- Open Access
Linac-based stereotactic radiotherapy and radiosurgery in patients with meningioma
© Kaul et al.; licensee BioMed Central Ltd. 2014
- Received: 9 December 2013
- Accepted: 16 March 2014
- Published: 20 March 2014
It was our purpose to analyze long-term clinical outcome and to identify prognostic factors after Linac-based fractionated stereotactic radiotherapy (Linac-based FSRT) and stereotactic radiosurgery (SRS) in patients with intracranial meningiomas.
Materials and methods
Between 10/1995 and 03/2009, 297 patients with a median age of 59 years were treated with FSRT for intracranial meningioma. 50 patients had a Grade I meningioma, 20 patients had a Grade II meningioma, 12 patients suffered from a Grade III tumor, and in 215 cases no histology was obtained (Grade 0). Of the 297 patients, 144 underwent FSRT as their primary treatment and 158 underwent postoperative FSRT. 179 patients received normofractionated radiotherapy (nFSRT), 92 patients received hypofractionated FSRT (hFSRT) and 26 patients underwent SRS. Patients with nFSRT received a mean total dose of 57.31 ± 5.82 Gy, patients with hFSRT received a mean total dose of 37.6 ± 4.4 Gy and patients who underwent SRS received a mean total dose of 17.31 ± 2.58 Gy.
Median follow-up was 35 months. Overall progression free survival (PFS) was 92.3% at 3 years, 87% at 5 years and 84.1% at 10 years. Patients with adjuvant radiotherapy showed significantly better PFS-rates than patients who had been treated with primary radiotherapy. There was no significant difference between PFS-rates of nFSRT, hFSRT and SRS patients. PFS-rates were independent of tumor size. Patients who had received nFSRT showed less acute toxicity than those who had received hFSRT. In the Grade 0/I group the rate of radiologic focal reactions was significantly lower than in the atypical/malignant histology group.
This large study showed that FSRT is an effective and safe treatment modality with high PFS-rates for intracranial meningioma. We identified “pathological grading” and and “prior surgery” as significant prognostic factors.
- Local control
- Stereotactic fractionated radiotherapy
- Image-guided radiotherapy
Meningioma is the second most common primary intracranial tumor that arises from the cap cells of the arachnoid membrane and is more common in women than in men, incidence peaks in the fifth, sixth, and seventh decade. About 85% of meningiomas are slow growing Grade I tumors, approximately 10% are Grade II atypical lesions, and 3–5% are anaplastic Grade III lesions.
Microsurgical resection is usually the treatment of choice for symptomatic tumors but may not always be possible, due to proximity to critical structures. Higher Grade tumors have higher risks of recurrence after surgical resection[2, 3]. Postoperative FSRT may prolong time to recurrence and is usually recommended after incomplete resection. Inoperable symptomatic Grade I meningiomas can be treated using FSRT with results comparable to those of complete resection[4, 5].
Grade II meningiomas are found in 5-20% of the patients; 40-60% of these patients remain disease-free at 10 years after definitive treatment[6, 7]. Grade III tumors account for 1-5% and recurrence-free survival is usually less than 2 years. Grade II/III meningiomas are commonly treated with postoperative FSRT after incomplete or complete resection[8, 9]. In the present study, we analyzed the results in one of the largest populations of meningioma-patients treated with Linac-based image-guided FSRT in a single institution. The purpose was to gain information on long-term clinical outcome, relevant prognostic factors and contribute to the ongoing multidisciplinary discussions.
Treatment decisions, patient selection and dose regimens
We performed a retrospective analysis of 372 patients who underwent FSRT of an intracranial meningioma between 10/1995 and 03/2009. 5 patients receiving re-irradiation due to a secondary meningioma were excluded. In 3 patients the diagnosis was questionable, 62 patients were excluded because of incomplete follow-up. In 5 patients the fractionation scheme was not determinable. Follow-up data were analyzed until March 2010. The study was approved by the local Ethics Committée of Charité University Medicine, Berlin. The research was in compliance with the Helsinki Declaration.
In our institution treatment decisions are based on an interdisciplinary vote. Adjuvant FSRT is offered to all resected Grade II and III meningioma-patients; Symptomatic Grade I meningiomas are treated with adjuvant RT only after incomplete resection or when recurrence occurs after total resection. Inoperable Grade II or III tumors as well as inoperable symptomatic Grade I tumors are treated using primary FSRT.
1.6-2.2 Gy were considered normofractionated (nFSRT), 2.2-5 Gy were considered hypofractionated (hFSRT) and high single doses delivered in less than 5 sessions were considered stereotactic radiosurgery (SRS).
