Low-dose rate brachytherapy for patients with low or intermediate-risk prostate cancer. Analysis of relapse-free survival

2019 ◽  
Vol 11 (2) ◽  
pp. 44-49
Author(s):  
V.A. Solodky ◽  
◽  
A.Yu. Pavlov ◽  
A.D. Tsybulskiy ◽  
A.S. Pchelintsev ◽  
...  
2020 ◽  
Author(s):  
Zhien Zhou ◽  
Meiting He ◽  
Yi Zhou ◽  
Weigang Yan ◽  
Xingcheng Wu ◽  
...  

Abstract Background: Radical prostatectomy (RP) and low-dose-rate brachytherapy (LDR) are two widely used treatment options for patients with intermediate-risk prostate cancer (IRPC). However, which one is better remains controversial. Therefore, the purpose of this study was to compare the efficacy of RP vs LDR for patients with IRPC. Methods: A retrospective analysis was performed on 361 IRPC patients who underwent treatment from January 2010 and August 2017. 160 underwent RP and 201 underwent LDR using Iodine-125. Biochemical failure for RP was defined as prostate-specific antigen (PSA) levels > 0.2 ng/ml, and for LDR as nadir PSA level + 2 ng/ml. The log-rank test compared biochemical relapse-free survival (bRFS) between the two modalities, and Cox regression identified factors associated with bRFS. Results: Median follow-up was 54 months for RP and 69 months for LDR. The 5-and 8-year bRFS rates were 70.2% and 63.1% in the RP group, and 83.2% and 68.9% in the LDR group, respectively, P=0.003. There were no significant differences in terms of clinical relapse-free survival (cRFS), cancer-specific survival (CSS) or overall survival (OS) between the two groups. Conclusion: LDR is a reasonable treatment option for IRPC patients, yielding improved bRFS and equivalent rates of cRFS, CSS and OS compared with RP.


2021 ◽  
Author(s):  
Zhien Zhou ◽  
Zhen Liang ◽  
Yi Zhou ◽  
Weigang Yan ◽  
Xingcheng Wu ◽  
...  

Abstract Objective: To compare the efficacy of radical prostatectomy vs low-dose-rate brachytherapy for patients with intermediate-risk prostate cancer.Materials and methods: A retrospective analysis was performed on 361 intermediate-risk prostate cancer patients who underwent treatment from January 2010 and August 2019. 160 underwent radical prostatectomy and 201 underwent low-dose-rate brachytherapy using Iodine-125. Biochemical failure for radical prostatectomy was defined as prostate-specific antigen levels > 0.2 ng/ml, and for low-dose-rate brachytherapy as nadir PSA level + 2 ng/ml. The log-rank test compared biochemical relapse-free survival between the two modalities, and Cox regression identified factors associated with biochemical relapse-free survival.Results: Median follow-up was 54 months for radical prostatectomy and 69 months for low-dose-rate brachytherapy. The 5-and 8-year biochemical relapse-free survival rates were 70.2% and 63.1% in the radical prostatectomy group, and 83.2% and 68.9% in the low-dose-rate brachytherapy group, respectively, P=0.003. There were no significant differences in terms of clinical relapse-free survival, cancer-specific survival or overall survival between the two groups. Conclusion: Low-dose-rate brachytherapy is a reasonable treatment option for intermediate-risk prostate cancer patients, yielding improved biochemical relapse-free survival and equivalent rates of clinical relapse-free survival, cancer-specific survival and overall survival compared with radical prostatectomy.


Cancer ◽  
2012 ◽  
Vol 119 (8) ◽  
pp. 1537-1546 ◽  
Author(s):  
W. James Morris ◽  
Mira Keyes ◽  
Ingrid Spadinger ◽  
Winkle Kwan ◽  
Mitchell Liu ◽  
...  

2017 ◽  
Vol 98 (1) ◽  
pp. 101-107 ◽  
Author(s):  
Matthew M. Gestaut ◽  
Wendi Cai ◽  
Shilpa Vyas ◽  
Belur J. Patel ◽  
Salman A. Hasan ◽  
...  

2013 ◽  
Vol 7 (5-6) ◽  
pp. 411 ◽  
Author(s):  
George Rodrigues ◽  
Xiaomei Yao ◽  
D. Andrew Loblaw ◽  
Michael Brundage ◽  
Joseph L. Chin

Objective: The Genitourinary Cancer Disease Site Group (GUDSG) and Cancer Care Ontario’s Program in Evidence-Based Care (PEBC) in Ontario, Canada developed a guideline on low-dose rate brachytherapy (LDR-BT) in patients with early-stage low-grade prostate cancer in 2001. The current updated guideline focuses on the research questions regarding the effect of LDR-BT alone, the effect of LDR-BT with external beam radiation therapy (EBRT) and the selection of an isotope.Methods: This guideline was developed by using the methods of the Practice Guidelines Development Cycle and the core methodology was a systematic review. MEDLINE and EMBASE (from January 1996 to October 2011), the Cochrane Library, main guideline websites, and main annual meeting abstract websites specific for genitourinary diseases were searched. Internal and external reviews of the draft guideline were conducted.Results: The draft guideline was developed according to a total of 10 systematic reviews and 55 full text articles that met the preplanned study selection criteria. The quality of evidence was low to moderate. The final report reflects integration of the feedback obtained through the internal review (two oncologists and a methodologist) and external review (five target reviewers and 48 professional consultation reviewers) process, with final approval given by the GU DSG and the PEBC.Conclusion: The main recommendations are: (1) For patients with newly diagnosed low-risk or intermediate-risk prostate cancer who require or choose active treatment, LDR-BT alone is a treatment option as an alternative to EBRT alone or RP alone; and (2) I-125 and Pd-103 are each reasonable isotope options.


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