Iodine-125 seed brachytherapy for early stage prostate cancer: a single-institution review
© Zuber et al.; licensee BioMed Central. 2015
Received: 29 September 2014
Accepted: 2 February 2015
Published: 22 February 2015
We are reporting the five-year biochemical control, toxicity profile and dosimetric parameters using iodine-125 low dose rate brachytherapy (BT) as monotherapy for early stage prostate cancer at a single institution.
Material and methods
Between April 2006 and December 2010, 169 men with early stage prostate cancer were treated with BT. Biochemical failure was defined using the Phoenix definition (nadir + 2 ng/mL). Treatment-related morbidities, including urinary, rectal and sexual function, were measured, applying the International Prostate Symptom Score (IPSS), the 7-grade Quality of Life Scale (QoL) and medical status, the International Consultation on Incontinence Modular Questionnaire (ICIQ), the International Index of Erectile Function (IIEF-5) and the Common Terminology Criteria for Adverse Events (CTCAE v4.03). Seed migration and loss, dosimetric parameters and learning effects were also analyzed.
Medium follow-up time was 50 months (range, 1–85 months). The five-year biochemical failure rate was 7%. Acute proctitis rates were 19% (grade 1) and 1% (grade 2), respectively. The overall incidence of incontinence was 19% (mild), 16% (moderate) and < 1% (severe). An increase in IPSS ≥ 5 points was detected in 59% of patients, with 38% regaining their baseline. Seed dislocation was found in 24% of patients and correlated with D90 and V100. A learning curve was found for seed migration, D90 and V100. QoL correlated with the general health condition of patient, incontinence symptoms and IPSS.
BT for early stage prostate cancer offers excellent five-year biochemical control with low toxicities. QoL aspects are favorable. A learning curve was detected for procedural aspects but its impact on patient relevant endpoints remains inconclusive.
Prostate cancer is the most common malignancy in men in the developed world . In Germany, the annual incidence is estimated to be as high as 48,650 new cases, accounting for approximately 22% of all cancer in males .
Iodine-125 low dose rate brachytherapy (BT) is an effective modality to administer a high dose to the prostate while minimizing toxicities for the adjacent organs at risk . For selected patients with low and favorable intermediate-risk prostate cancer, BT is equally effective in controlling the disease as radical prostatectomy . For men who place a premium on avoiding side effects of treatment and who accept the possible risk of late metastasis or death, also lack of treatment with an active surveillance strategy can be appropriate .
Judging the quality of an implant by dosimetric parameters is recommended by the American Brachytherapy Society (ABS)  and the European Society for Radiotherapy & Oncology, European Association of Urology and European Organization for Research and Treatment of Cancer (ESTRO/EAU/EORTC) . Dose homogeneity within the target volume is much more difficult to achieve during BT than during external beam radiotherapy (EBRT), and implants are rarely geometrically perfect. To avoid partial underdosage of the target volume, it may be necessary to accept hot spots in other parts of the target volumes, but it is not clear how much dose heterogeneity should be considered excessive .
A known phenomenon after BT is the detachment of seeds from their initial site and migration to other organs. Seed migration may be identified in up to 55 percent of patients who are monitored with routine chest x-rays . Also dislocation within the abdomen or pelvis is observed, with the majority of patients being asymptomatic . Only very few migration-related sequelae have been reported, such as cases of myocardial infarction and radiation pneumonitis [11,12].
It stands to reason that quality of life (QoL) can be influenced by the adverse effects of BT. Typically, these are expressed in the gastrointestinal and genitourinary tract system. Toxicities after BT that have been reported are challenging to compare due to differences in follow-up time, disease profile at presentation, study endpoints and treatment regimens, which differ from a permanent implant alone to the combination with EBRT and/or androgen ablation . According to the literature, urinary retention occurred in 5-22% of the patients after seed implantation alone [14,15]. Acute urinary symptoms increased by over 100% in patients treated either with BT alone or BT combined with EBRT. However, most studies found that about 90% of patients will have normalized their urinary complaints by one year postimplant [16,17]. Urinary incontinence after BT (without associated transurethral resection of the prostate) is reported in 0-19% of patients [18,19]. The incidence of radiation proctitis following implantation ranges from 1-19% in patients treated with implants alone [20,21]. Poor sexual function is reported in 43-48% of patients .