Tumors in close proximity to critical structures were assigned to nFSRT, while large tumors (> 2 cm) distant to critical structures underwent hFSRT and small tumors (< 2 cm) were treated by SRS.
Stratification and variables
Patient data were analyzed according to grading, location, predicted peri-operative risk/operability, tumor size and sequence of therapy. Two groups were defined: group 1 encompasses all Grade I meningiomas, as well as all meningiomas with no histology available (Grade 0). Group 2 encompasses all Grade II and III meningiomas.
The tumor location was divided into 3 groups according to the Novel “CLASS” Algorithmic Scale for Patient Selection in Meningioma Surgery: low risk, medium risk, high risk and optical nerve sheath (ONSM).
Follow-up examinations, including MRI as well as clinical, and neurologic examinations were performed at 6 weeks, 3 months, 9 months, 15 months after treatment and then annually.
We distinguished between primary radiation treatment and postoperative radiotherapy. Acute toxicity in the first 90 days after FSRT was graded using a modified version of the Common Terminology Criteria of Adverse Events (CTCAE v4.0).
From 1995–2003 meningioma patients underwent “sharp” fixation using a stereotactic head ring and an oral bite Plate. A 6 MV Linac (Varian® USA) with an add-on micro-multileaf collimator (mMLC) (BrainLab® Co, Germany) was used. Coordinats for SRS were set by a laser-based stereotactic localizer. This set up allowed delivering shaped beams. In 2004 we started using Novalis® (BrainLab®) with beam shaping capability using build-in MLC and image guidance. Novalis ExacTrac® image guided frameless system enabled us to image the patient at any couch position using a frameless positioning array. MRI/CT-fusion planning was performed. The three-dimensional treatment planning system Brainscan® (Brain Lab AG, Germany) was used, which was later replaced by iplanRT®. The gross tumor volume (GTV) was defined as the area of contrast enhancement on T1-weighted MRI images, the planning target volume (PTV) included a 2 mm isotropic safety margin. The dose was prescribed to a reference point, which was the isocenter (or the center of GTV), though 100% was not the maximum dose but the dose at the aforementioned reference point. Patients received the prescribed dose to the 80th isodose at the tumor margin plus a safety margin of 5 mm in Grade II and III meningiomas. Organs at risk (OAR) such as optic nerves, the chiasm, lenses and the brainstem, were delineated. Dose constraints were according to the data published by Emami et al. 1991. The TD 5/5 to be respected was as follows: for optic nerves 50 Gy, for chiasm 50 Gy, for lenses 10 Gy and for the brainstem 50 Gy, respectively.
Formulas and statistics
The equivalent 2 Gy dose (EQD2) was calculated according to the formula,EQD2 = n × d × (a/b + d)/(a/b + 2).
All statistical analyses were performed using IBM SPSS Statistics 19 (New York, USA).
Characteristics of the 297 meningioma patients analyzed
(n = 297)
(n = 265)
(n = 32)
Age with beginn of RT
Mean total dose
Follow up-time in months
Tumors were grouped according to the “CLASS” Algorithmic Scale for Patient Selection in Meningioma Surgery: 9.8% had a low risk localization, 13.5% showed a moderate risk localization, 71.7 showed s high risk localization and 5.1 percent were ONSM.
Progression free survival
Group 1 (unknown/Grade I)
Group 2 (Grade II/III)
Volume < 60 ccm
Volume > 60 ccm
Tumor response rates
The most common acute Grade I symptoms for the entire cohort were headache, fatigue, local alopecia and local skin reaction. The most common acute Grade II symptoms were headache, vertigo and nausea.
The difference in acute toxicity between group 1 and group 2 was not significant.
Patients with tumors smaller than 60 cm3 did not show a significantly different rate of acute toxicity than patients with a tumor diameter above 60 cm3 (n = 192, p = 0.28). As mentioned above though there is a bias in treatment , since smaller tumor usually received SRS.
There was a significant difference in acute toxicity for different fraction schemes: Patients receiving nFSRT showed more acute toxicity compared to hFSRT or SRS (67.1% vs. 47.9% and 35%). This difference was mainly due to Grade I reactions (FSRT: 50.3%, hFSRT: 31% SRS: 10%; p < 0.001), Grade II and III reactions were even a bit higher in Patients receiving hFSRT or SRS, although this effect was not significant.
For n = 276 patients (92.9%) of the entire cohort evaluation of late toxicity was available, 98 (35.5%) showed late toxicity. The most common Grade I symptoms were headache and fatigue. The most common Grade II symptoms were headache, dizziness and seizures. Grade III late toxicity was seen 0.7% of the patients.
