MINI REVIEW article

Front. Pharmacol.

Sec. Cardiovascular and Smooth Muscle Pharmacology

Volume 16 - 2025 | doi: 10.3389/fphar.2025.1578157

This article is part of the Research TopicTargets in Cardio-Oncology: Drug Effects and Mechanisms of ActionView all 13 articles

Cardiovascular Toxicities Associated with Chimeric Antigen Receptor T Cell Therapy

Provisionally accepted
  • 1Cancer Research Institute of Jilin University, The First Hospital of Jilin University, Changchun, China
  • 2Department of Pharmacy, China-Japan Union Hospital, Jilin University, Changchun, Hebei Province, China

The final, formatted version of the article will be published soon.

Chimeric antigen receptor (CAR) T cell therapy has emerged as a groundbreaking immunotherapeutic approach, particularly for oncohematological patients who are refractory to conventional treatments. As clinical trials expand the applications of CAR T therapy beyond hematologic malignancies, a critical understanding of its associated toxicities, particularly cardiovascular complications, becomes imperative. This review synthesizes current literature on the interplay between cytokine release syndrome (CRS) and cardiotoxicity related to CAR T therapy, emphasizing the potential severity of these adverse events. While significant progress has been made in managing CRS, the cardiac manifestations-ranging from mild events to life-threatening complications-remain underreported in pivotal studies. We explore the incidence and nature of cardiotoxicity in real-world and clinical trial settings, identify risk factors contributing to cardiovascular events, and propose guidelines for pretherapy evaluations, post-infusion monitoring, and management strategies. By highlighting the urgent need for heightened awareness and proactive care, this review aims to enhance patient safety and optimize outcomes in the evolving landscape of CAR T therapy.

Keywords: CAR T cell, Cardio-oncology, cytokine release syndrome, cardiotoxicity, Chimeric Antigen Receptor

Received: 17 Feb 2025; Accepted: 08 Apr 2025.

Copyright: © 2025 Zhou, Liu, Liu, Zhao and Jiang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Xin Zhou, Cancer Research Institute of Jilin University, The First Hospital of Jilin University, Changchun, China

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