Department of Urology, Japanese Red Cross Otsu Hospital, 1 Chome-1-35 Nagara, Otsu, Shiga, 520-0046, Japan.
Department of Urology, Kyoto University Graduate School of Medicine, 54 Shogoinkawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Int J Clin Oncol. 2024 Oct;29(10):1564-1573. doi: 10.1007/s10147-024-02597-x. Epub 2024 Aug 17.
This retrospective observational study explored the therapeutic potential of combined androgen blockade (CAB) with bicalutamide (Bic-CAB) as an initial treatment for metastatic hormone-sensitive prostate cancer (mHSPC) in Japan.
The electronic health records of 159 patients with mHSPC from three Japanese institutions who received initial treatment with Bic-CAB between 2007 and 2017 were analyzed. The time to prostate-specific antigen (PSA) progression, duration of Bic-CAB treatment, and overall survival (OS), with various definitions for PSA progression, were assessed. A multivariate Cox proportional hazards model was constructed using clinical parameters to predict time to the end of Bic-CAB treatment and OS.
The median observation period was 46.4 months, and the median age of patients at diagnosis was 71 years. A total of 46.5% patients experienced PSA progression with a median survival duration of 29 months (according to Prostate Cancer Clinical Trials Working Group 3 criteria), and 49.1% patients achieved a PSA nadir < 0.2 ng/mL in a median time of 4.7 months. When stratified by PSA nadir and PSA change, patients at low risk for disease progression with a small PSA change due to low initial PSA had a 5-year OS of 100% and a 10-year OS of 75%. The OS during the observation period was 72.9 months.
These findings highlight the potential effect of Bic-CAB in patients with mHSPC who were at low risk for disease progression. Initial treatment with Bic-CAB and adjusting treatment early based on PSA dynamics may be a reasonable treatment plan for these patients.
本回顾性观察性研究探讨了比卡鲁胺(Bic-CAB)联合雄激素阻断(CAB)作为初始治疗在日本转移性激素敏感性前列腺癌(mHSPC)的治疗潜力。
分析了 2007 年至 2017 年间在日本的三个机构接受初始 Bic-CAB 治疗的 159 例 mHSPC 患者的电子健康记录。评估了前列腺特异性抗原(PSA)进展时间、Bic-CAB 治疗持续时间和总生存(OS),并使用各种 PSA 进展定义。使用临床参数构建多变量 Cox 比例风险模型来预测 Bic-CAB 治疗结束时间和 OS。
中位观察期为 46.4 个月,诊断时患者的中位年龄为 71 岁。共有 46.5%的患者出现 PSA 进展,中位生存时间为 29 个月(根据前列腺癌临床试验工作组 3 标准),49.1%的患者在中位时间 4.7 个月内 PSA 达到<0.2ng/mL。根据 PSA 最低点和 PSA 变化进行分层,具有低疾病进展风险且由于初始 PSA 低而 PSA 变化较小的患者,5 年 OS 为 100%,10 年 OS 为 75%。在观察期间,OS 为 72.9 个月。
这些发现强调了 Bic-CAB 对疾病进展风险较低的 mHSPC 患者的潜在影响。对于这些患者,Bic-CAB 的初始治疗以及根据 PSA 动态调整治疗可能是一种合理的治疗方案。