The difference in late toxicity between group 1 and group 2 was not significant.
Focal reactions and corticosteroid treatment
New peritumoral edema during follow-up was described in 14.8% of all patients in the entire cohort. In group 1 the rate of focal reaction was significantly lower than in group 2; 12.8% compared to 31.2% (p = 0.014).
Therapy with corticosteroids was necessary in 12.8% of the patients. There was no significant difference between group 1 and group 2 concerning treatment with steroids (16.2% vs. 13.3%).
This study is the second largest analysis of Linac-based FSRT for intracranial Grade I-III meningiomas after the study by Milker-Zabel et al.. We show here that Linac-based FSRT is a safe option in the treatment of intracranial meningiomas with a low risk of acute or late toxicity and can thus corroborate the findings by Milker-Zabel et al. Patients with meningiomas that score high on the “CLASS” -scale are more likely to receive primary radiotherapy meaning that the patients have undergone negative preselection. Considering this fact the good PFS rates seen after radiotherapy are even more encouraging.
In the entire cohort (Grade 0-III) progression free survival was 92.3% at 3 years, 87% at 5 years and 84.1% at 10 years. Similar results have been shown for gamma knife radiosurgery of Grade I-III meningiomas by Nakaya et al. who found PFS-rates of 94%, 83%, and 58% at 3, 5 and 10 years respectively.
In the benign/unknown histology group PFS-rates were 96.8%, 92.7% and 89.6% at 3, 5 and 10 years. In a study by Compten et al. similar PFS-rates for FSRT-treated benign and unknown histology meningiomas are shown: 96.3% at 3 years and 93% at 5 years.
Only looking at patients with histologically proven Grade I meningioma PFS-rates were 93.9% at 3 years and 85.8% at 5 years and at 10 years. Milker-Zabel et al. found similar PFS-rates of 98.5% at 3 years, 90.5% at 5 years, and 89% at 10 years for FSRT-treated Grade I meningiomas. In a study by Debus et al. the overall actuarial survival rate of patients with WHO Grade I meningioma was 97% at 5 years and 96% at 10 years. Kreil et al. showed similar results for benign histology meningiomas treated with gamma knife radiosurgery: 98.5% at 5 years and 97.2% at 10 years.
We found that group 2 had PFS-rates 52.6% at 3 years and 19.7% at 5 years, 10 year rates could not be calculated since all cases had been censored. Compten et al. showed a slightly lower PFS-rate of 40% for GradeII/III meningiomas at 3 years.
Patients with Grade II meningioma had PFS-rates of 62.7% at 3 years and 41.8% at 5 years, 10 year rates could not be calculated since all cases had been censored. Milker-Zabel et al. showed better recurrence-free survival rates of 96% at 3 years, 89% at 5 years, and 67% at 10 years for Grade II meningiomas. However these data might might be a statistically biased due to the small number of patients with proven Grade II meningioma.
In general it must be mentioned that the role of adjuvant radiotherapy of Grade II/III meningiomas remains unclear due to inconsistent evidence from retrospective studies.
Independent of histology we showed 5 year PFS-rates of 96.8% for patients who had undergone primary radiation and 78.1% for patients who had received surgical resection. Nutting et al. found a 5-year PFS-rate of 92% in patients with benign meningiomas which had been treated with adjuvant conventional FSRT after surgery. In a study by Goldsmith et al. a 5-year progression-free survival rate of 89% was reported for patients with subtotally resected Grade I meningioma after postoperative FSRT.
We found a significant difference in PFS-rates for patients who had undergone surgical resection and those who had received primary radiation (p < 0.001, log-rank test). This result was to be expected since Grade I meningiomas are usually not treated with adjuvant FSRT after complete resection.
Milker-Zabel et al. found that patients with a tumor volume >60 cm3 had a higher recurrence rate than patients with a lower tumor volume. We did not find significant differences in PFS-rates between these two groups. However, considering that only 11 of the entire cohort showed a tumor volume above 60 cm3, the number of cases analyzed here might just be to low to be significant.
We found that patients with nFSRT showed more acute toxicity than those with hFSRT or SRS. This difference was mainly due to Grade I reactions. The rate of Grade II and III reactions was higher in patients who received hFSRT or SRS (however this effect was not significant). This might be due to the prolonged treatment in nFSRT-patients. These patients had the time to develop Grade I reactions whereas hypofractionated patients might have skipped Grade I reactions and developed Grade II/III reactions faster.
