oncol 2009,27(35):5874-5880. 10.1200/JCO.2009.23.6497PubMedGoogle Scholar
- Chen AM, Chang S, Pouliot J, Sneed PK, Prados MD, Lamborn KR, Malec MK, McDermott MW, Berger MS, Larson DA: Phase I trial of gross total resection, permanent iodine-125 brachytherapy, and hyperfractionated radiotherapy for newly diagnosed glioblastoma multiforme. International Journal of Radiation Oncology Biology Physics 2007, 69: 825-830. 10.1016/j.ijrobp.2007.03.061Google Scholar
- Darakchiev BJ, Albright RE, Breneman JC, Warnick RE: Safety and efficacy of permanent iodine-125 seed implants and carmustine wafers in patients with recurrent glioblastoma multiforme. J Neurosurg 2008,108(2):236-242. 10.3171/JNS/2008/108/2/0236PubMedGoogle Scholar
- Keole S, Martinez J, Levin KJ, Frazier AJ, Zamorano L, Sloan A, Forman JD, Fontanesi JN: Survival analysis of patients with Glioblastoma multiforme treated with external radiotherapy followed by gamma knife radiosurgery or permanent Iodine-125 implant boost. International Journal of Radiation Oncology Biology Physics 2001,51(3 Supplement 1):256.Google Scholar
- Larson DA, Suplica JM, Chang SM, Lamborn KR, McDermott MW, Sneed PK, Prados MD, Wara WM, Nicholas MK, Berger MS: Permanent iodine 125 brachytherapy in patients with progressive or recurrent glioblastoma multiforme. Neuro-Oncology 2004,6(2):119-126. 10.1215/S1152851703000425PubMed CentralPubMedGoogle Scholar
- Loeffler JS, Alexander E, Wen PY, Shea WM, Coleman CN, Kooy HM, Fine HA, Nedzi LA, Silver B, Riese NE, et al.: RESULTS OF STEREOTAXIC BRACHYTHERAPY USED IN THE INITIAL MANAGEMENT OF PATIENTS WITH GLIOBLASTOMA. J Natl Cancer I 1990,82(24):1918-1921. 10.1093/jnci/82.24.1918Google Scholar
- Loeffler JS, Wen P, Alexander E III, Shea M, Black PM: RESULTS OF STEREOTACTIC INTERSTITIAL IRRADIATION USED IN TREATMENT OF RECURRENT GLIOBLASTOMA. Neurology 1991,41(3 SUPPL. 1):411.Google Scholar
- Sneed PK, Gutin PH, Larson DA, Malec MK, Phillips TL, Prados MD, Scharfen CO, Weaver KA, Wara WM: PATTERNS OF RECURRENCE OF GLIOBLASTOMA-MULTIFORME AFTER EXTERNAL IRRADIATION FOLLOWED BY IMPLANT BOOST. International Journal of Radiation Oncology Biology Physics 1994,29(4):719-727. 10.1016/0360-3016(94)90559-2Google Scholar
- Wen PY, Alexander E, Black PM, Fine HA, Riese N, Levin JM, Coleman CN, Loeffler JS: LONG-TERM RESULTS OF STEREOTAXIC BRACHYTHERAPY USED IN THE INITIAL TREATMENT OF PATIENTS WITH GLIOBLASTOMAS. Cancer 1994,73(12):3029-3036. 10.1002/1097-0142(19940615)73:12<3029::AID-CNCR2820731222>3.0.CO;2-4PubMedGoogle Scholar
- Chamberlain MC, Kormanik P: Concurrent carboplatin and iodine-125 brachytherapy for recurrent glioblastoma multiforme. Ann Neurol 1997,42(3):M152-M152.Google Scholar
- Koot RW, Maarouf M, Hulshof M, Voges J, Treuer H, Koedooder C, Sturm V, Bosch DA: Brachytherapy - Results of two different therapy strategies for patients with primary glioblastoma multiforme. Cancer 2000,88(12):2796-2802. 10.1002/1097-0142(20000615)88:12<2796::AID-CNCR19>3.0.CO;2-1PubMedGoogle Scholar