Several retrospective studies demonstrated the impact of implantation experience on the quality of the procedure: Lefur et al. , observed a learning curve to achieve consistent implantation parameters, which lead to a significant decrease in the dose to the rectum. They found no impact on the dosimetric parameters for the target volume, however. On the contrary, Hong-Wie Liu et al.  reported steadily decreasing numbers of patients with low D90s as their implant program matured. Keyes et al.  showed significantly falling acute urinary retention rates by order of implants. A learning curve could also be seen avoiding seed migration .
The aim of this study is to report our single-institution experience with BT for patients diagnosed with early-stage prostate cancer, highlight treatment related toxicities and analyze their relation to QoL.
Patients and methods
Mean ± SD
68.5 ± 5.6
PSA at diagnosis (ng/mL)
Mean ± SD
7.2 ± 2.6
10 or less
Clinical T stage
IPSS at baseline
Mean ± SD
6.3 ± 4.0 (*)
Follow-up period (months)
50 (1–85 months)
No. of pts.
Mean ± SD
Urethra D30 [Gy] at implantation (1)
185.5 ± 6.7
Prostate V [cc] at implantation (2)
31.9 ± 11.3
Prostate V [cc] postimplant (2)
31.8 ± 11.1
Prostate D90 [Gy] at implantation (3)
185.5 ± 4.0
Prostate D90 [Gy] postimplant (3)
179.2 ± 16.3
Prostate V100 [%] at implantation (4)
99.6 ± 0.5
Prostate V100 [%] postimplant (4)
94.9 ± 3.8
Prostate V90.6 [%] at implantation (5)
99.9 ± 0.2
Prostate V90.6 [%] postimplant (5)
97.0 ± 3.8
Rectum V100 [cc] at implantation (6)
0.3 ± 0.2
Rectum V100 [cc] postimplant (6)
0.5 ± 0.6
Data collection, management, analysis and visualization were performed with Microsoft Office Professional 2007 and IBM SPSS Statistics for Macintosh, Version 22.0. Armonk, NY: IBM Corp. P-values below 0.05 were considered statistically significant.
In order to reach a higher data quantity for a valid interpretation, an additional written survey was conducted. Of all patients, 111 returned completed questionnaires. Self-estimated QoL was correlated with health status, ICIQ, IIEF-5, IPSS and GI toxicity using Spearman’s rho. Moreover, all potentially influencing dosimetric and pre-therapeutic parameters were correlated with these outcome variables, e.g. the urethral D30, volume of the prostate and pre-therapeutic IPSS with ICIQ scores or, the rectal V100 and volume of the prostate with GI toxicity. The strength of correlation was interpreted as weak for ρ < 0.5, moderate for 0.5 ≤ ρ < 0.8 and strong for ρ > 0.8. As for interpretation of the IPSS, we followed the definition of an absolute rise in score of five points to represent clinically significant worsening in the patients’ urinary symptoms, as initially used and validated by Cesaretti et al. .
To determine whether there were differences between the implant qualities of the two surgeons, an unpaired t-test was employed. The tested variables are metric and the sample size is large enough. According to the central limit theorem, it can thus be employed without tests on normal distribution. To assess the equality of variances for all variables calculated for the two groups, Levene’s test was used.
To investigate a possible pattern of learning effects, the study population was divided into a group of 85 patients (early implantations) and 84 patients (late implantations), respectively. As depicted above, Levene’s and unpaired t-tests could be used for comparison. Included variables were the number of lost or dislocated seeds and the above-mentioned dosimetric parameters. Data were also evaluated separately for both surgeons.
