Division of Medical Oncology, University of Colorado Cancer Center, Aurora, CO.
Biostatistics and Bioinformatics, University of Colorado Cancer Center Biostatistics Core, Aurora, CO.
Clin Genitourin Cancer. 2023 Aug;21(4):483-490. doi: 10.1016/j.clgc.2023.04.008. Epub 2023 Apr 24.
De novo neuroendocrine prostate cancer (NEPC) and treatment-emergent neuroendocrine prostate cancer (T-NEPC) are rare diseases with a poor prognosis. After first-line platinum chemotherapy, there is no consensus on second-line treatments.
Patients with a pathologic diagnosis of de novo NEPC or T-NEPC between 2000 and 2020 who received first-line platinum and any second-line systemic therapy were selected and standardized clinical data was collected via the electronic health record at each institution. The primary endpoint was overall survival (OS) based on second-line therapy. Secondary endpoints included objective response rate (ORR) to second-line therapy, PSA response, and time on treatment.
Fifty-eight patients (32 de novo NEPC, 26 T-NEPC) from 8 institutions were included. At de novo NEPC or T-NEPC diagnosis, the overall cohort had a median age of 65.0 years (IQR 59.2-70.3) and median PSA of 3.0 ng/dL (IQR 0.6-17.9). Following first-line platinum chemotherapy, 21 patients (36.2%) received platinum chemotherapy, 10 (17.2%) taxane monotherapy, 11 (19.0%) immunotherapy, 10 (17.2%) other chemotherapy, and 6 (16.2%) other systemic therapy. Among 41 evaluable patients, the ORR was 23.5%. The mOS after start of second-line therapy was 7.4 months (95% CI 6.1-11.9).
In this retrospective study, patients with de novo NEPC or T-NEPC who received second-line therapy were treated with wide variety of treatment regimens, reflecting the lack of consensus in this setting. Most patients received chemotherapy-based treatments. Overall prognosis was poor and ORR was low in the second line regardless of treatment choice.
新发神经内分泌前列腺癌(NEPC)和治疗后出现的神经内分泌前列腺癌(T-NEPC)是罕见疾病,预后较差。在接受一线铂类化疗后,二线治疗尚无共识。
选择了 2000 年至 2020 年间经病理诊断为新发 NEPC 或 T-NEPC 并接受一线铂类药物和任何二线全身治疗的患者,并通过每个机构的电子病历收集了标准化的临床数据。主要终点是基于二线治疗的总生存期(OS)。次要终点包括二线治疗的客观缓解率(ORR)、PSA 反应和治疗时间。
来自 8 个机构的 58 名患者(32 名新发 NEPC,26 名 T-NEPC)被纳入研究。在新发 NEPC 或 T-NEPC 诊断时,整个队列的中位年龄为 65.0 岁(IQR 59.2-70.3),中位 PSA 为 3.0ng/dL(IQR 0.6-17.9)。一线铂类化疗后,21 名患者(36.2%)接受了铂类化疗,10 名(17.2%)接受了紫杉醇单药治疗,11 名(19.0%)接受了免疫治疗,10 名(17.2%)接受了其他化疗,6 名(16.2%)接受了其他全身治疗。在 41 名可评估患者中,ORR 为 23.5%。二线治疗开始后的 mOS 为 7.4 个月(95%CI 6.1-11.9)。
在这项回顾性研究中,接受二线治疗的新发 NEPC 或 T-NEPC 患者接受了多种治疗方案治疗,反映出该治疗方案缺乏共识。大多数患者接受了基于化疗的治疗。无论治疗选择如何,二线治疗的总体预后均较差,ORR 较低。