- Patel S, Breneman JC, Warnick RE, Albright RE, Tobler WD, van Loveren HR, Tew JM: Permanent iodine-125 interstitial implants for the treatment of recurrent glioblastoma multiforme. Neurosurgery 2000,46(5):1123-1128. 10.1097/00006123-200005000-00019PubMedGoogle Scholar
- Sneed PK, Prados MD, McDermott MW, Larson DA, Malec MK, Lamborn KR, Davis RL, Weaver KA, Wara WM, Phillips TL, et al.: LARGE EFFECT OF AGE ON THE SURVIVAL OF PATIENTS WITH GLIOBLASTOMA TREATED WITH RADIOTHERAPY AND BRACHYTHERAPY ROOST. Neurosurgery 1995,36(5):898-903. 10.1227/00006123-199505000-00002PubMedGoogle Scholar
- Suplica JM, Berger MS, McDermott MW, Chang SM, Prados MD, Sneed PK, Tsao MN, Wara WM, Larson DA: Total resection and permanent high-dose I-125 brachytherapy for recurrent or progressive glioblastoma. International Journal of Radiation Oncology Biology Physics 1999,45(3 SUPPL.):321.Google Scholar
- Heideman RL, Douglass EC, Krance RA, Fontanesi J, Langston JA, Sanford RA, Kovnar EH, Ochs J, Kuttesch J, Jenkins JJ, et al.: HIGH-DOSE CHEMOTHERAPY AND AUTOLOGOUS BONE-MARROW RESCUE FOLLOWED BY INTERSTITIAL AND EXTERNAL-BEAM RADIOTHERAPY IN NEWLY-DIAGNOSED PEDIATRIC MALIGNANT GLIOMAS. Journal of Clinical Oncology 1993,11(8):1458-1465.PubMedGoogle Scholar
- Kitchen ND, Hughes SW, Taub NA, Sofat A, Beaney RP, Thomas DGT: SURVIVAL FOLLOWING INTERSTITIAL BRACHYTHERAPY FOR RECURRENT MALIGNANT GLIOMA. J Neuro-Oncol 1994,18(1):33-39. 10.1007/BF01324601Google Scholar
- Sneed PK, Gutin PH, Prados MD, Phillips TL, Weaver KA, Wara WM, Larson DA: BRACHYTHERAPY OF BRAIN-TUMORS. Stereotactic and Functional Neurosurgery 1992,59(1-4):157-165. 10.1159/000098934PubMedGoogle Scholar
- Stupp R, Hegi ME, Mason WP, van den Bent MJ, Taphoorn MJB, Janzer RC, Ludwin SK, Allgeier A, Fisher B, Belanger K, et al.: Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol 2009,10(5):459-466. 10.1016/S1470-2045(09)70025-7PubMedGoogle Scholar
- Combs S, Debus J, Schulz-Ertner D: Radiotherapeutic alternatives for previously irradiated recurrent gliomas. BMC Cancer 2007, 7: 167. 10.1186/1471-2407-7-167PubMed CentralPubMedGoogle Scholar
- Chavantes MC, Zamorano L, Dujovny M, Milik G, Ausman JI: A NEW APPROACH FOR BRAIN METASTASES FROM LUNG CANCER IMAGE-GUIDED STEREOTAXIS AND IODINE-125 BRACHYTHERAPY. Chest 1988,94(1 SUPPL):85S.Google Scholar
- Ruge MI, Kocher M, Maarouf M, Hamisch C, Treuer H, Voges J, Sturm V: Comparison of Stereotactic Brachytherapy ((125)Iodine Seeds) with Stereotactic Radiosurgery (LINAC) for the Treatment of Singular Cerebral Metastases. Strahlentherapie Und Onkologie 2011,187(1):7-14. 10.1007/s00066-010-2168-4PubMedGoogle Scholar
- Ostertag CB, Kreth FW: INTERSTITIAL I-125 RADIOSURGERY FOR CEREBRAL METASTASES. British Journal of Neurosurgery 1995,9(5):593-603. 10.1080/02688699550040873PubMedGoogle Scholar
- Schulder M, Black PM, Shrieve DC, Alexander E, Loeffler JS: Permanent low-activity iodine-125 implants for cerebral metastases. J Neuro-Oncol 1997,33(3):213-221. 10.1023/A:1005798027813Google Scholar