For 105 men, grading of proctitis at 1.5 months after treatment was obtained, and at least another data point during further follow-up. Of these patients, 21% (n = 22) showed improvement of proctitis symptoms in follow-up. As many as 9.5% (n = 10) experienced worsening of associated complaints (nine patients with grade one and one patient with grade two morbidity).
Post-treatment changes in IPSS
No. of pts. (%)
IPSS (mean ± SD)
11.2 ± 5.1
≥ 5-point increase at 1.5 months
6.8 ± 3,3
≥ 5-point decrease after 1.5 months
4.6 ± 2.1
Pts. with PSA failure
Pts. with a follow-up more than 60 months
No. of pts. (%)
7.1 ± 2.5
6.3 ± 1.5
7.0 ± 2.5
0.4 ± 0.6
1.3 ± 1.6
0.1 ± 0.2
For a total of 164 patients, we were able to investigate the pattern of seed migration or loss. Most patients, n = 127 (75.6%), did not experience seed loss. The dislocation of a single seed was observed in 29 (17.7%) patients. Two seeds were lost in eight (4.9%), three in two (1.2%), and four in one of the patients. Predominant sites of migration/dislocation were to seminal vesicles, periprostatic tissues and lungs, occurring in 27, 13, and 10 patients, respectively. For one patient, a single seed that was lost could not be identified. Another patient lost a seed during urination. Furthermore, single seed embolization into the spinal canal, presacral space, and a deferent duct was observed in three patients (one patient for each site).
No. of pts.
Quality of life
Urethral D30 (3)
Volume of prostate
IPSS at survey
Due to the similar size of the referral base, many institutions in Germany as well as in other European countries offering BT have a comparable patient throughput. It is still important that patient series from smaller departments are analyzed to increase the quantity of comparable results, particularly since there are no randomized controlled studies to date that would permit an evidence-based assessment of the benefit of BT over other treatment options. In Germany, directives for the benefit catalogue of the statutory health insurance funds are issued by the G-BA (Federal Joint Board): Accordingly, there is no evidence regarding the patient-relevant endpoints, such as overall survival and diseases specific mortality. However, it has been stated that there is “some” evidence in terms of treatment toxicity: Rectal function may be more impaired when compared to EBRT, while sexual dysfunction and urinary incontinence may be less when compared to prostatectomy . A decision process regarding general coverage of BT has been suspended, providing that higher evidence by adequate studies is achieved. During the method evaluation process, BT is normally only funded by statutory insurances in a hospital setting. Exploitable results of larger prospective randomized trials, such as the German prostatic cancer study PREFERE , are expected.
Overall disease free survival at five years in patients after BT differ between 76-93% [35-37]. As with toxicity, the series with BT as a monotherapy are difficult to compare due to differences in the follow-up time and treatment regimens. Furthermore, divergent definitions for biochemical failure were chosen. In this study, the rate of biochemical failure according to the RTOG-ASTRO Phoenix Definition  was low. The five-year biochemical recurrence-free survival was 93% for patients with a follow up of at least 60 months or prior recurrent disease. The actual rate may be even higher. Many patients had low PSA-values upon follow-up but could not be included in the subgroup analysis, due to lacking further values. Despite the relatively small number of patients included, our results are encouraging and in line with results from above cited studies.
Figures 1, 2, 3 demonstrate a good outcome in our study population in terms of aspects related to QoL, except for sexual dysfunction. Voiding symptoms decreased over time. There was also a low rate of proctitis according to toxicity grading, and the majority of patients had no signs of urinary incontinence. Most patients stated being rather content, content or very content with QoL. Self-appraisal of QoL was associated most strongly with that of general health condition (ρ = 0.8) and weakly correlated with the ICIQ (ρ = −0.21) and IPSS (ρ = −0,20). There was no significant correlation between QoL, the rate of proctitis or the IIEF-5 score.
