评估用于治疗前列腺癌的新一代雄激素受体通路抑制剂引发的心血管事件:日本真实世界研究

IF 2.5 3区 医学 Q3 ONCOLOGY Oncology Pub Date : 2024-08-14 DOI:10.1159/000540864
Rikuto Masuda, Yoshihiro Noguchi, Haruka Aizawa, Shunsuke Yoshizawa, Yuki Nomura, Mitsuru Saguchi, Kazuhiro Iguchi, Tomoaki Yoshimura
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引用次数: 0

摘要

导言:能显著改善前列腺癌患者预后的雄激素受体通路抑制剂(ARPI)包括醋酸阿比特龙(雄激素合成抑制剂)和恩扎鲁胺(雄激素受体抑制剂)。最近有报告称,利用美国食品药品管理局(FDA)不良事件报告系统(FAERS)对ARPI和心血管事件进行了分析;然而,有关醋酸阿比特龙和恩杂鲁胺在实际临床实践中的心血管事件的证据还不充分。本研究利用日本的大型医疗机构数据库--日本医疗数据中心(JMDC)医疗机构数据库(JMDC Inc.,日本东京),检验了恩杂鲁胺的心血管事件风险低于醋酸阿比特龙的假设:利用JMDC医疗机构数据库,纳入2014年10月至2022年2月期间新使用醋酸阿比特龙或恩杂鲁胺且未发生重大心血管事件的患者。使用倾向得分匹配法调整年龄、合并症和伴随用药后,比较了作为主要终点的心血管死亡和所有心血管事件的累积发病率,以及作为次要终点的主要心血管事件、心肌梗死、心力衰竭和中风的累积发病率:恩杂鲁胺组共有3033名患者,阿比特龙组共有2021名患者符合资格标准。经过倾向评分匹配后,恩杂鲁胺组有1940名患者,阿比特龙组有1940名患者。与阿比特龙相比,恩杂鲁胺的心血管死亡累积率(危险比[HR]:0.30,95%置信区间[CI]:0.10-0.93)、所有心血管事件(HR:0.79,95% CI:0.64-0.98)、主要心血管事件(HR:0.79,95% CI:0.64-0.97)和心肌梗死(HR:0.62,95% CI:0.46-0.84)均显著降低:结论:在全国男性前列腺癌患者样本中,新接受恩杂鲁胺治疗的患者发生不良心血管事件的风险低于接受醋酸阿比特龙治疗的患者。
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Assessment of Cardiovascular Events Caused by New-Generation Androgen Receptor Pathway Inhibitors Used for Prostate Cancer: A Real-World Study in Japan.

Introduction: Androgen receptor pathway inhibitors (ARPIs) that significantly improve the prognosis of patients with prostate cancer include abiraterone acetate (androgen synthesis inhibitor) and enzalutamide (androgen receptor inhibitor). A recent analysis of ARPI and cardiovascular events using the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) has been reported; however, the evidence on cardiovascular events for abiraterone acetate and enzalutamide in real-world clinical practice is insufficient. Using a large Japanese database of medical institutions, the Japanese Medical Data Center (JMDC) medical institution database (JMDC Inc., Tokyo, Japan), this study tested the hypothesis that the risk of cardiovascular events with enzalutamide is lower than that with abiraterone acetate.

Method: Using the JMDC medical institution database, patients with new use of abiraterone acetate or enzalutamide who had not experienced a major cardiovascular event between October 2014 and February 2022 were included. After adjusting for age, comorbidities, and concomitant medications using propensity score matching, cumulative incidence rates were compared for cardiovascular death and all cardiovascular events as the primary endpoints, and major cardiovascular events, myocardial infarction, heart failure, and stroke as secondary endpoints.

Result: A total of 3,033 patients in the enzalutamide group and 2,021 in the abiraterone group met the eligibility criteria. After propensity score matching, the cohort included 1,940 patients in the enzalutamide group and 1,940 patients in the abiraterone group. Enzalutamide was associated with significantly lower cumulative rates of cardiovascular death (hazard ratio [HR]: 0.30, 95% confidence interval [CI]: 0.10-0.93), all cardiovascular events (HR: 0.79, 95% CI: 0.64-0.98), major cardiovascular events (HR: 0.79, 95% CI: 0.64-0.97), and myocardial infarction (HR: 0.62, 95% CI: 0.46-0.84) compared to abiraterone.

Conclusion: In a national sample of males with prostate cancer, those newly treated with enzalutamide had a lower risk of adverse cardiovascular events than those treated with abiraterone acetate.

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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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