- Alesch F, Hawliczek R, Koos WT: Interstitial irradiation of brain metastases. Acta Neurochirurgica Supplement; Stereotactic neuro-radio-surgery 1995, 29-34.Google Scholar
- Huang K, Sneed PK, Berger MS, Kunwar S, Larson DA, Wara WM, McDermott MW: Permanent iodine-125 brachytherapy for brain metastasis resection cavities. International Journal of Radiation Oncology Biology Physics 2002,54(2 Supplement):238.Google Scholar
- Ruge MI, Suchorska B, Maarouf M, Runge M, Treuer H, Voges J, Sturm V: Stereotactic (125)Iodine Brachytherapy for the Treatment of Singular Brain Metastases: Closing a Gap? Neurosurgery 2011,68(5):1209-1218.PubMedGoogle Scholar
- Dagnew E, Kanski J, McDermott MW, Sneed PK, McPherson C, Breneman JC, Warnick RE: Management of newly diagnosed single brain metastasis using resection and permanent iodine-125 seeds without initial whole-brain radiotherapy: a two institution experience. Neurosurg Focus 2007,22(3):E3.PubMedGoogle Scholar
- Huang K, Sneed PK, Kunwar S, Kragten A, Larson DA, Berger MS, Chan A, Pouliot J, McDermott MW: Surgical resection and permanent iodine-125 brachytherapy for brain metastases. J Neuro-Oncol 2009,91(1):83-93. 10.1007/s11060-008-9686-2Google Scholar
- Petr MJ, McPherson CM, Breneman JC, Warnick RE: Management of newly diagnosed single brain metastasis with surgical resection and permanent I-125 seeds without upfront whole brain radiotherapy. J Neuro-Oncol 2009,92(3):393-400. 10.1007/s11060-009-9868-6Google Scholar
- Prados M, Leibel S, Barnett CM, Gutin P: INTERSTITIAL BRACHYTHERAPY FOR METASTATIC BRAIN-TUMORS. Cancer 1989,63(4):657-660. 10.1002/1097-0142(19890215)63:4<657::AID-CNCR2820630410>3.0.CO;2-QPubMedGoogle Scholar
- Yakar D, Zamorano L, Dujovny M, Cooper M, Grandhe R, Martin F, Sheehan M: INTERSTITIAL TEMPORARY IMPLANTATION OF HIGH ACTIVITY IODINE-125 SOURCES FOR MALIGNANT GLIOMA AND BRAIN METASTASES. International Journal of Radiation Oncology, Biology, Physics 1989,17(SUPPL. 1):228.Google Scholar
- Zamorano L, Yakar D, Dujovny M, Sheehan M, Kim J: PERMANENT I-125 IMPLANT AND EXTERNAL BEAM RADIATION-THERAPY FOR THE TREATMENT OF MALIGNANT BRAIN-TUMORS. Stereotactic and Functional Neurosurgery 1992,59(1-4):183-192. 10.1159/000098940PubMedGoogle Scholar
- Zamorano L, Yakar D, Dujovny M, Sheehan M, Kim JH: Interstitial temporary implantation of high-activity iodine-125 sources for malignant glioma and brain metastases. Stereotactic and Functional Neurosurgery 1992,59(1-4):182.Google Scholar
- Kreth FW, Warnke PC, Ostertag CB: STEREOTAXIC INTERSTITIAL RADIOSURGERY AND PERCUTANEOUS RADIOTHERAPY FOR TREATMENT OF CEREBRAL METASTASES. Nervenarzt 1993,64(2):108-113.PubMedGoogle Scholar
- Ruge MI, Kickingereder P, Grau S, Hoevels M, Treuer H, Sturm V: Stereotactic biopsy combined with stereotactic (125)iodine brachytherapy for diagnosis and treatment of locally recurrent single brain metastases. J Neurooncol 2011,105(1):109-118. 10.1007/s11060-011-0571-zPubMedGoogle Scholar