From experience, one of the reasons men seek implantation over surgery when considering their treatment options for early-stage prostate cancer is the potentially lower risk for ED. In this study, ED was assessed with the IIEF-5. ED was not associated with worsening of QoL. Explanations for this finding might include a declining sexual interest with age (mean: 68.5 years in this study) or acceptance of sexual dysfunction over time. Furthermore, the IIEF was not designed to assess the impact of ED on psychosocial outcomes that influence sexual function. In fact, it was developed primarily for use as an efficacy measure in clinical trials of ED . Its 5-item version is a simple office screening instrument to diagnose the presence and severity, with a focus only on erectile function and intercourse satisfaction . Moreover, male sexual dysfunction includes diminished libido or abnormal ejaculation, issues that are not addressed in the questionnaire. Various conditions are known to be associated with ED, such as cardiovascular disease, obesity, diabetes mellitus, certain drugs, or depression . In this study, patients with comorbidities were not excluded. Though representative for the general population, our data would not allow to clearly attribute the pattern of ED to BT.
Due to the anatomic proximity of the prostate to the urethra and bladder, both acute and late toxicity can be observed. Most patients develop an acute worsening of urinary symptoms, such as increased frequency, urgency, nocturia, etc. These symptoms resolve in most cases . We assessed urinary symptoms using the IPSS and observed an increase of ≥ five points in 59% of the patients, approximately six weeks post implant. Of these, 38% reached their baseline level. In a study by Keyes et al., similar results were found in 712 men with localized prostate cancer treated with an I-125 implant between 1998 and 2003 : By six weeks after treatment, most patients experienced an acute exacerbation of urinary symptoms, which was associated with an increase in the IPSS to a mean of approximately 19. Symptoms resolved within six months in 65% of cases and within one year in 91%. Associated factors included more baseline urinary symptoms and more intense symptoms in the immediate post-treatment period. In our patients, there was a weak correlation between the last retrieved IPSS and the pretherapeutic scores. Neither the size of the prostate nor the urethral D30 impacted the IPSS. Serious rectal injuries (fistula) are rare  and were not observed in our study. An accurate implant technique can minimize the radiation dose to the anterior rectal wall and brachytherapy-related bowel morbidity. This was shown, for instance, by Snyder et al. , who demonstrated a correlation between the V100 and the development of grade 2 proctitis: If ≤ 0.8 cc of rectal wall received 160 Gy, no proctitis developed. The likelihood increased to 5% in case ≤ 1.3 cc received 160 Gy. In our study, the incidence of proctitis complaints was low. There was no significant association with QoL and the incidence was not influenced by rectal dosimetric parameters.
After BT, loose seeds are particularly prone to loss and movement. The loss of multiple seeds can cause a substantial reduction of D90 coverage. Stranded seeds are less prone to be lost . A weak but statistically significant correlation between the number of lost seeds and dosimetric parameters (V100, D90) could also be shown in this study. The clinical implications of this are unclear. A prescription dose of 160 Gy to the prostate used to be the local standard during the first years of implantations, leaning upon a dose–response analysis by Stock et al. : They recommended a range of 140–160 Gy delivered to the prostate as defined by the D90. In practice however, many brachytherapists plan a higher dose  to compensate for edema or seed placement uncertainty and D90s from 180 to 200 Gy seem to be well tolerated with low risk of toxicity . As for the urethra, one may aim for an UV30 < 125%  or a D30 < 130% of the prescription dose when referred to GEC-ESTRO recommendations . At the rectum, the RV100 is ideally < 1 cc at day 1 dosimetry and < 1.3 cc at day 30 (due to the resolution of periprostatic edema and, thus, changing proximity) .