In the entire cohort 35.5% of the patients showed late toxicity. Compten et al. found late toxicity in 20.8% of meningioma patients after FSRT. Hamm et al. found late toxicity of only 14.3% in a cohort of 224 patients (183 nFSRT, 30 hFSRT and 11 SRS). However it has to be noticed that retrospective analyses of toxicity are bias-prone due to interobserver variabilities. Also the relatively high total dose delivered may play a role here.
Engenhart et al. who found 30% of patients to show chronic late toxicity after a mean single fraction dose of 29 Gy which is similar to 36% late toxicity found in SRS patients in this study.
We found Grade III late toxicity in 0.7% of the patients, which is similar to the results shown in a study by Goldsmith et al. where 3.6% of 140 patients treated with a radiation dose of 57.6 Gy showed Grade III late toxicity. Jalali et al. found chronic late toxicity in 6% of 67 patients.
In our study new peritumoral edema was described in 14.8% of all patients in the entire cohort, slightly worse results were found in a study by Chang et al., where radiologic complications were seen in 23.6% of 179 patients treated with gamma knife radiosurgery after a mean follow-up of 37.3 months.
The good long-term clinical outcome of FSRT in regard to its high effectiveness and low morbidity is indicating that it should be considered as an equivalent treatment option complementary to microsurgery and gamma knife radiosurgery.
- van Alkemade H, de Leau M, Dieleman EM, Kardaun JW, van Os R, Vandertop WP, van Furth WR, Stalpers LJ: Impaired survival and long-term neurological problems in benign meningioma. Neuro Oncol 2012, 14: 658-666. 10.1093/neuonc/nos013PubMed CentralView ArticlePubMedGoogle Scholar
- Mirimanoff RO, Dosoretz DE, Linggood RM, Ojemann RG, Martuza RL: Meningioma: analysis of recurrence and progression following neurosurgical resection. J Neurosurg 1985, 62: 18-24. 10.3171/jns.1985.62.1.0018View ArticlePubMedGoogle Scholar
- Milker-Zabel S, Zabel-du Bois A, Huber P, Schlegel W, Debus J: Fractionated stereotactic radiation therapy in the management of benign cavernous sinus meningiomas : long-term experience and review of the literature. Strahlentherapie und Onkologie: Organ der Deutschen Rontgengesellschaft 2006, 182: 635-640. 10.1007/s00066-006-1548-2View ArticleGoogle Scholar
- Glaholm J, Bloom HJ, Crow JH: The role of radiotherapy in the management of intracranial meningiomas: the Royal Marsden Hospital experience with 186 patients. Int J Radiat Oncol Biol Phys 1990, 18: 755-761. 10.1016/0360-3016(90)90394-YView ArticlePubMedGoogle Scholar
- Thilmann C, Schulz-Ertner D, Unterberg A, Wannenmacher M, Debus J: Stereotaktische strahlenbehandlung schädelbasisnaher meningeome und schwannome. Dtsch Arztebl 2004, Heft 15: 1022-1026.Google Scholar
- Claus EB, Bondy ML, Schildkraut JM, Wiemels JL, Wrensch M, Black PM: Epidemiology of intracranial meningioma. Neurosurgery 2005, 57: 1088-1095. discussion 1088–1095 10.1227/01.NEU.0000188281.91351.B9View ArticlePubMedGoogle Scholar
- Gondi V, Tome WA, Mehta MP: Fractionated radiotherapy for intracranial meningiomas. J Neuro-Oncol 2010, 99: 349-356. 10.1007/s11060-010-0368-5View ArticleGoogle Scholar
- Engenhart-Cabillic R, Farhoud A, Sure U, Heinze S, Henzel M, Mennel HD, Bertalanffy H: Clinicopathologic features of aggressive meningioma emphasizing the role of radiotherapy in treatment. Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft 2006, 182: 641-646. 10.1007/s00066-006-1555-3View ArticleGoogle Scholar
- DeVries A, Munzenrider JE, Hedley-Whyte T, Hug EB: [The role of radiotherapy in the treatment of malignant meningiomas]. Strahlentherapie und Onkologie: Organ der Deutschen Rontgengesellschaft 1999, 175: 62-67. 10.1007/BF02753844View ArticleGoogle Scholar
- Lee JH, Sade B: The novel “CLASS” algorithmic scale for patient selection in meningioma surgery. In Meningiomas. Edited by: Lee JH. London: Springer London; 2009:217-221.View ArticleGoogle Scholar
