School of Chemical Engineering, Ocean and Life Sciences, Dalian University of Technology, Panjin, China.
Br J Clin Pharmacol. 2024 Sep;90(9):2067-2078. doi: 10.1111/bcp.16176. Epub 2024 Jul 11.
Androgen receptor inhibitors (ARIs) have become an effective treatment for advanced prostate cancer (PC). However, it is unknown which ARI is the most helpful and safe for men with advanced PC. Our aim is to help physicians make clinical decisions and provide medication guidelines for patients with advanced PC to avoid potential risks when using ARIs for treatment.
We systematically searched the following databases: PubMed, Embase and Cochrane Library, with a literature publication deadline of February 2023. The primary efficacy outcomes were 18-month overall survival (OS), treatment-emergent adverse events (TEAEs), hypertension and fatigue. The network meta-analysis (NMA) was performed by Stata 15.1, and Revman 5.3 was used to assess the included studies' risk of bias.
The analysis included 26 trials with 26 263 people. The surface under the cumulative ranking curve (SUCRA) concluded that enzalutamide (86.8%) showed the best effect in prolonging the OS of patients. Flutamide led to the highest risk of TEAEs (29.9%) and AEs leading to discontinuation (12.8%). Apalutamide (13.4%) led to the highest risk of grade ≥3 TEAEs. Enzalutamide had the highest risk of hypertension (0.2%), grade ≥3 hypertension (4.5%) and fatigue (5.2%).
This NMA indicates there is no one ARI to reach both the most effective and safe therapy aims for treating advanced PC and that there is a compromise between the efficacy and safety of ARIs in the treatment of advanced PC. Physicians should weigh the risks to safety against the anticipated benefits when prescribing these drugs to patients with PC.
雄激素受体抑制剂(ARIs)已成为治疗晚期前列腺癌(PC)的有效方法。然而,尚不清楚哪种 ARI 对晚期 PC 患者最有帮助和最安全。我们的目的是帮助医生做出临床决策,并为晚期 PC 患者提供用药指南,以避免在使用 ARIs 治疗时出现潜在风险。
我们系统地检索了以下数据库:PubMed、Embase 和 Cochrane Library,文献发表截止日期为 2023 年 2 月。主要疗效结局为 18 个月总生存(OS)、治疗后出现的不良事件(TEAEs)、高血压和疲劳。网络荟萃分析(NMA)由 Stata 15.1 进行,Revman 5.3 用于评估纳入研究的偏倚风险。
分析纳入了 26 项试验,共 26263 人。累积排序曲线下面积(SUCRA)的结论是,恩扎卢胺(86.8%)在延长患者 OS 方面效果最好。氟他胺导致 TEAEs(29.9%)和因不良反应而停药(12.8%)的风险最高。阿帕鲁胺(13.4%)导致≥3 级 TEAEs 的风险最高。恩扎卢胺导致高血压(0.2%)、≥3 级高血压(4.5%)和疲劳(5.2%)的风险最高。
这项 NMA 表明,没有一种 ARI 能够同时达到治疗晚期 PC 最有效和最安全的治疗目标,在治疗晚期 PC 时,ARIs 的疗效和安全性之间存在权衡。医生在为 PC 患者开具这些药物时,应权衡安全性风险与预期获益。