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根治性前列腺切除术后切缘阳性患者发生全身进展和前列腺癌死亡的临床病理预测因素。

Clinicopathological predictors of systemic progression and prostate cancer mortality in patients with a positive surgical margin at radical prostatectomy.

机构信息

Department of Urology, Mayo Medical School and Mayo Clinic, Rochester, MN, USA.

出版信息

Prostate Cancer Prostatic Dis. 2012 Mar;15(1):56-62. doi: 10.1038/pcan.2011.36. Epub 2011 Aug 2.

Abstract

BACKGROUND

Although a positive surgical margin (PSM) at radical prostatectomy (RRP) has been consistently linked to an increased risk of biochemical recurrence, the impact of margin status on patient survival continues to be debated. We evaluated long-term outcomes of patients with a PSM at RRP and determined predictors of systemic progression (SP) and mortality in these men.

METHODS

We reviewed our institutional registry of 16,749 patients who underwent RRP between 1990 and 2008 to identify 2895 patients with a PSM. Median follow-up was 10.6 years. Postoperative survival was estimated using the Kaplan-Meier method. Cox proportional hazard regression models were used to analyze clinicopathological variables associated with SP and death from prostate cancer.

RESULTS

A 15-year SP-free and cancer-specific survival was 90 and 93%, respectively. On multivariate analysis, higher tumor volume, increased pathological Gleason score and advanced pathological tumor stage were associated with significantly increased risks of SP and death from prostate cancer, whereas number and location of PSM did not predict mortality.

CONCLUSIONS

The risks of SP and prostate cancer death in patients with a PSM remain low on long-term follow-up. Tumor variables are the primary determinants of cancer death. These results should be considered when evaluating patients with a PSM for adjuvant therapy.

摘要

背景

尽管根治性前列腺切除术(RRP)中的阳性切缘(PSM)与生化复发风险增加一致相关,但切缘状态对患者生存的影响仍存在争议。我们评估了在 RRP 中存在 PSM 的患者的长期结局,并确定了这些患者发生全身进展(SP)和死亡的预测因素。

方法

我们回顾了我们机构 1990 年至 2008 年接受 RRP 的 16749 例患者的登记处,以确定 2895 例存在 PSM 的患者。中位随访时间为 10.6 年。使用 Kaplan-Meier 方法估计术后生存。使用 Cox 比例风险回归模型分析与 SP 和前列腺癌相关的临床病理变量。

结果

15 年无 SP 和癌症特异性生存率分别为 90%和 93%。多变量分析显示,肿瘤体积较大、病理 Gleason 评分增加和病理肿瘤分期较晚与 SP 和前列腺癌死亡风险显著增加相关,而 PSM 的数量和位置并不能预测死亡率。

结论

在长期随访中,存在 PSM 的患者发生 SP 和前列腺癌死亡的风险仍然较低。肿瘤变量是癌症死亡的主要决定因素。在评估 PSM 患者是否接受辅助治疗时,应考虑这些结果。

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