Doran Stacey, Mysore Manu, Kassaian Seyed Ebrahim, Kotloff Ethan, Kamangar Farin, Emadi Ashkan, Apata Jummai, Barr Brian
National Cancer Institute, Bethesda, MD, United States.
Department of Medicine, Division of Cardiovascular Medicine, University of Maryland School of Medicine, Baltimore, MD, United States.
Front Cardiovasc Med. 2023 Jun 8;10:1129943. doi: 10.3389/fcvm.2023.1129943. eCollection 2023.
Use of the proteasome inhibitor carfilzomib has become a standard of care in patients with relapsed/refractory multiple myeloma. An association between carfilzomib and cardiovascular adverse events has been well documented, but this had not been investigated in a racially diverse population. Black patients in particular are underrepresented in the reported outcomes of treatment with carfilzomib.
The purpose of this study was to identify risk factors for carfilzomib-associated cardiovascular events in a diverse, single-center population.
We conducted a retrospective review of 161 patients with multiple myeloma treated with carfilzomib between 2011 and 2020 at the University of Maryland Medical Center. Over half (86) were Black patients, with the remainder (75) being White patients. We did a multivariate analysis to determine risk factors for developing cardiovascular events during treatment with carfilzomib.
There was no statistically significant association with cardiotoxicity and race, gender, or age at first dose of carfilzomib. In multivariable analysis, patients with history of hypertension had a higher risk of cardiotoxicity [adjusted odds ratio (OR): 2.5; 95% CI: 1.1-5.9; = 0.03] as did those with a history of smoking [OR: 2.8; 95% CI: 1.3-6.4; = 0.01].
Here we report the largest cohort of Black patients treated with carfilzomib as yet reported. The results of this single center retrospective study show history of hypertension and smoking are associated with carfilzomib associated cardiotoxicity in a diverse patient population. There is a need for well-designed prospective studies enrolling a diverse population to investigate potential interventions to prevent carfilzomib-associated cardiotoxicity.
蛋白酶体抑制剂卡非佐米已成为复发/难治性多发性骨髓瘤患者的标准治疗药物。卡非佐米与心血管不良事件之间的关联已有充分记录,但尚未在种族多样化人群中进行研究。特别是黑人患者在卡非佐米治疗的报告结果中代表性不足。
本研究的目的是在一个多样化的单中心人群中确定与卡非佐米相关的心血管事件的危险因素。
我们对2011年至2020年在马里兰大学医学中心接受卡非佐米治疗的161例多发性骨髓瘤患者进行了回顾性研究。超过一半(86例)为黑人患者,其余(75例)为白人患者。我们进行了多变量分析,以确定卡非佐米治疗期间发生心血管事件的危险因素。
在首次使用卡非佐米时,心脏毒性与种族、性别或年龄之间无统计学显著关联。在多变量分析中,有高血压病史的患者发生心脏毒性的风险更高[调整后的优势比(OR):2.5;95%置信区间:1.1-5.9;P = 0.03],有吸烟史的患者也是如此[OR:2.8;95%置信区间:1.3-6.4;P = 0.01]。
我们报告了迄今为止接受卡非佐米治疗的最大规模黑人患者队列。这项单中心回顾性研究的结果表明,在多样化的患者群体中,高血压病史和吸烟史与卡非佐米相关的心脏毒性有关。需要开展设计良好的前瞻性研究,纳入多样化人群,以调查预防卡非佐米相关心脏毒性的潜在干预措施。