Cardiovascular disease and chimeric antigen receptor cellular therapy
- PMID: 36211558
- PMCID: PMC9538377
- DOI: 10.3389/fcvm.2022.932347
Cardiovascular disease and chimeric antigen receptor cellular therapy
Abstract
Chimeric antigen receptor T-cell (CAR T) therapy is a revolutionary personalized therapy that has significantly impacted the treatment of patients with hematologic malignancies refractory to other therapies. Cytokine release syndrome (CRS) is a major side effect of CAR T therapy that can occur in 70-90% of patients, with roughly 40% of patients at grade 2 or higher. CRS can cause an intense inflammatory state leading to cardiovascular complications, including troponin elevation, arrhythmias, hemodynamic instability, and depressed left ventricular systolic function. There are currently no standardized guidelines for the management of cardiovascular complications due to CAR T therapy, but systematic practice patterns are emerging. In this review, we contextualize the history and indications of CAR T cell therapy, side effects related to this treatment, strategies to optimize the cardiovascular health prior to CAR T and the management of cardiovascular complications related to CRS. We analyze the existing data and discuss potential future approaches.
Keywords: cardio-oncology; cardiovascular disease; cellular therapy; chimeric antigen receptor (CAR T); cytokine release syndrome (CRS); immunotherapy.
Copyright © 2022 Rao, Stewart, Eljalby, Ramakrishnan, Anderson, Awan, Chandra, Vallabhaneni, Zhang and Zaha.
Conflict of interest statement
Author FA has provided consultancy to: Genentech, Astrazeneca, Abbvie, Janssen, Pharmacyclics, Gilead sciences, Kite pharma, Celgene, Karyopharm, MEI Pharma, Verastem, Incyte, Beigene, Johnson and Johnson, Dava Oncology, BMS, Merck, Cardinal Health, ADCT therapeutics, and Epizyme. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Figures
Similar articles
-
Cardiac adverse events after Chimeric Antigen Receptor (CAR) T cell therapies: an updated systematic review and meta-analysis.Cardiooncology. 2024 Aug 20;10(1):52. doi: 10.1186/s40959-024-00252-y. Cardiooncology. 2024. PMID: 39164789 Free PMC article. Review.
-
Cardiovascular Complications of Chimeric Antigen Receptor T-Cell Therapy: The Cytokine Release Syndrome and Associated Arrhythmias.J Immunother Precis Oncol. 2020 Jul 20;3(3):113-120. doi: 10.36401/JIPO-20-10. eCollection 2020 Aug. J Immunother Precis Oncol. 2020. PMID: 35663258 Free PMC article. Review.
-
Cardiovascular Events Among Adults Treated With Chimeric Antigen Receptor T-Cells (CAR-T).J Am Coll Cardiol. 2019 Dec 24;74(25):3099-3108. doi: 10.1016/j.jacc.2019.10.038. J Am Coll Cardiol. 2019. PMID: 31856966 Free PMC article.
-
Cardiotoxicity from chimeric antigen receptor-T cell therapy for advanced malignancies.Eur Heart J. 2022 May 21;43(20):1928-1940. doi: 10.1093/eurheartj/ehac106. Eur Heart J. 2022. PMID: 35257157 Free PMC article. Review.
-
Impact of cytokine release syndrome on cardiac function following CD19 CAR-T cell therapy in children and young adults with hematological malignancies.J Immunother Cancer. 2020 Sep;8(2):e001159. doi: 10.1136/jitc-2020-001159. J Immunother Cancer. 2020. PMID: 32883871 Free PMC article.
Cited by
-
Cardiac adverse events after Chimeric Antigen Receptor (CAR) T cell therapies: an updated systematic review and meta-analysis.Cardiooncology. 2024 Aug 20;10(1):52. doi: 10.1186/s40959-024-00252-y. Cardiooncology. 2024. PMID: 39164789 Free PMC article. Review.
-
Toxicity of CAR T-Cell Therapy for Multiple Myeloma.Acta Haematol. 2025;148(3):300-314. doi: 10.1159/000539134. Epub 2024 May 8. Acta Haematol. 2025. PMID: 38718775 Free PMC article. Review.
-
Cardiotoxic Effects Following CAR-T Cell Therapy: A Literature Review.Curr Oncol Rep. 2025 Feb;27(2):135-147. doi: 10.1007/s11912-024-01634-2. Epub 2025 Jan 21. Curr Oncol Rep. 2025. PMID: 39836349 Free PMC article. Review.
-
T cells in cardiac health and disease.J Clin Invest. 2025 Jan 16;135(2):e185218. doi: 10.1172/JCI185218. J Clin Invest. 2025. PMID: 39817455 Free PMC article. Review.
-
Soluble Urokinase-Type Plasminogen Activator Receptor (suPAR), Growth Differentiation Factor-15 (GDF-15), and Soluble C5b-9 (sC5b-9) Levels Are Significantly Associated with Endothelial Injury Indices in CAR-T Cell Recipients.Int J Mol Sci. 2024 Oct 14;25(20):11028. doi: 10.3390/ijms252011028. Int J Mol Sci. 2024. PMID: 39456810 Free PMC article.
References
-
- Lorenz E, Uphoff D, Reid TR, Shelton E. Modification of irradiation injury in mice and guinea pigs by bone marrow injections. J Natl Cancer Inst. (1951) 12:197–201. - PubMed
-
- Rosenberg SA, Lotze MT, Muul LM, Leitman S, Chang AE, Ettinghausen SE, et al. . Observations on the systemic administration of autologous lymphokine-activated killer cells and recombinant interleukin-2 to patients with metastatic cancer. N Engl J Med. (1985) 313:1485–92. 10.1056/NEJM198512053132327 - DOI - PubMed
Publication types
LinkOut - more resources
Full Text Sources