Matsukawa Akihiro, Yanagisawa Takafumi, Parizi Mehdi Kardoust, Laukhtina Ekaterina, Klemm Jakob, Fazekas Tamás, Mori Keiichiro, Kimura Shoji, Briganti Alberto, Ploussard Guillaume, Karakiewicz Pierre I, Miki Jun, Kimura Takahiro, Rajwa Pawel, Shariat Shahrokh F
Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Urology, The Jikei University School of Medicine, Tokyo, Japan.
Prostate Cancer Prostatic Dis. 2024 Sep 5. doi: 10.1038/s41391-024-00886-0.
Androgen-receptor pathway inhibitors (ARPIs) have dramatically changed the management of advanced/metastatic prostate cancer (PCa). However, their cardiovascular toxicity remains to be clarified.
To analyze and compare the risks of cardiovascular events secondary to treatment of PCa patients with different ARPIs.
In August 2023, we queried PubMed, Scopus, and Web of Science databases to identify randomized controlled studies (RCTs) that analyze PCa patients treated with abiraterone, apalutamide, darolutamide, and enzalutamide. The primary outcomes of interest were the incidence of cardiac disorder, heart failure, ischemic heart disease (IHD), atrial fibrillation (AF), and hypertension. Network meta-analyses (NMAs) were conducted to compare the differential outcomes of each ARPI plus androgen deprivation therapy (ADT) compared to standard of care (SOC).
Overall, 26 RCTs were included. ARPIs were associated with an increased risk of cardiac disorders (RR: 1.74, 95% CI: 1.13-2.68, p = 0.01), heart failure (RR: 2.49, 95% CI: 1.05-5.91, p = 0.04), AF (RR: 2.15, 95% CI: 1.14-4.07, p = 0.02), and hypertension (RR: 2.06, 95% CI: 1.67-2.54, p < 0.01) at grade ≥3. Based on NMAs, abiraterone increased the risk of grade ≥3 cardiac disorder (RR:2.40, 95% CI: 1.42-4.06) and hypertension (RR:2.19, 95% CI: 1.77-2.70). Enzalutamide was associated with the increase of grade ≥3 AF(RR: 3.17, 95% CI: 1.05-9.58) and hypertension (RR:2.30, 95% CI: 1.82-2.92).
The addition of ARPIs to ADT increases the risk of cardiac disorders, including IHD and AF, as well as hypertension. Each ARPI exhibits a distinct cardiovascular event profile. Selecting patients carefully and vigilant monitoring for cardiovascular issues is imperative for those undergoing ARPI + ADT treatment.
雄激素受体通路抑制剂(ARPIs)极大地改变了晚期/转移性前列腺癌(PCa)的治疗方式。然而,它们的心血管毒性仍有待阐明。
分析和比较不同ARPIs治疗PCa患者继发心血管事件的风险。
2023年8月,我们检索了PubMed、Scopus和Web of Science数据库,以确定分析接受阿比特龙、阿帕他胺、达罗他胺和恩杂鲁胺治疗的PCa患者的随机对照研究(RCTs)。感兴趣的主要结局是心脏疾病、心力衰竭、缺血性心脏病(IHD)、心房颤动(AF)和高血压的发生率。进行网状荟萃分析(NMA)以比较每种ARPI联合雄激素剥夺治疗(ADT)与标准治疗(SOC)的不同结局。
总体而言,纳入了26项RCTs。ARPIs与≥3级心脏疾病(RR:1.74,95%CI:1.13 - 2.68,p = 0.01)、心力衰竭(RR:2.49,95%CI:1.05 - 5.91,p = 0.04)、AF(RR:2.15,95%CI:1.14 - 4.07,p = 0.02)和高血压(RR:2.06,95%CI:1.67 - 2.54,p < 0.01)的风险增加相关。基于NMA,阿比特龙增加了≥3级心脏疾病(RR:2.40,95%CI:1.42 - 4.06)和高血压(RR:2.19,95%CI:1.77 - 2.70)的风险。恩杂鲁胺与≥3级AF(RR:3.17,95%CI:1.05 - 9.58)和高血压(RR:2.30,95%CI:1.82 - 2.92)的增加相关。
在ADT基础上加用ARPIs会增加包括IHD和AF在内的心脏疾病以及高血压的风险。每种ARPI都表现出独特的心血管事件特征。对于接受ARPI + ADT治疗的患者,仔细选择患者并对心血管问题进行警惕监测至关重要。