- Barlas O, Bayindir C, Imer M, Ayan I, Darendeliler E: Non-resective management of pineoblastoma. Minimally Invasive Neurosurgery 2000,43(3):163-170. 10.1055/s-2000-14509PubMedGoogle Scholar
- Maarouf M, El Majdoub F, Buhrle C, Voges J, Lehrke R, Kocher M, Hunsche S, Treuer H, Sturm V: Pineal Parenchymal Tumors Management with Interstitial Iodine-125 Radiosurgery. Strahlentherapie Und Onkologie 2010,186(3):127-134. 10.1007/s00066-010-2096-3PubMedGoogle Scholar
- Kumar PP, Patil AA, Leibrock LG, Chu WK, Syh HW, McCaul GF, Reeves MA: CONTINUOUS LOW-DOSE RATE BRACHYTHERAPY WITH HIGH-ACTIVITY I-125 SEEDS IN THE MANAGEMENT OF MENINGIOMAS. International Journal of Radiation Oncology Biology Physics 1993,25(2):325-328. 10.1016/0360-3016(93)90355-YGoogle Scholar
- Kumar PP, Patil AA, Leibrock LG, Chu WK, Syh J, McCaul GF, Reeves MA: BRACHYTHERAPY - A VIABLE ALTERNATIVE IN THE MANAGEMENT OF BASAL MENINGIOMAS. Neurosurgery 1991,29(5):676-680. 10.1227/00006123-199111000-00006PubMedGoogle Scholar
- Kumar PP, Patil AA, Syh HW, Chu WK, Reeves MA: ROLE OF BRACHYTHERAPY IN THE MANAGEMENT OF THE SKULL BASE MENINGIOMA - TREATMENT OF SKULL BASE MENINGIOMAS. Cancer 1993,71(11):3726-3731. 10.1002/1097-0142(19930601)71:11<3726::AID-CNCR2820711141>3.0.CO;2-HPubMedGoogle Scholar
- Obasi PC, Barnett GH, Suh JH: Brachytherapy for intracranial meningioma using a permanently implanted iodine-125 seed. Stereotactic and Functional Neurosurgery 2002,79(1):33-43. 10.1159/000069502PubMedGoogle Scholar
- Patil AA, Kumar P, Leibrock LG: Response of extra-axial tumors to stereotactically implanted high-activity I-125 seeds. Stereotactic and Functional Neurosurgery 1995,64(3):139-152.PubMedGoogle Scholar
- Vuorinen V, Heikkonen J, Brander A, Setala K, Sane T, Randell T, Paetau A, Pohjola J, Mantyla M, Jaaskelainen J: Interstitial radiotherapy of 25 parasellar/clival meningiomas and 19 meningiomas in the elderly - Analysis of short-term tolerance and responses. Acta Neurochir 1996,138(5):495-508. 10.1007/BF01411167PubMedGoogle Scholar
- Kumar PP, Good RR, Cox TA, Leibrock LG, Skultety FM: REVERSAL OF VISUAL IMPAIRMENT AFTER INTERSTITIAL IRRADIATION OF PITUITARY-TUMOR. Neurosurgery 1986,18(1):82-84. 10.1227/00006123-198601000-00014PubMedGoogle Scholar
- Kumar PP, Good RR, Skultety FM, Leibrock LG, Severson GS: RADIATION-INDUCED NEOPLASMS OF THE BRAIN. Cancer 1987,59(7):1274-1282. 10.1002/1097-0142(19870401)59:7<1274::AID-CNCR2820590708>3.0.CO;2-HPubMedGoogle Scholar
- Kumar PP, Good RR, Skultety FM, Leibrock LG: LOCAL-CONTROL OF RECURRENT CLIVAL AND SACRAL CHORDOMA AFTER INTERSTITIAL IRRADIATION WITH I-125 - NEW TECHNIQUES FOR TREATMENT OF RECURRENT OR UNRESECTABLE CHORDOMAS. Neurosurgery 1988,22(3):479-483. 10.1227/00006123-198803000-00005PubMedGoogle Scholar
- Kumar PP: HIGH ACTIVITY IODINE-125 ENDOCURIETHERAPY FOR SKULL BASE TUMORS. International Journal of Radiation Oncology, Biology, Physics 1990,19(SUPPL. 1):226.Google Scholar
