» Articles » PMID: 36211558

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.

Citing Articles

Cardiotoxic Effects Following CAR-T Cell Therapy: A Literature Review.

Joseph T, Sanchez J, Abbasi A, Zhang L, Sica R, Duong T Curr Oncol Rep. 2025; 27(2):135-147.

PMID: 39836349 PMC: 11861112. DOI: 10.1007/s11912-024-01634-2.


T cells in cardiac health and disease.

Martin P, Sanchez-Madrid F J Clin Invest. 2025; 135(2.

PMID: 39817455 PMC: 11735099. DOI: 10.1172/JCI185218.


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.

Gavriilaki E, Demosthenous C, Evangelidis P, Bousiou Z, Batsis I, Vardi A Int J Mol Sci. 2024; 25(20).

PMID: 39456810 PMC: 11507105. DOI: 10.3390/ijms252011028.


Cardiac adverse events after Chimeric Antigen Receptor (CAR) T cell therapies: an updated systematic review and meta-analysis.

Maleki S, Esmaeili Z, Seighali N, Shafiee A, Montazeri Namin S, Tofighi Zavareh M Cardiooncology. 2024; 10(1):52.

PMID: 39164789 PMC: 11334556. DOI: 10.1186/s40959-024-00252-y.


Revisiting treatment-related cardiotoxicity in patients with malignant lymphoma-a review and prospects for the future.

Rihackova E, rihacek M, Vyskocilova M, Valik D, Elbl L Front Cardiovasc Med. 2023; 10:1243531.

PMID: 37711551 PMC: 10499183. DOI: 10.3389/fcvm.2023.1243531.

References
1.
Munshi N, Anderson Jr L, Shah N, Madduri D, Berdeja J, Lonial S . Idecabtagene Vicleucel in Relapsed and Refractory Multiple Myeloma. N Engl J Med. 2021; 384(8):705-716. DOI: 10.1056/NEJMoa2024850. View

2.
Herrmann J, Lenihan D, Armenian S, Barac A, Blaes A, Cardinale D . Defining cardiovascular toxicities of cancer therapies: an International Cardio-Oncology Society (IC-OS) consensus statement. Eur Heart J. 2021; 43(4):280-299. PMC: 8803367. DOI: 10.1093/eurheartj/ehab674. View

3.
Bonifant C, Jackson H, Brentjens R, Curran K . Toxicity and management in CAR T-cell therapy. Mol Ther Oncolytics. 2016; 3:16011. PMC: 5008265. DOI: 10.1038/mto.2016.11. View

4.
Steiner R, Banchs J, Koutroumpakis E, Becnel M, Gutierrez C, Strati P . Cardiovascular events in patients treated with chimeric antigen receptor T-cell therapy for aggressive B-cell lymphoma. Haematologica. 2021; 107(7):1555-1566. PMC: 9244830. DOI: 10.3324/haematol.2021.280009. View

5.
Oluwole O, Bouabdallah K, Munoz J, de Guibert S, Vose J, Bartlett N . Prophylactic corticosteroid use in patients receiving axicabtagene ciloleucel for large B-cell lymphoma. Br J Haematol. 2021; 194(4):690-700. PMC: 8457222. DOI: 10.1111/bjh.17527. View