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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

机译:根治性前列腺切除术患者的阳性手术切缘不能预测长期肿瘤学结果:来自共享平等接入区域癌症医院(sEaRCH)队列的结果

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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 \u3e 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 \u3c /= 0.001). After adjusting for demographic and pathological characteristics, PSMs were associated with increased risk of only BCR (HR 1.98, P \u3c 0.001), and not CRPC, metastases, or PCSM (HR \u3c /=1.29, P \u3e 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.
机译:目的:评估积极的手术切缘(PSM)对根治性前列腺切除术(RP)术后长期结局的影响,包括转移,去势抵抗性前列腺癌(CRPC)和前列腺癌特异性死亡率(PCSM)。 :从1988年至2013年在RP治疗的共享均等访问区域癌症医院(SEARCH)队列中对4 051名男性进行了回顾性研究。在预测生化复发(BCR),CRPC时,使用比例风险模型估算PSM的风险比(HRs) ,转移和PCSM。为了确定PSM在某些患者中是否更具预测性,通过病理Gleason评分,分期和术前前列腺特异性抗原(PSA)水平进行分析。结果:中位(四分位间距)随访为6.6(3.2-10.6)年和1 127名患者接受了10年的随访。在此期间,有302名(32%)的男性患有BCR,112名(3%)患有CRPC,144名(4%)发生了转移,而83名(2%)因前列腺癌死亡。有1600名(40%)患有PSM的男性。在未经校正的模型中,PSM与所有不良结局均显着相关:BCR,CRPC,转移灶和PCSM(均P \ u3c / = 0.001)。在调整了人口统计学和病理学特征后,PSM与仅BCR(HR 1.98,P <0.001)而不与CRPC,转移瘤或PCSM(HR \ u3c /=1.29,P \ u3e 0.18)的风险增加相关。当按病理学Gleason评分,分期或PSA水平进行分层以及排除接受辅助放疗的患者时,也观察到相似的结果。结论:RP后的PSM并不是整体或任何亚组CRPC,转移或PCSM的独立危险因素。在没有其他高风险特征的情况下,单独的PSM可能不能作为辅助放疗的指征。

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