department of Integrative Cancer Therapy and Urology, Kanazawa University Graduate School of Medical Science, Kanazawa, Japan.
Department of Functional Imaging and Artificial Intelligence, Kanazawa University, Kanazawa, Japan.
Anticancer Res. 2022 Jun;42(6):3099-3108. doi: 10.21873/anticanres.15798.
BACKGROUND/AIM: This study aimed to evaluate the therapeutic benefit of novel androgen receptor-targeted agents (ARTAs) in castration-resistant prostate cancer (CRPC) with bone metastases in Japan.
In followup to our prospective observational study (PROSTAT-BSI) from 2012 to 2018 on metastatic hormone-sensitive prostate cancer (mHSPC) and metastatic CRPC (mCRPC) before docetaxel initiation, we conducted this sub-analysis to investigate the benefit of ARTAs after clinical recurrence on overall survival (OS) in the real-world clinical setting in Japan. In this study, we compared patients who were treated with ARTA with those who received only vintage hormone therapy including docetaxel after clinical recurrence.
In the mHSPC group, 69 patients became mCRPC and were treated with or without ARTAs. No significant difference was observed in prostate-specific antigen (PSA) progression-free survival between the ARTA (+) and ARTA (-) groups; however, OS after clinical recurrence was significantly better in the ARTA (+) group than in the ARTA (-) group (median OS 31.9 vs. 23.0 months; p<0.01).
The ARTAs are beneficial even after mHSPC recurrence in Japanese patients in the real-world clinical setting. Since ARTAs are beneficial after clinical recurrence, it may be better to switch to ARTAs whenever necessary based on PSA response after combined androgen blockade therapy, considering the adverse effects and cost. This approach may be suitable to reduce overtreatment in Japanese patients with mHSPC.
背景/目的:本研究旨在评估新型雄激素受体靶向药物(ARTAs)在日本伴骨转移的去势抵抗性前列腺癌(CRPC)中的治疗获益。
在我们 2012 年至 2018 年对起始多西他赛治疗前转移性激素敏感性前列腺癌(mHSPC)和转移性 CRPC(mCRPC)的前瞻性观察性研究(PROSTAT-BSI)随访中,我们进行了这项亚分析,以研究在日本真实临床环境中,ARTAs 在临床复发后对总生存(OS)的获益。在这项研究中,我们比较了在临床复发后接受 ARTA 治疗与仅接受包括多西他赛在内的传统激素治疗的患者。
在 mHSPC 组中,69 例患者进展为 mCRPC,并接受或未接受 ARTA 治疗。ARTA(+)组和 ARTA(-)组的前列腺特异性抗原(PSA)无进展生存无显著差异;然而,ARTA(+)组的 OS 明显优于 ARTA(-)组(中位 OS 31.9 个月 vs. 23.0 个月;p<0.01)。
在真实临床环境中,ARTAs 对日本患者即使在 mHSPC 复发后也有益。由于在临床复发后 ARTAs 有益,因此在联合雄激素阻断治疗后根据 PSA 反应,可能需要时随时切换至 ARTA,考虑到不良反应和成本。这种方法可能适合减少日本 mHSPC 患者的过度治疗。