Positive surgical margins in radical prostatectomy patients do not predict long‐term oncological outcomes: results from the Shared Equal Access Regional Cancer Hospital (SEARCH) cohort. (23rd June 2015)

• Record Type: Journal Article
• Authors: Mithal, Prabhakar; Howard, Lauren E.; Aronson, William J.; Terris, Martha K.; Cooperberg, Matthew R.; Kane, Christopher J.; Amling, Christopher; Freedland, Stephen J.
• Is Part Of: BJU international. Volume 117:Number 2(2016:Jan.)
• Page Start: 244
• Page End: 248
• Publication Date: 2015-06-23
• Subjects: prostate cancer -- prostatectomy -- adjuvant radiotherapy -- disease progression; Genitourinary organs -- Diseases -- Periodicals; Genitourinary organs -- Surgery -- Periodicals; Urology -- Periodicals; 616.6
• DOI: 10.1111/bju.13181
• Languages: English
• ISSNs: 1464-4096

Abstract

Abstract : Objective: To assess the impact of positive surgical margins (PSMs) on long‐term outcomes after radical prostatectomy (RP), including metastasis, castrate‐resistant prostate cancer (CRPC), and prostate cancer‐specific mortality (PCSM). Patients and Methods: Retrospective study of 4 051 men in the Shared Equal Access Regional Cancer Hospital (SEARCH) cohort treated by RP from 1988 to 2013. Proportional hazard models were used to estimate hazard ratios (HRs) of PSMs in predicting biochemical recurrence (BCR), CRPC, metastases, and PCSM. To determine if PSMs were more predictive in certain patients, analyses were stratified by pathological Gleason score, stage, and preoperative prostate‐specific antigen (PSA) level. Results: The median (interquartile range) follow‐up was 6.6 (3.2–10.6) years and 1 127 patients had >10 years of follow‐up. During this time, 302 (32%) men had BCR, 112 (3%) developed CRPC, 144 (4%) developed metastases, and 83 (2%) died from prostate cancer. There were 1 600 (40%) men with PSMs. In unadjusted models, PSMs were significantly associated with all adverse outcomes: BCR, CRPC, metastases and PCSM (all P ≤ 0.001). After adjusting for demographic and pathological characteristics, PSMs were associated with increased risk of only BCR (HR 1.98, P < 0.001), and not CRPC, metastases, or PCSM (HR ≤1.29, P > 0.18). Similar results were seen when stratified by pathological Gleason score, stage, or PSA level, and when patients who underwent adjuvant radiotherapy were excluded. Conclusions: PSMs after RP are not an independent risk factor for CRPC, metastasis, or PCSM overall or within any subset. In the absence of other high‐risk features, PSMs alone may not be an indication for adjuvant radiotherapy.