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美国非转移性去势抵抗性前列腺癌患者的治疗模式和结局。

Treatment patterns and outcomes in patients with nonmetastatic castration-resistant prostate cancer in the United States.

机构信息

Huntsman Cancer Institute, University of Utah, Salt Lake City, UT USA.

Astellas Pharma Inc., Northbrook, IL USA.

出版信息

Future Oncol. 2024;20(32):2467-2480. doi: 10.1080/14796694.2024.2373681. Epub 2024 Jul 29.

Abstract

Androgen receptor pathway inhibitors (ARPIs) prolong metastasis-free survival and overall survival in patients with nonmetastatic castration-resistant prostate cancer (nmCRPC). This study aimed to evaluate real-world treatment patterns, utilization and survival outcomes in patients with nmCRPC. This retrospective cohort study used Optum database electronic health records of patients with nmCRPC from 1 January 2007 to 31 December 2020 in the US. Of 1955 patients, >80% received androgen-deprivation therapy (ADT) alone or ADT + first-generation nonsteroidal antiandrogen (NSAA) as first-line treatment, while only 8.24% received ADT + ARPI. ADT + ARPI remained underutilized even among those with high-risk nmCRPC. Further, ADT + NSAA had no survival benefit compared with ADT alone. Practice-improvement strategies are needed for treatment intensification with ARPIs for patients with nmCRPC.

摘要

雄激素受体通路抑制剂 (ARPIs) 可延长非转移性去势抵抗性前列腺癌 (nmCRPC) 患者的无转移生存期和总生存期。本研究旨在评估 nmCRPC 患者的真实世界治疗模式、应用情况和生存结局。这项回顾性队列研究使用了美国 Optum 数据库中 2007 年 1 月 1 日至 2020 年 12 月 31 日期间患有 nmCRPC 的患者的电子健康记录。在 1955 名患者中,>80%的患者接受了雄激素剥夺疗法 (ADT) 或 ADT+第一代非甾体类抗雄激素 (NSAA) 作为一线治疗,而仅有 8.24%的患者接受了 ADT+ARPI。即使在高危 nmCRPC 患者中,ARPI 的应用也仍然不足。此外,ADT+NSAA 与 ADT 单药治疗相比,并无生存获益。需要制定改善实践的策略,以加强对 nmCRPC 患者的 ARPI 治疗。

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