Cardio-Oncology Center of Excellence, Division of Cardiology, University of Pennsylvania, Philadelphia, PA.
Cardio-Oncology Program, Division of Cardiology, University of South Florida and Moffitt Cancer Center.
J Immunother. 2021;44(2):86-89. doi: 10.1097/CJI.0000000000000341.
Adoptive cellular therapy (ACT) with tumor-infiltrating lymphocytes (TILs) has emerged as an effective treatment option for unresectable stage III/IV metastatic melanoma. Acute toxicities, particularly cardiovascular (CV), can have a significant effect on the completion of therapy. We abstracted information on 43 patients who received ACT-TIL treatment for melanoma at the Moffitt Cancer Center between 2010 and 2016. The Student t tests and χ2 tests were used to compare patient characteristics by presence versus absence of specific CV complications. In this cohort, 32.6% developed hypotension requiring treatment with intravenous fluids and pressors, 14% atrial fibrillation, and 2.3% troponin elevations suggestive of myocardial damage. No patients developed clinical heart failure, and among the patients that underwent echocardiography, there was no significant difference in mean left ventricular ejection fraction before or after therapy (62.9% vs. 63.5%, respectively, P=0.79). There was also no statistically significant difference in survival between those with and without CV complications (overall survival=61.9%, mean: 26.0 mo and progression-free survival=45.2%, mean: 18.1 mo). CV toxicities are common in ACT-TIL protocols; however, survival does not appear to be significantly affected. Further research is needed to define mechanisms and potential prevention strategies to help clinicians manage these complications and mitigate risk.
过继性细胞疗法(ACT)联合肿瘤浸润淋巴细胞(TIL)已成为治疗不可切除的 III/IV 期转移性黑色素瘤的有效方法。急性毒性,尤其是心血管毒性(CV),会对治疗的完成产生重大影响。我们分析了 2010 年至 2016 年间莫菲特癌症中心接受 ACT-TIL 治疗黑色素瘤的 43 名患者的信息。采用 Student t 检验和 χ2 检验比较了 CV 并发症存在与否时患者特征的差异。在该队列中,32.6%的患者发生低血压,需要静脉补液和升压药治疗;14%的患者发生心房颤动;2.3%的患者肌钙蛋白升高提示心肌损伤。没有患者发生临床心力衰竭;在接受超声心动图检查的患者中,治疗前后左心室射血分数无显著差异(分别为 62.9%和 63.5%,P=0.79)。有 CV 并发症和无 CV 并发症的患者的生存也无统计学差异(总生存=61.9%,平均:26.0 个月;无进展生存=45.2%,平均:18.1 个月)。CV 毒性在 ACT-TIL 方案中很常见;然而,生存似乎没有受到显著影响。需要进一步研究以确定机制和潜在的预防策略,以帮助临床医生管理这些并发症并降低风险。