A thorough evaluation of differences between day 0 and post-implant dosimetry was beyond the scope of this work. Prostate edema after BT is well recognized and can result in a decrease in dose coverage . The extent and time course of prostate edema and its effect on dosimetry have been analyzed for example by Taussky et al.  In this study, we compared the dosimetric results of two experienced surgeons. Our analyses indicate a significant difference between the surgeons for urethral D30. However, both reached values within recommended constraints. For other planning parameters, for neither seed loss nor dislocation, no significant differences were found. Moreover, we looked at two different time periods to evaluate possible learning effects as described in the literature. Our observation of a learning curve for variables defining the quality of an implantation partially corroborates effects that were previously noted: Within our chosen observation periods, significant changes were demonstrated: Less seeds were lost or dislocated and values of V100 and D90 increased over time. A closer examination performed separately for the implanting physicians reveals a slightly different picture. Both surgeons reached a significantly improved rate of seed loss over time, whereas a significant increase of V100 was only observed for one. Despite these effects, the clinical relevance remains unknown. In terms of tumor control probability, the D90 is particularly important . Moreover, the V100 could be a good clinical indicator for a successful implant. As for D90, obtained values for the early 85 implants was 174.6 Gy and, 184.0 Gy for the succeeding 84 implants: again, both meeting the recommendations. Recording all parameters separately for different implantation teams served as an additional means of quality control. Though statistically significant, the differences of the implant quality were minor. As a matter of fact, a higher learning capacity or better manual skills could not be derived from our data. In most prostate LDR brachytherapy programs, it is seen that the implant quality increases with the number of procedures performed up to about 70 to 100 procedures [47,48]. However, technological advances have taken place and made the implantation procedure more precise .
BT constitutes one of many effective and safe treatment options for early-stage prostate cancer. The five-year biochemical relapse-free survival is excellent and treatment toxicity is favorable. However, treatment-related side effects, even when mild, have to be discussed with the patient. Quality of life and its related aspects are generally good. Learning effects by number of implants occur, but their impact on patient-relevant endpoints is inconclusive from our data.
We thank F. Klein for assistance with statistical analysis.
- Jemal A, Siegel R, Xu J, Ward E. Cancer statistics, 2010. CA Cancer J Clin. 2010;60:277–300.View ArticlePubMedGoogle Scholar
- Bestmann B, Loetters C, Diemer T, Weidner W, Küchler T, Rohde V. Prostate-specific symptoms of prostate cancer in a German general population. Prostate Cancer Prostatic Dis. 2007;10:52–9.View ArticlePubMedGoogle Scholar
- Stock RG, Stone NN, Cesaretti JA, Rosenstein BS. Biologically effective dose values for prostate brachytherapy: effects on PSA failure and posttreatment biopsy results. Int J Radiat Oncol Biol Phys. 2006;64:527–33.View ArticlePubMedGoogle Scholar