- Kumar PP, Good RR, Leibrock LG, Mawk JR, Yonkers AJ, Ogren FP: HIGH-ACTIVITY IODINE 125 ENDOCURIETHERAPY FOR RECURRENT SKULL BASE TUMORS. Cancer 1988,61(8):1518-1527. 10.1002/1097-0142(19880415)61:8<1518::AID-CNCR2820610807>3.0.CO;2-DPubMedGoogle Scholar
- Collins SP, Coppa ND, Zhang Y, Collins BT, McRae DA, Jean WC: CyberKnife (R) radiosurgery in the treatment of complex skull base tumors: analysis of treatment planning parameters. Radiation Oncology 2006., 1:Google Scholar
- Minniti G, Amichetti M, Enrici RM: Radiotherapy and radiosurgery for benign skull base meningiomas. Radiat Oncol 2009, 4: 42. 10.1186/1748-717X-4-42PubMed CentralPubMedGoogle Scholar
- El Majdoub F, Brunn A, Berthold F, Sturm V, Maarouf M: Stereotaktische interstitielle Radiochirurgie zur Behandlung des intrakraniellen Rosai-Dorfman-Syndroms. Ein neuer therapeutischer Ansatz. Strahlentherapie Und Onkologie 2009,185(2):109-112. 10.1007/s00066-009-1911-1PubMedGoogle Scholar
- Suarez JC, Viano JC, Zunino S, Herrera EJ, Gomez J, Tramunt B, Marengo I, Hiramatzu E, Miras M, Pena M, et al.: Management of child optic pathway gliomas: new therapeutical option. Childs Nervous System 2006,22(7):679-684. 10.1007/s00381-005-0021-3Google Scholar
- Barlas O, Bayindir C, Can M: Interstitial irradiation for craniopharyngioma. Acta Neurochir 2000,142(4):389-395. 10.1007/s007010050447PubMedGoogle Scholar
- Frank F, Fabrizi AP, Frank G, Fioravanti A: Stereotactic management of craniopharyngiomas. Stereotactic and Functional Neurosurgery 1995,65(1-4):176-183. 10.1159/000098691PubMedGoogle Scholar
- El Majdoub F, Simon T, Hoevels M, Berthold F, Sturm V, Maarouf M: Interstitial Brachytherapy using Stereotactic Implanted 125Iodine Seeds for Recurrent Medulloblastoma. Clinical Oncology, in press. Corrected ProofGoogle Scholar
- Chalifoux R, Elisevich K: Effect of ionizing radiation on partial seizures attributable to malignant cerebral tumors. Stereotactic and Functional Neurosurgery 1996,67(3-4):169-182.PubMedGoogle Scholar
- Chamberlain MC, Barba D, Kormanik P, Berson AM, Saunders WM, Shea MC: CONCURRENT CISPLATIN THERAPY AND IODINE-125 BRACHYTHERAPY FOR RECURRENT MALIGNANT BRAIN-TUMORS. Archives of Neurology 1995,52(2):162-167. 10.1001/archneur.1995.00540260066018PubMedGoogle Scholar
- Tacke U, Karger D, Spreer J, Berlis A, Nikkhah G, Korinthenberg R: Incidence of vasculopathy in children with hypothalamic/chiasmatic gliomas treated with brachytherapy. Childs Nervous System 2011,27(6):961-966. 10.1007/s00381-010-1370-0Google Scholar
- Bampoe J, Nag S, Leung P, Laperriere N, Bernstein M: Brain necrosis after permanent low-activity iodine-125 implants: case report and review of toxicity from focal radiation. Brain Tumor Pathol 2000,17(3):139-145. 10.1007/BF02484285PubMedGoogle Scholar
- Agbi CB, Bernstein M, Laperriere N, Leung P, Lumley M: PATTERNS OF RECURRENCE OF MALIGNANT ASTROCYTOMA FOLLOWING STEREOTAXIC INTERSTITIAL BRACHYTHERAPY WITH I-125 IMPLANTS. International Journal of Radiation Oncology Biology Physics 1992,23(2):321-326. 10.1016/0360-3016(92)90748-7Google Scholar
