Lowentritt Benjamin, Bilen Mehmet A, Khilfeh Ibrahim, Rossi Carmine, Du Shawn, Kinkead Frederic, Diaz Lilian, Pilon Dominic, Ellis Lorie, Shore Neal D
Chesapeake Urology, Towson, MD 21204, USA.
Winship Cancer Institute of Emory University, Atlanta, GA 30322, USA.
J Comp Eff Res. 2025 Jul;14(7):e250023. doi: 10.57264/cer-2025-0023. Epub 2025 May 9.
Head-to-head studies of survival outcomes associated with different androgen receptor pathway inhibitor (ARPI) treatments for metastatic castration (hormone)-sensitive prostate cancer have not been conducted. The purpose of this study was to compare 24-month overall survival among ARPI-naive patients with metastatic castration-sensitive prostate cancer (mCSPC) who initiated apalutamide or abiraterone acetate. Linked de-identified clinical and claims healthcare databases were used to compare overall survival between patients with mCSPC initiating apalutamide or abiraterone acetate treated in community-based urology practices in the USA. Overall survival at 24 months post-treatment initiation (primary analyses) was compared between apalutamide and abiraterone acetate initiators using weighted Cox proportional hazards models (exploratory analyses used all available follow-up). Overall, 1879 and 2073 patients had initiated apalutamide or abiraterone acetate, respectively (both cohorts: weighted mean age 72 years, 62% were white, and 66% had bone metastasis). At 24 months post-index, patients in the apalutamide cohort had a 26% lower risk of mortality compared with those in the abiraterone acetate cohort (hazard ratio: 0.74; 95% confidence interval: 0.59, 0.93; p = 0.010), with the difference maintained when outcomes were evaluated using all available follow-up (hazard ratio: 0.72; 95% confidence interval: 0.59, 0.88; nominal p < 0.001). In this nationally representative, real-world head-to-head analysis of nearly 4000 ARPI-naive patients with mCSPC, apalutamide was associated with a 26% reduction in the risk of mortality compared with abiraterone acetate by 24 months post-treatment initiation.
尚未开展针对转移性去势(激素)敏感性前列腺癌的不同雄激素受体通路抑制剂(ARPI)治疗的生存结局的头对头研究。本研究的目的是比较开始使用阿帕他胺或醋酸阿比特龙的初治ARPI的转移性去势敏感性前列腺癌(mCSPC)患者的24个月总生存率。利用去识别化的临床和医保理赔医疗数据库,比较在美国社区泌尿外科诊所接受阿帕他胺或醋酸阿比特龙治疗的mCSPC患者的总生存率。使用加权Cox比例风险模型比较阿帕他胺和醋酸阿比特龙起始治疗者治疗开始后24个月的总生存率(探索性分析使用所有可用的随访数据)。总体而言,分别有1879例和2073例患者开始使用阿帕他胺或醋酸阿比特龙(两个队列:加权平均年龄72岁,62%为白人,66%有骨转移)。在索引日期后24个月,阿帕他胺队列患者的死亡风险比醋酸阿比特龙队列患者低26%(风险比:0.74;95%置信区间:0.59,0.93;p = 0.010),当使用所有可用随访数据评估结局时,该差异依然存在(风险比:0.72;95%置信区间:0.59,0.88;名义p < 0.001)。在这项对近4000例初治ARPI的mCSPC患者进行的具有全国代表性的真实世界头对头分析中,与醋酸阿比特龙相比,阿帕他胺在治疗开始后24个月时可使死亡风险降低26%。