J Pharm Pharm Sci. 2020;23:451-461. doi: 10.18433/jpps31003.
To compare the effectiveness and safety between abiraterone and enzalutamide in the treatment of patients with metastatic castration-resistant prostate cancer (mCRPC).
We systematically searched for relevant articles from PubMed, Cochrane, Embase from their inception through November 4, 2019. Available articles from conferences were searched. The endpoints were prostate-specific antigen (PSA) response, overall survival (OS), progression-free survival (PFS), number of patients with any adverse event (AE).
15 cohort studies involving 3546 participants were included in this meta-analysis. Pooled result showed that PSA response rate in the enzalutamide group was significantly greater than that in the abiraterone group (867 patients, risk ratio (RR) 0.69, 95% confidence interval (CI) 0.61-0.79, p<0.00001, I2=29%). There was no significant difference in the total incidence of AEs between two groups (730 patients, RR 0.42, 95% CI 0.14-1.31, p = 0.14, I2=84%). The common adverse events observed in the published articles were fatigue and perceived cognitive impairments. Patients who received enzalutamide had the higher risk to have the feeling of fatigue compared with abiraterone group (2555 patients, RR 0.45, 95% CI 0.24-0.85, p=0.01, I2=92%). And there was no statistical difference between two groups respect to the side effect of perceived cognitive impairments (1856 patients, RR 0.94, 95% CI 0.47-1.88, p=0.85, I2=15%).
Our results demonstrated that enzalutamide was associated with higher PSA response rate compared to abiraterone in patients with mCRPC, and no significant difference was found between two groups in the overall AE. But enzalutamide use induced higher risk of the AE of fatigue.
比较阿比特龙和恩扎鲁胺在治疗转移性去势抵抗性前列腺癌(mCRPC)患者中的疗效和安全性。
我们系统地从 PubMed、Cochrane、Embase 数据库建库至 2019 年 11 月 4 日进行文献检索,并检索会议相关文献。结局指标包括前列腺特异抗原(PSA)反应率、总生存期(OS)、无进展生存期(PFS)和任何不良事件(AE)的患者人数。
纳入的 15 项队列研究共包含 3546 例患者。汇总结果显示,恩扎鲁胺组 PSA 反应率显著高于阿比特龙组(867 例患者,风险比(RR)0.69,95%置信区间(CI)0.61-0.79,p<0.00001,I²=29%)。两组的总不良反应发生率无显著差异(730 例患者,RR 0.42,95%CI 0.14-1.31,p=0.14,I²=84%)。已发表文章中观察到的常见不良反应为疲劳和认知功能障碍。与阿比特龙组相比,接受恩扎鲁胺治疗的患者出现疲劳的风险更高(2555 例患者,RR 0.45,95%CI 0.24-0.85,p=0.01,I²=92%)。两组在认知功能障碍的不良反应方面无统计学差异(1856 例患者,RR 0.94,95%CI 0.47-1.88,p=0.85,I²=15%)。
本研究结果表明,与阿比特龙相比,恩扎鲁胺治疗 mCRPC 患者的 PSA 反应率更高,两组的总体不良反应无显著差异。但恩扎鲁胺治疗可增加疲劳不良反应的发生风险。