- Wara WM: RADIATION-THERAPY FOR BRAIN-TUMORS. Cancer 1985,55(9):2291-2295. 10.1002/1097-0142(19850501)55:9+<2291::AID-CNCR2820551437>3.0.CO;2-CPubMedGoogle Scholar
- Tihan T, Barletta J, Parney I, Lamborn K, Sneed PK, Chang S: Prognostic value of detecting recurrent glioblastoma multiforme in surgical specimens from patients after radiotherapy: should pathology evaluation atter treatment decisions? Human Pathology 2006,37(3):272-282. 10.1016/j.humpath.2005.11.010PubMedGoogle Scholar
- Frank F, Gaist G, Piazza G, Ricci RF, Sturiale C, Galassi E: STEREOTAXIC BIOPSY AND RADIOACTIVE IMPLANTATION FOR INTERSTITIAL THERAPY OF TUMORS OF THE PINEAL REGION. Surgical Neurology 1985,23(3):275-280. 10.1016/0090-3019(85)90095-3PubMedGoogle Scholar
- Houston SC, Crocker IR, Brat DJ, Olson JJ: Extraneural metastatic glioblastoma after interstitial brachytherapy. International Journal of Radiation Oncology Biology Physics 2000,48(3):831-836. 10.1016/S0360-3016(00)00662-3Google Scholar
- Correa CF, Teixeira MJ, Rogano LA, Oliveira S, Miziara M, Gusmao C, Bouza AA: 125 I brachytherapy for treatment of CNS tumors. Stereotactic and Functional Neurosurgery 1996,67(1-2):93.Google Scholar
- Leibel SA, Gutin PH, Phillips TL, Wara WM, Weaver KA, Lamb S: INTERSTITIAL IMPLANTATION OF HIGH-ACTIVITY IODINE-125 SOURCES FOR THE TREATMENT OF RECURRENT MALIGNANT BRAIN TUMORS. International Journal of Radiation Oncology, Biology, Physics 1984,10(SUPPL. 2):144-145.Google Scholar
- Leibel SA, Gutin PH, Phillips TL, Wara WM, Weaver KA, Lamb S: INTERSTITIAL BRACHYTHERAPY WITH REMOVABLE HIGH-ACTIVITY I-125 SOURCES FOR RECURRENT MALIGNANT BRAIN-TUMORS. American Journal of Clinical Oncology-Cancer Clinical Trials 1985,8(1):20-20.Google Scholar
- Vordermark D: Brachytherapy - Results of two different therapy strategies for patients with primary glioblastoma multiforme. Cancer 2001,91(6):1185-1186. 10.1002/1097-0142(20010315)91:6<1185::AID-CNCR1116>3.0.CO;2-QPubMedGoogle Scholar
- Rostomily RC, Halligan J, Geyer R, Stelzer K, Lindsley K, Berger MS: Permanent low-activity I-125 seed placement for the treatment of pediatric brain tumors: Preliminary experience. Pediatric Neurosurgery 2001,34(4):198-205. 10.1159/000056020PubMedGoogle Scholar
- Korinthenberg RND, Trippel M, Ostertag C, Nikkhah G: Long-Term Results of Brachytherapy with temporary iodine-125 Seeds in Children with low-grade gliomas. International Journal Radiation Oncology Biology Physics 2011,79(4):1131-1138. 10.1016/j.ijrobp.2009.12.040Google Scholar
- Ruge MI, Simon T, Suchorska B, Lehrke R, Hamisch C, Koerber F, Maarouf M, Treuer H, Berthold F, Sturm V, et al.: Stereotactic brachytherapy with iodine-125 seeds for the treatment of inoperable low-grade gliomas in children: long-term outcome. J Clin Oncol 2011,29(31):4151-4159. 10.1200/JCO.2011.37.3381PubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.