TY - JOUR
T1 - Cardiotoxicities of Chimeric Antigen Receptor T-Cell Therapy and Bispecific T-Cell Antibodies
AU - Qamer, Syed Zyad
AU - Miraglia, Genie M.
AU - Granville, Matthew J.
AU - Finkelstein, Alexa
AU - Okin, Emily
AU - Mahmood, Syed Saad
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024.
PY - 2024/7
Y1 - 2024/7
N2 - Purpose of Review: Chimeric antigen receptor T-cells (CAR-T) and bispecific antibodies (BiTE) are novel therapies used to treat hematologic malignancies, lung cancer and melanoma. With the increasing use of these novel therapies, the incidence and prognosis of their cardiovascular side effects needs to be further elucidated. Recent Findings: Randomized trials have highlighted the systemic effects of CAR-T and BiTE therapy including cytokine release syndrome (CRS) and resultant hypotension and respiratory failure. Cohort studies have elucidated the cardiovascular effects associated with CAR-T and BiTE therapy including heart failure, cardiomyopathy, arrythmia, myocardial infarction, stroke and cardiovascular death. Summary: Cardiovascular events after CAR-T and BiTE therapy can occur and are often associated with CRS. CAR-T recipients experiencing severe cardiovascular events may have worse survival. Further prospective studies are needed to understand the full scope of cardiovascular effects and mitigation strategies for these therapies.
AB - Purpose of Review: Chimeric antigen receptor T-cells (CAR-T) and bispecific antibodies (BiTE) are novel therapies used to treat hematologic malignancies, lung cancer and melanoma. With the increasing use of these novel therapies, the incidence and prognosis of their cardiovascular side effects needs to be further elucidated. Recent Findings: Randomized trials have highlighted the systemic effects of CAR-T and BiTE therapy including cytokine release syndrome (CRS) and resultant hypotension and respiratory failure. Cohort studies have elucidated the cardiovascular effects associated with CAR-T and BiTE therapy including heart failure, cardiomyopathy, arrythmia, myocardial infarction, stroke and cardiovascular death. Summary: Cardiovascular events after CAR-T and BiTE therapy can occur and are often associated with CRS. CAR-T recipients experiencing severe cardiovascular events may have worse survival. Further prospective studies are needed to understand the full scope of cardiovascular effects and mitigation strategies for these therapies.
KW - Bi-specific antibodies
KW - CAR T-cell therapy
KW - Cardiotoxicity
UR - http://www.scopus.com/inward/record.url?scp=85193929183&partnerID=8YFLogxK
U2 - 10.1007/s11936-024-01041-7
DO - 10.1007/s11936-024-01041-7
M3 - Review article
AN - SCOPUS:85193929183
SN - 1092-8464
VL - 26
SP - 175
EP - 187
JO - Current Treatment Options in Cardiovascular Medicine
JF - Current Treatment Options in Cardiovascular Medicine
IS - 7
ER -