Joseph Luke, C Nickel Andrew, Patel Akshar, F Saba Nabil, R Leon Angel, F El-Chami Mikhael, M Merchant Faisal
Emory University School of Medicine, Atlanta, GA.
University of Colorado School of Medicine, Aurora, CO.
J Atr Fibrillation. 2021 Feb 28;13(5):2461. doi: 10.4022/jafib.2461. eCollection 2021 Feb-Mar.
Cancer treatmentinduced arrhythmia (CTIA) is a well-recognized form of cardiotoxicity associated with chemotherapy. Immune checkpoint inhibitors (ICI) have been associated with important forms of cardiotoxicity, including myocarditis. However, the incidence of CTIA associated with ICI has not been well characterized.
We reviewed all patients treated with ICIs at our institution from Jan. 2010 to Oct. 2015. CTIA was defined as a new diagnosis of clinically relevant arrhythmia within 6 months after ICI initiation.
During the study period, 268 patients were treated with immune checkpoint inhibitors, of whom 190 received monotherapy with ipilimumab (n=114), nivolumab (n=52) or pembrolizumab (n=24) and 78 received combination therapy: ipilimumab & nivolumab (n=37), ipilimumab & pembrolizumab (n=39) and nivolumab & pembrolizumab (n=2). Four patients (1.5%) developed CTIA. Of these, 3 patients developed a new diagnosis of atrial fibrillation (AF), one of whom required cardioversion. In 2 cases of new-onset AF, significant provoking factors were present in addition to ICI therapy including thyrotoxicosis in one and metabolic disarray in another. Six patients (2.2%) with a pre-existing diagnosis of paroxysmal AF experienced episodes within 6 months of initiating ICI therapy. None of the arrhythmic events were associated with known or suspected myocarditis.
The incidence of arrhythmic complications associated with immune checkpoint inhibitors appears to be very low (~1.5%). Patients with a pre-existing diagnosis of AF may be at-risk of recurrence during ICI treatment and should be monitored accordingly. These suggest that from an arrhythmia perspective, ICIs appear to be very safe and well-tolerated.
癌症治疗诱发的心律失常(CTIA)是一种与化疗相关的公认的心脏毒性形式。免疫检查点抑制剂(ICI)已与包括心肌炎在内的重要心脏毒性形式相关联。然而,与ICI相关的CTIA的发生率尚未得到很好的描述。
我们回顾了2010年1月至2015年10月在我们机构接受ICI治疗的所有患者。CTIA被定义为在ICI开始后6个月内新诊断出的临床相关心律失常。
在研究期间,268例患者接受了免疫检查点抑制剂治疗,其中190例接受了伊匹单抗(n = 114)、纳武单抗(n = 52)或派姆单抗(n = 24)的单药治疗,78例接受了联合治疗:伊匹单抗与纳武单抗(n = 37)、伊匹单抗与派姆单抗(n = 39)以及纳武单抗与派姆单抗(n = 2)。4例患者(1.5%)发生了CTIA。其中,3例患者新诊断出房颤(AF),其中1例需要进行心脏复律。在2例新发房颤病例中,除ICI治疗外还存在重要的诱发因素,其中1例为甲状腺毒症,另1例为代谢紊乱。6例既往诊断为阵发性房颤的患者在开始ICI治疗后6个月内出现发作。心律失常事件均与已知或疑似心肌炎无关。
与免疫检查点抑制剂相关的心律失常并发症的发生率似乎非常低(约1.5%)。既往诊断为房颤的患者在ICI治疗期间可能有复发风险,应相应进行监测。这些表明,从心律失常的角度来看,ICI似乎非常安全且耐受性良好。