Abiraterone Followed by Enzalutamide Versus Enzalutamide Followed by Abiraterone in Chemotherapy-naive Patients With Metastatic Castration-resistant Prostate Cancer

恩扎鲁胺 医学 阿比曲酮 前列腺癌 肿瘤科 多西紫杉醇 化疗 醋酸阿比特龙酯 内科学 癌症 泌尿科 雄激素剥夺疗法 雄激素受体
作者
Nobuaki Matsubara,Yoko Yamada,Ken‐ichi Tabata,Takefumi Satoh,Naoto Kamiya,Hiroyoshi Suzuki,Takashi Kawahara,Hiroji Uemura,Akihiro Yano,Satoru Kawakami,Masafumi Otsuka,Satoshi Fukasawa
出处
期刊:Clinical Genitourinary Cancer [Elsevier BV]
卷期号:16 (2): 142-148 被引量:34
标识
DOI:10.1016/j.clgc.2017.09.008
摘要

Abstract Background Abiraterone (AA) and enzalutamide (ENZA) are increasingly being used in chemotherapy-naive patients with metastatic castration-resistant prostate cancer owing to efficacy and favorable toxicity. However, the order in which they should be administered has not been determined. Patients and Methods We retrospectively reviewed the records of chemotherapy-naive patients with metastatic castration-resistant prostate cancer who had received sequential treatment with either AA followed by ENZA (AA-ENZA) or the converse (ENZA-AA). Prostate-specific antigen (PSA) response rates (defined as ≥ 50% PSA decline from baseline), first-line progression-free survival (PFS), second-line PFS, combined PFS (defined as first-line PFS plus second-line PFS), and overall survival are compared between the 2 sequence groups. Results A total of 97 patients received sequential treatment with AA and ENZA; 50 patients were in the AA-ENZA group, and 47 patients were in the ENZA-AA group. The PSA response rate to first-line treatment was not significantly different between AA (48%) and ENZA (51%) ( P  = .840). However, a significant difference was observed in the PSA response rate to second-line treatment (AA, 6.4% vs. ENZA, 30%; P  = .004). The median combined PFS was not significantly different between sequence groups (hazard ratio, 0.71; 95% confidence interval, 0.46-1.08; log-rank P  = .105). The order of addition also had no significant effect on median overall survival (hazard ratio, 0.98; 95% confidence interval, 0.64-1.52; log-rank P  = .834). Conclusion With the exception of the second-line PSA response, there was no significant difference in clinical outcomes between the AA-ENZA and ENZA-AA groups. Our results might be useful reference in daily practice, especially for patients who do not have a suitable general condition for chemotherapy.
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