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Related Concept Videos

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Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
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Cardiotoxic Effects Following CAR-T Cell Therapy: A Literature Review.

Tony Joseph1,2, Jimmy Sanchez1, Ahmed Abbasi3

  • 1Department of Radiology, Albert Einstein College of Medicine and the Montefiore Medical Center, 111 East 210Th Street, Bronx, NY, 10461, USA.

Current Oncology Reports
|January 21, 2025
PubMed
Summary
This summary is machine-generated.

Chimeric Antigen Receptor T-cell (CAR-T) therapy, while effective for blood cancers, poses significant risks of cardiotoxicity. Patients with severe cytokine release syndrome (CRS) face higher cardiac event risks, necessitating further long-term studies.

Keywords:
Atrial arrhythmiaBlood biomarkersCancer immunotherapyCardiomyopathyCardiotoxicityCytokine release syndrome (CRS)Diastolic dysfunctionECGEKGEchocardiogramHypotensionTroponin (TNT)

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Area of Science:

  • Oncology
  • Cardiology
  • Immunotherapy

Background:

  • Chimeric Antigen Receptor T-cell (CAR-T) therapy is a revolutionary treatment for hematological malignancies.
  • CAR-T therapy is associated with significant side effects, notably cardiotoxicity.

Purpose of the Study:

  • To review the current literature on the incidence, clinical manifestations, and risk factors of CAR-T therapy-associated cardiotoxicity.
  • To synthesize findings from limited and heterogeneous studies on CAR-T cardiotoxicity.

Main Methods:

  • Literature review of published studies on CAR-T cardiotoxicity.
  • Analysis of clinical manifestations, incidence, and risk factors.
  • Examination of cardiac events and echocardiographic findings.

Main Results:

  • CAR-T therapy is linked to substantial risks of acute and subacute cardiotoxicity.
  • Higher-grade cytokine release syndrome (CRS) (grade 2 or higher) is associated with increased cardiotoxicity risk.
  • Common cardiac events include hypotension, tachycardia, heart failure, arrhythmias, and cardiomyopathy; echocardiographic changes involve systolic and diastolic dysfunction.

Conclusions:

  • CAR-T cardiotoxicity is a significant concern requiring careful monitoring.
  • Differences in cardiotoxicity exist between adult and pediatric populations.
  • Long-term effects of CAR-T therapy on the heart remain largely unknown, warranting further investigation.