Cited by 138Chemotherapy-induced cardiotoxicity and mitigationCancer Immunotherapy and BiomarkersAtherosclerosis and Cardiovascular Diseases

Mechanisms of Cardiovascular Toxicities Associated With Immunotherapies

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Baik, Alan H., Oluwole, Olalekan O., Johnson, Douglas B., Shah, Nina, Salem, Joe-Elie, Tsai, Katy K., Moslehi, Javid J.·2021·Circulation Research

Abstract

Immune-based therapies have revolutionized cancer treatments. Cardiovascular sequelae from these treatments, however, have emerged as critical complications, representing new challenges in cardio-oncology. Immune therapies include a broad range of novel drugs, from antibodies and other biologics, including immune checkpoint inhibitors and bispecific T-cell engagers, to cell-based therapies, such as chimeric-antigen receptor T-cell therapies. The recognition of immunotherapy-associated cardiovascular side effects has also catapulted new research questions revolving around the interactions between the immune and cardiovascular systems, and the signaling cascades affected by T cell activation, cytokine release, and immune system dysregulation. Here, we review the specific mechanisms of immune activation from immunotherapies and the resulting cardiovascular toxicities associated with immune activation and excess cytokine production.

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Crossref · 10.1161/circresaha.120.315894

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  • ICI myocarditis has a fatality rate of up to 50%.

    “ICI myocarditis has a high fatality rate of up to 50%.”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [180]

    The Immune Checkpoint Inhibitors section describes ICI-associated myocarditis as having a high fatality rate, but gives the rate as 39.7%, not up to 50%. The cited review supports the severity of the claim but not its stated figure. (LLM, conf=0.87)

    Experimental — accuracy not yet measured
  • ICI myocarditis occurs in less than 1% of patients.

    “Despite occurring in <1% of patients”

    From Autoimmune Myocarditis, Old Dogs and New Tricks. (2024) · cites this paper as [180]

    The Immune Checkpoint Inhibitors section describes ICI-associated myocarditis as occurring about 1% of the time, with incidence estimates of 0.27%–1.14%. This supports its rarity, but the cited range extends above 1%, so the source does not establish a strict incidence below 1%. (LLM, conf=0.86)

    Experimental — accuracy not yet measured

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Cited by

Sorted by citations

Authors
Baik, A. H., Oluwole, O. O., Johnson, D. B., Shah, N., Salem, J.-E., Tsai, K. K., & Moslehi, J. J.
Affiliations
  • University of California, San Francisco (US)
  • Vanderbilt University Medical Center (US)
  • Sorbonne Université (FR)
Venue
Circulation Research
Published
2021-05-28
Volume
128
Issue
11
Pages
1780-1801
ISSN
  • 0009-7330 (ISSN-L)
  • 1524-4571
OpenAlex
W3157918517
Cited by
138
References
22
Citations by year
2026: 33 · 2025: 28 · 2024: 36 · 2023: 18 · 2022: 20 · 2021: 3
FWCI
3.76
Type
journal article
Language
en
Open access
Locations
  • Circulation Research (publishedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
  • HAL (submittedVersion)
  • eScholarship (California Digital Library) (submittedVersion)
Funders
  • HHS National Institutes of Health (T32 HL007731-28, R01HL41446 and)
  • HHS | National Institutes of Health (R01HL155990)
  • BMS
  • Incyte
  • Janssen
Topics
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Chemotherapy-induced cardiotoxicity and mitigation
  • Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
  • Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
Keywords
cardio-oncology, immune checkpoint inhibitors, bispecific T-cell engagers, CAR T-cell therapy, cytokine release syndrome, T cell activation, immune activation, cancer immunotherapy
MeSH terms
Receptors, Chimeric Antigen, Cytokine Release Syndrome, Immune Checkpoint Inhibitors, Animals, Cardiovascular Diseases, Disease Models, Animal, Dogs, Humans, Immunotherapy, Lymphocyte Activation, Neoplasms, T-Lymphocytes, Immunotherapy, Adoptive, Antibodies, Bispecific, Mice, Rats, Cardiotoxicity

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