Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan
Department of Urology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Anticancer Res. 2022 Apr;42(4):2123-2130. doi: 10.21873/anticanres.15694.
Despite the rapid introduction of androgen receptor-targeted agents (ARTA) into clinical practice for castration-resistant prostate cancer (CRPC), the optimal treatment strategy after first-line ARTA remains unclear. The object of this study was to clarify clinical outcomes of second-line therapy for CRPC after first-line ARTA.
The medical records of 130 consecutive patients with CRPC with disease progression during first-line ARTA and who started second-line therapy at our Institution between 2014 and 2020 were analyzed.
A total of 130 patients with CRPC were identified. Ninety patients underwent ARTA-ARTA treatment, and 40 patients underwent ARTA-docetaxel treatment. The median observation period after second-line ARTA or docetaxel administration was 14.2 months. The prostate-specific antigen response rates overall, and after second-line ARTA, and docetaxel were 26.8%, 24.7%, and 31.6%, respectively. The median progression-free survival (PFS) and 1- and 2-year PFS rates of second-line therapy were 7.9 months and 34.6% and 15.4%, respectively. The median overall survival (OS) and 1- and 2-year OS rates were 27.4 months and 81.8%, and 54.9%, respectively. Multivariate analyses for OS disclosed that a C-reactive protein over the upper limit of normal and time from first-line ARTA to progression under 12 months were associated with shorter OS. Prostate-specific antigen response, PFS and OS of second-line therapy were not significantly different between second-line ARTA and docetaxel.
There was no significant difference in OS between ARTA-ARTA and ARTA-docetaxel groups in the present study, suggesting that second-line ARTA might be the preferred treatment after initial failure of ARTA.
尽管雄激素受体靶向药物(ARTA)在去势抵抗性前列腺癌(CRPC)的临床实践中迅速引入,但一线 ARTA 后最佳的治疗策略仍不清楚。本研究旨在阐明一线 ARTA 后 CRPC 二线治疗的临床结果。
分析了 2014 年至 2020 年间在我院接受一线 ARTA 期间疾病进展并开始二线治疗的 130 例连续 CRPC 患者的病历。
共确定了 130 例 CRPC 患者。90 例患者接受了 ARTA-ARTA 治疗,40 例患者接受了 ARTA-多西他赛治疗。二线 ARTA 或多西他赛给药后中位观察期为 14.2 个月。二线治疗后的前列腺特异性抗原(PSA)反应率、二线 ARTA 治疗后和多西他赛治疗后的 PSA 反应率分别为 26.8%、24.7%和 31.6%。二线治疗的中位无进展生存期(PFS)和 1 年和 2 年 PFS 率分别为 7.9 个月、34.6%和 15.4%。中位总生存期(OS)和 1 年和 2 年 OS 率分别为 27.4 个月、81.8%和 54.9%。OS 的多变量分析显示,C 反应蛋白超过正常值上限和一线 ARTA 至进展时间不足 12 个月与 OS 较短相关。二线 ARTA 和多西他赛的二线治疗的 PSA 反应、PFS 和 OS 无显著差异。
在本研究中,二线 ARTA-ARTA 和 ARTA-多西他赛组之间的 OS 无显著差异,表明二线 ARTA 可能是一线 ARTA 治疗失败后的首选治疗方法。