Sayer Michael, Hamano Hirofumi, Nagasaka Misako, Lee Benjamin J, Doh Jean, Patel Pranav M, Zamami Yoshito, Ozaki Aya F
School of Pharmacy & Pharmaceutical Sciences, University of California, 802 W Peltason Dr, Room 106A, Irvine, CA, 92617, USA.
Department of Pharmacy, Okayama University Hospital, Okayama, Japan.
Cardiooncology. 2025 Apr 28;11(1):40. doi: 10.1186/s40959-025-00331-8.
Cardio-inflammatory immune related adverse events (irAEs) while receiving immune checkpoint inhibitor (ICI) therapy are particularly consequential due to their associations with poorer treatment outcomes. Evaluation of predictive factors of these serious irAEs with a time dependent approach allows better understanding of patients most at risk.
To identify different elements of patient data that are significant predictors of early and late-onset or delayed cardio-inflammatory irAEs through various predictive modeling strategies.
A cohort of patients receiving ICI therapy from January 1, 2010 to May 1, 2022 was identified from TriNetX meeting inclusion/exclusion criteria. Patient data collected included occurrence of early and later cardio-inflammatory irAEs, patient survival time, patient demographic information, ICI therapies, comorbidities, and medication histories. Predictive and statistical modeling approaches identified unique risk factors for early and later developing cardio-inflammatory irAEs.
A cohort of 66,068 patients on ICI therapy were identified in the TriNetX platform; 193 (0.30%) experienced early cardio-inflammatory irAEs and 175 (0.26%) experienced later cardio-inflammatory irAEs. Significant predictors for early irAEs included: anti-PD-1 therapy at index, combination ICI therapy at index, and history of peripheral vascular disease. Significant predictors for later irAEs included: a history of myocarditis and/or pericarditis, cerebrovascular disease, and history of non-steroidal anti-inflammatory medication use.
Cardio-inflammatory irAEs can be divided into clinically meaningful categories of early and late based on time since initiation of ICI therapy. Considering distinct risk factors for early-onset and late-onset events may allow for more effective patient monitoring and risk assessment.
接受免疫检查点抑制剂(ICI)治疗时发生的心脏炎症性免疫相关不良事件(irAEs)因其与较差的治疗结果相关,故而尤为重要。采用时间依赖性方法评估这些严重irAEs的预测因素,有助于更好地了解风险最高的患者。
通过各种预测建模策略,确定患者数据中不同因素,这些因素是早期和迟发性或延迟性心脏炎症性irAEs的重要预测指标。
根据TriNetX会议纳入/排除标准,确定一组在2010年1月1日至2022年5月1日期间接受ICI治疗的患者。收集的患者数据包括早期和晚期心脏炎症性irAEs的发生情况、患者生存时间、患者人口统计学信息、ICI治疗、合并症和用药史。预测和统计建模方法确定了早期和晚期发生心脏炎症性irAEs的独特风险因素。
在TriNetX平台上确定了一组66,068例接受ICI治疗的患者;193例(0.30%)发生早期心脏炎症性irAEs,175例(0.26%)发生晚期心脏炎症性irAEs。早期irAEs的重要预测因素包括:首次使用抗PD-1治疗、首次使用联合ICI治疗以及外周血管疾病史。晚期irAEs的重要预测因素包括:心肌炎和/或心包炎病史、脑血管疾病以及使用非甾体抗炎药的病史。
根据ICI治疗开始后的时间,心脏炎症性irAEs可分为具有临床意义的早期和晚期类别。考虑早发性和迟发性事件的不同风险因素,可能有助于更有效地对患者进行监测和风险评估。