- Goldner G, Pötter R, Battermann JJ, Schmid MP, Kirisits C, Sljivic S, et al. Comparison of seed brachytherapy or external beam radiotherapy (70 Gy or 74 Gy) in 919 low-risk prostate cancer patients. Strahlenther Onkol. 2012;188:305–10.View ArticlePubMedGoogle Scholar
- Thompson I, Thrasher JB, Aus G, Burnett AL, Canby-Hagino ED, Cookson MS, et al. Guideline for the management of clinically localized prostate cancer: 2007 update. J Urol. 2007;177:2106–31.View ArticlePubMedGoogle Scholar
- Horwitz EM. American Brachytherapy Society: ABS brachytherapy consensus guidelines. Brachytherapy. 2012;11:4–5.View ArticlePubMedGoogle Scholar
- Salembier C, Lavagnini P, Nickers P, Mangili P, Rijnders A, Polo A, et al. Tumour and target volumes in permanent prostate brachytherapy: a supplement to the ESTRO/EAU/EORTC recommendations on prostate brachytherapy. Radiother Oncol. 2007;83(1):3–10. Epub 2007 Feb 26. PubMed PMID: 17321620.View ArticlePubMedGoogle Scholar
- Vikram B, Deore S, Beitler JJ, Sood B, Mullokandov E, Kapulsky A, et al. The relationship between dose heterogeneity (“hot” spots) and complications following high-dose rate brachytherapy. Int J Radiat Oncol Biol Phys. 1999;43:983–7.View ArticlePubMedGoogle Scholar
- Eshleman JS, Davis BJ, Pisansky TM, Wilson TM, Haddock MG, King BF, et al. Radioactive seed migration to the chest after transperineal interstitial prostate brachytherapy: extraprostatic seed placement correlates with migration. Int J Radiat Oncol Biol Phys. 2004;59:419–25.View ArticlePubMedGoogle Scholar
- Sugawara A, Nakashima J, Kunieda E, Nagata H, Mizuno R, Seki S, et al. Incidence of seed migration to the chest, abdomen, and pelvis after transperineal interstitial prostate brachytherapy with loose (125)I seeds. Radiat Oncol. 2011;6:130.View ArticlePubMed CentralPubMedGoogle Scholar
- Miura N, Kusuhara Y, Numata K, Shirato A, Hashine K, Sumiyoshi Y, et al. Radiation pneumonitis caused by a migrated brachytherapy seed lodged in the lung. Jpn J Clin Oncol. 2008;38:623–5.View ArticlePubMedGoogle Scholar
- Zhu AX, Wallner KE, Frivold GP, Ferry D, Jutzy KR, Foster GP. Prostate brachytherapy seed migration to the right coronary artery associated with an acute myocardial infarction. Brachytherapy. 2006;5:262–5.View ArticlePubMedGoogle Scholar
- Machtens S, Baumann R, Hagemann J, Warszawski A, Meyer A, Karstens JH, et al. Long-term results of interstitial brachytherapy (LDR-Brachytherapy) in the treatment of patients with prostate cancer. World J Urol. 2006;24:289–95.View ArticlePubMedGoogle Scholar
- Terk MD, Stock RG, Stone NN. Identification of patients at increased risk for prolonged urinary retention following radioactive seed implantation of the prostate. J Urol. 1998;160:1379–82.View ArticlePubMedGoogle Scholar
- Vijverberg PL, Blank LE, Dabhoiwala NF, de Reijke TM, Koedooder C, Hart AA, et al. Analysis of biopsy findings and implant quality following ultrasonically-guided 125I implantation for localised prostatic carcinoma. Br J Urol. 1993;72:470–7.View ArticlePubMedGoogle Scholar
- Merrick GS, Butler WM, Lief JH, Dorsey AT. Temporal resolution of urinary morbidity following prostate brachytherapy. Int J Radiat Oncol Biol Phys. 2000;47:121–8.View ArticlePubMedGoogle Scholar
- Gelblum DY, Potters L, Ashley R, Waldbaum R, Wang XH, Leibel S. Urinary morbidity following ultrasound-guided transperineal prostate seed implantation. Int J Radiat Oncol Biol Phys. 1999;45:59–67.View ArticlePubMedGoogle Scholar
- Blasko JC, Ragde H, Grimm PD. Transperineal ultrasound-guided implantation of the prostate: morbidity and complications. Scand J Urol Nephrol Suppl. 1991;137:113–8.PubMedGoogle Scholar