- Emami B, Lyman J, Brown A, Coia L, Goitein M, Munzenrider JE, Shank B, Solin LJ, Wesson M: Tolerance of normal tissue to therapeutic irradiation. Int J Radiat Oncol Biol Phys 1991, 21: 109-122.View ArticlePubMedGoogle Scholar
- Milker-Zabel S, Zabel A, Schulz-Ertner D, Schlegel W, Wannenmacher M, Debus J: Fractionated stereotactic radiotherapy in patients with benign or atypical intracranial meningioma: long-term experience and prognostic factors. Int J Radiat Oncol Biol Phys 2005, 61: 809-816. 10.1016/j.ijrobp.2004.07.669View ArticlePubMedGoogle Scholar
- Maire JP, Vendrely V, Dautheribes M, Bonichon N, Darrouzet V: [Fractionated radiotherapy of intracranial meningiomas and neurinomas]. Cancer Radiotherapie: journal de la Societe francaise de radiotherapie oncologique 2000, 4 Suppl 1: 84s-94s.Google Scholar
- Nakaya K, Chernov M, Kasuya H, Izawa M, Hayashi M, Kato K, Kubo O, Muragaki Y, Iseki H, Hori T: Risk factors for regrowth of intracranial meningiomas after gamma knife radiosurgery: importance of the histopathological grade and MIB-1 index. Minim Invasive Neurosurg 2009, 52: 216-221. 10.1055/s-0029-1243244View ArticlePubMedGoogle Scholar
- Compter I, Zaugg K, Houben RM, Dings JT, Bosmans G, Buescher C, Anten MM, Baumert BG: High symptom improvement and local tumor control using stereotactic radiotherapy when given early after diagnosis of meningioma. A multicentre study. Strahlentherapie und Onkologie: Organ der Deutschen Rontgengesellschaft 2012, 188: 887-893. 10.1007/s00066-012-0155-7View ArticleGoogle Scholar
- Debus J, Wuendrich M, Pirzkall A, Hoess A, Schlegel W, Zuna I, Engenhart-Cabillic R, Wannenmacher M: High efficacy of fractionated stereotactic radiotherapy of large base-of-skull meningiomas: long-term results. J Clin Oncol: J Am Soc Clin Oncol 2001, 19: 3547-3553.Google Scholar
- Kreil W, Luggin J, Fuchs I, Weigl V, Eustacchio S, Papaefthymiou G: Long term experience of gamma knife radiosurgery for benign skull base meningiomas. J Neurol Neurosurg Psychiatry 2005, 76: 1425-1430. 10.1136/jnnp.2004.049213PubMed CentralView ArticlePubMedGoogle Scholar
- Stessin AM, Schwartz A, Judanin G, Pannullo SC, Boockvar JA, Schwartz TH, Stieg PE, Wernicke AG: Does adjuvant external-beam radiotherapy improve outcomes for nonbenign meningiomas? a surveillance, epidemiology, and end results (SEER)-based analysis. J Neurosurg 2012, 117: 669-675. 10.3171/2012.7.JNS111439View ArticlePubMedGoogle Scholar
- Nutting C, Brada M, Brazil L, Sibtain A, Saran F, Westbury C, Moore A, Thomas DG, Traish D, Ashley S: Radiotherapy in the treatment of benign meningioma of the skull base. J Neurosurg 1999, 90: 823-827. 10.3171/jns.1999.90.5.0823View ArticlePubMedGoogle Scholar
- Goldsmith BJ, Wara WM, Wilson CB, Larson DA: Postoperative irradiation for subtotally resected meningiomas. A retrospective analysis of 140 patients treated from 1967 to 1990. J Neurosurg 1994, 80: 195-201. 10.3171/jns.1994.80.2.0195View ArticlePubMedGoogle Scholar
- Engenhart R, Kimmig BN, Hover KH, Wowra B, Sturm V, van Kaick G, Wannenmacher M: Stereotactic single high dose radiation therapy of benign intracranial meningiomas. Int J Radiat Oncol Biol Phys 1990, 19: 1021-1026. 10.1016/0360-3016(90)90028-IView ArticlePubMedGoogle Scholar
- Jalali R, Loughrey C, Baumert B, Perks J, Warrington AP, Traish D, Ashley S, Brada M: High precision focused irradiation in the form of fractionated stereotactic conformal radiotherapy (SCRT) for benign meningiomas predominantly in the skull base location. Clin Oncol (R Coll Radiol) 2002, 14: 103-109. 10.1053/clon.2001.0040View ArticleGoogle Scholar
- Chang JH, Chang JW, Choi JY, Park YG, Chung SS: Complications after gamma knife radiosurgery for benign meningiomas. J Neurol Neurosurg Psychiatry 2003, 74: 226-230. 10.1136/jnnp.74.2.226PubMed CentralView ArticlePubMedGoogle Scholar
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