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Real-world Comparative Study of Androgen Receptor Signaling Inhibitors in Japanese Patients With Non-metastatic Castration-resistant Prostate Cancer

医学 中止 耐受性 恩扎鲁胺 不利影响 前列腺癌 内科学 肿瘤科 雄激素受体 毒性 队列 回顾性队列研究 癌症 前列腺特异性抗原 抗雄激素 危险系数 病历 临床试验 队列研究 联合疗法 癌症登记处 比卡鲁胺 不良事件通用术语标准 入射(几何) 放射治疗 雄激素剥夺疗法 化疗
作者
Masaaki Yanishi,Seiji Shimada,Takao Mishima,HIDEFUMI KINOSHITA
出处
期刊:Anticancer Research [International Institute of Anticancer Research (IIAR) Conferences 1997. Athens, Greece. Abstracts]
卷期号:46 (4): 2145-2151
标识
DOI:10.21873/anticanres.18103
摘要

BACKGROUND/AIM: Androgen receptor signaling inhibitors (ARSIs) are widely used for non-metastatic castration-resistant prostate cancer (nmCRPC). However, real-world data comparing clinical outcomes and treatment persistence among ARSIs in Asian populations remain limited. This study aimed to evaluate real-world effectiveness and tolerability of ARSIs in Japanese patients with nmCRPC. PATIENTS AND METHODS: We retrospectively reviewed 100 Japanese patients with nmCRPC treated with enzalutamide (ENZ), apalutamide (APA), or darolutamide (DARO) at Kansai Medical University and its affiliated hospitals between May 2020 and December 2024. Progression-free survival (PFS), overall survival (OS), prostate-specific antigen (PSA) response, treatment sequencing, and adverse event-related dose modification or discontinuation were analyzed using Kaplan-Meier and log-rank tests. RESULTS: =0.03), while DARO demonstrated comparable outcomes to both agents. OS did not differ significantly among groups. Patients receiving ARSI as first-line therapy had significantly longer PFS than those treated with second-line ARSIs. Initiation of ARSI therapy at PSA levels <2.0 ng/ml was associated with improved PFS. Second-line ARSI therapy showed limited PSA response and shorter PFS. Adverse event-related dose reduction or treatment discontinuation was associated with poorer PFS, with dermatologic toxicity being the main cause of APA discontinuation. CONCLUSION: In Japanese real-world practice, ARSI effectiveness in nmCRPC appears influenced by treatment persistence, timing of initiation, and treatment sequencing. Early initiation and careful management of adverse events may optimize outcomes, whereas sequential ARSI use shows limited benefit.
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