- Nag S, Scaperoth DD, Badalament R, Hall SA, Burgers J. Transperineal palladium 103 prostate brachytherapy: analysis of morbidity and seed migration. Urology. 1995;45:87–92.View ArticlePubMedGoogle Scholar
- Beyer DC, Priestley JB. Biochemical disease-free survival following 125I prostate implantation. Int J Radiat Oncol Biol Phys. 1997;37:559–63.View ArticlePubMedGoogle Scholar
- Hu K, Wallner K. Clinical course of rectal bleeding following I-125 prostate brachytherapy. Int J Radiat Oncol Biol Phys. 1998;41:263–265.22.View ArticlePubMedGoogle Scholar
- Sanda MG, Dunn RL, Michalski J, Sandler HM, Northouse L, Hembroff L, et al. Quality of life and satisfaction with outcome among prostate-cancer survivors. N Engl J Med. 2008;358(12):1250–61. doi:10.1056/NEJMoa074311. PubMed PMID: 18354103.View ArticlePubMedGoogle Scholar
- Le Fur E, Malhaire JP, Baverez D, Delage F, Perrouin-Verbe MA, Schlurmann F, et al. Impact of learning curve and technical changes on dosimetry in low-dose brachytherapy for prostate cancer. Strahlenther Onkol. 2012;188:1091–5.View ArticlePubMedGoogle Scholar
- Liu H-W, Malkoske K, Sasaki D, Bews J, Demers A, Nugent Z, et al. The dosimetric quality of brachytherapy implants in patients with small prostate volume depends on the experience of the brachytherapy team. Brachytherapy. 2010;9:202–7.View ArticlePubMedGoogle Scholar
- Keyes M, Schellenberg D, Moravan V, McKenzie M, Agranovich A, Pickles T, et al. Decline in urinary retention incidence in 805 patients after prostate brachytherapy: the effect of learning curve? Int J Radiat Oncol Biol Phys. 2006;64:825–34.View ArticlePubMedGoogle Scholar
- Taussky D, Moumdjian C, Larouche R, Béliveau-Nadeau D, Boudreau C, Hervieux Y, et al. Seed migration in prostate brachytherapy depends on experience and technique. Brachytherapy. 2012;11:452–6.View ArticlePubMedGoogle Scholar
- Barry MJ, Fowler FJ, O’Leary MP, Bruskewitz RC, Holtgrewe HL, Mebust WK, et al. The American Urological Association symptom index for benign prostatic hyperplasia. The Measurement Committee of the American Urological Association. J Urol. 1992;148:1549–57. discussion 1564.PubMedGoogle Scholar
- Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, et al. The European organization for research and treatment of cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85:365–76.View ArticlePubMedGoogle Scholar
- Avery K, Donovan J, Peters TJ, Shaw C, Gotoh M, Abrams P. ICIQ: a brief and robust measure for evaluating the symptoms and impact of urinary incontinence. Neurourol Urodyn. 2004;23:322–30.View ArticlePubMedGoogle Scholar
- Rosen RC, Cappelleri JC, Smith MD, Lipsky J, Peña BM. Development and evaluation of an abridged, 5-item version of the International Index of Erectile Function (IIEF-5) as a diagnostic tool for erectile dysfunction. Int J Impot Res. 1999;11:319–26.View ArticlePubMedGoogle Scholar
- Cesaretti JA, Stone NN, Stock RG. Urinary symptom flare following I-125 prostate brachytherapy. Int J Radiat Oncol Biol Phys. 2003;56:1085–92.View ArticlePubMedGoogle Scholar
- Roach M, Hanks G, Thames H, Schellhammer P, Shipley WU, Sokol GH, et al. Defining biochemical failure following radiotherapy with or without hormonal therapy in men with clinically localized prostate cancer: recommendations of the RTOG-ASTRO phoenix consensus conference. In Int J Radiat Oncol Biol Phys Volume. 2006;65:965–74.View ArticleGoogle Scholar
- Interstitielle Brachytherapie beim lokal begrenzten Prostatakarzinom. [www.g-ba.de]
