Zumsteg Zachary S, Chen Zinan, Howard Lauren E, Amling Christopher L, Aronson William J, Cooperberg Matthew R, Kane Christopher J, Terris Martha K, Spratt Daniel E, Sandler Howard M, Freedland Stephen J
Samuel Oschin Comprehensive Cancer Institute, Cedars-Sinai Medical Center, Los Angeles, California.
Department of Radiation Oncology, Cedars-Sinai Medical Center, Los Angeles, California.
Prostate. 2017 Dec;77(16):1592-1600. doi: 10.1002/pros.23436. Epub 2017 Oct 10.
Prostate cancer is a heterogeneous disease, and risk stratification systems have been proposed to guide treatment decisions. However, significant heterogeneity remains for those with unfavorable-risk disease.
This study included 3335 patients undergoing radical prostatectomy without adjuvant radiotherapy in the SEARCH database. High-risk patients were dichotomized into standard and very high-risk (VHR) groups based on primary Gleason pattern, percentage of positive biopsy cores (PPBC), number of NCCN high-risk factors, and stage T3b-T4 disease. Similarly, intermediate-risk prostate cancer was separated into favorable and unfavorable groups based on primary Gleason pattern, PPBC, and number of NCCN intermediate-risk factors.
Median follow-up was 78 months. Patients with VHR prostate cancer had significantly worse PSA relapse-free survival (PSA-RFS, P < 0.001), distant metastasis (DM, P = 0.004), and prostate cancer-specific mortality (PCSM, P = 0.015) in comparison to standard high-risk (SHR) patients in multivariable analyses. By contrast, there was no significant difference in PSA-RFS, DM, or PCSM between SHR and unfavorable intermediate-risk (UIR) patients. Therefore, we propose a novel risk stratification system: Group 1 (low-risk), Group 2 (favorable intermediate-risk), Group 3 (UIR and SHR), and Group 4 (VHR). The c-index of this new grouping was 0.683 for PSA-RFS and 0.800 for metastases, compared to NCCN-risk groups which yield 0.666 for PSA-RFS and 0.764 for metastases.
Patients classified as VHR have markedly increased rates of PSA relapse, DM, and PCSM in comparison to SHR patients, whereas UIR and SHR patients have similar prognosis. Novel therapeutic strategies are needed for patients with VHR, likely involving multimodality therapy.
前列腺癌是一种异质性疾病,已经提出了风险分层系统来指导治疗决策。然而,对于那些具有不良风险疾病的患者,仍存在显著的异质性。
本研究纳入了SEARCH数据库中3335例接受根治性前列腺切除术且未接受辅助放疗的患者。高危患者根据主要 Gleason 模式、阳性活检核心百分比(PPBC)、NCCN 高危因素数量以及T3b - T4期疾病分为标准高危组和极高危(VHR)组。同样,中危前列腺癌根据主要 Gleason 模式、PPBC和NCCN中危因素数量分为有利组和不利组。
中位随访时间为78个月。在多变量分析中,与标准高危(SHR)患者相比,VHR前列腺癌患者的无PSA复发生存率(PSA - RFS,P < 0.001)、远处转移(DM,P = 0.004)和前列腺癌特异性死亡率(PCSM,P = 0.015)显著更差。相比之下,SHR患者和不利中危(UIR)患者之间的PSA - RFS、DM或PCSM没有显著差异。因此,我们提出了一种新的风险分层系统:第1组(低危)、第2组(有利中危)、第3组(UIR和SHR)和第4组(VHR)。与NCCN风险组相比,这种新分组的PSA - RFS的c指数为0.683,转移的c指数为0.800,而NCCN风险组的PSA - RFS为0.666,转移为0.764。
与SHR患者相比,被归类为VHR的患者的PSA复发、DM和PCSM发生率显著增加,而UIR和SHR患者的预后相似。VHR患者需要新的治疗策略,可能涉及多模式治疗。