- Stöckle M, Bussar-Maatz R. [Localised prostate cancer: the PREFERE trial]. Z Evid Fortbild Qual Gesundhwes. 2012;106:333–5. discussion 335.View ArticlePubMedGoogle Scholar
- Blasko JC, Wallner K, Grimm PD, Ragde H. Prostate specific antigen based disease control following ultrasound guided 125iodine implantation for stage T1/T2 prostatic carcinoma. J Urol. 1995;154:1096–9.View ArticlePubMedGoogle Scholar
- Brachman DG, Thomas T, Hilbe J, Beyer DC. Failure-free survival following brachytherapy alone or external beam irradiation alone for T1-2 prostate tumors in 2222 patients: results from a single practice. Int J Radiat Oncol Biol Phys. 2000;48:111–7.View ArticlePubMedGoogle Scholar
- Beyer DC, Thomas T, Hilbe J, Swenson V. Relative influence of Gleason score and pretreatment PSA in predicting survival following brachytherapy for prostate cancer. Brachytherapy. 2003;2:77–84.View ArticlePubMedGoogle Scholar
- Rosen RC, Riley A, Wagner G, Osterloh IH, Kirkpatrick J, Mishra A. The international index of erectile function (IIEF): a multidimensional scale for assessment of erectile dysfunction. Urology. 1997;49:822–30.View ArticlePubMedGoogle Scholar
- Rosen RC, Fisher WA, Eardley I, Niederberger C, Nadel A, Sand M, et al. The multinational Men’s Attitudes to Life Events and Sexuality (MALES) study: I. Prevalence of erectile dysfunction and related health concerns in the general population. Curr Med Res Opin. 2004;20:607–17.View ArticlePubMedGoogle Scholar
- Keyes M, Miller S, Moravan V, Pickles T, Liu M, Spadinger I, et al. Urinary symptom flare in 712 125I prostate brachytherapy patients: long-term follow-up. Int J Radiat Oncol Biol Phys. 2009;75:649–55.View ArticlePubMedGoogle Scholar
- Stone NN, Stock RG. Complications following permanent prostate brachytherapy. Eur Urol. 2002;41:427–33.View ArticlePubMedGoogle Scholar
- Snyder KM, Stock RG, Hong SM, Lo YC, Stone NN. Defining the risk of developing grade 2 proctitis following 125I prostate brachytherapy using a rectal dose-volume histogram analysis. Int J Radiat Oncol Biol Phys. 2001;50:335–41.View ArticlePubMedGoogle Scholar
- Reed DR, Wallner KE, Merrick GS, Arthurs S, Mueller A, Cavanagh W, et al. A prospective randomized comparison of stranded vs. loose 125I seeds for prostate brachytherapy. Brachytherapy. 2007;6:129–34.View ArticlePubMedGoogle Scholar
- Stock RG, Stone NN, Tabert A, Iannuzzi C, DeWyngaert JK. A dose–response study for I-125 prostate implants. Int J Radiat Oncol Biol Phys. 1998;41:101–8.View ArticlePubMedGoogle Scholar
- Gómez-Iturriaga Piña A, Crook J, Borg J, Ma C. Biochemical disease-free rate and toxicity for men treated with iodine-125 prostate brachytherapy with d(90) ≥180 Gy. Int J Radiat Oncol Biol Phys. 2010;78:422–7.View ArticlePubMedGoogle Scholar
- Taussky D, Austen L, Toi A, Yeung I, Williams T, Pearson S, et al. Sequential evaluation of prostate edema after permanent seed prostate brachytherapy using CT-MRI fusion. Int J Radiat Oncol Biol Phys. 2005;62:974–80.View ArticlePubMedGoogle Scholar
- Nag S, Bice W, DeWyngaert K, Prestidge B, Stock R, Yu Y. The American Brachytherapy Society recommendations for permanent prostate brachytherapy postimplant dosimetric analysis. Int J Radiat Oncol Biol Phys. 2000;46(1):221–30. Review. PubMed PMID: 10656396.View ArticlePubMedGoogle Scholar
- Beaulieu L, Evans D-AR, Aubin S, Angyalfi S, Husain S, Kay I, et al. Bypassing the learning curve in permanent seed implants using state-of-the-art technology. Int J Radiat Oncol Biol Phys. 2007;67:71–7.View ArticlePubMedGoogle Scholar
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.