TY - JOUR
T1 - Chimeric Antigen Receptor T-Cell Therapy for Cancer and Heart
T2 - JACC Council Perspectives
AU - Ganatra, Sarju
AU - Carver, Joseph R.
AU - Hayek, Salim S.
AU - Ky, Bonnie
AU - Leja, Monika J.
AU - Lenihan, Daniel J.
AU - Lenneman, Carrie
AU - Mousavi, Negaresh
AU - Park, Jae H.
AU - Perales, Miguel Angel
AU - Ryan, Thomas D.
AU - Scherrer-Crosbie, Marielle
AU - Steingart, Richard M.
AU - Yang, Eric H.
AU - Zaha, Vlad
AU - Barac, Ana
AU - Liu, Jennifer E.
N1 - Publisher Copyright:
© 2019 American College of Cardiology Foundation
PY - 2019/12/24
Y1 - 2019/12/24
N2 - Chimeric antigen receptor (CAR) T-cell therapy has significantly advanced the treatment of patients with relapsed and refractory hematologic malignancies and is increasingly investigated as a therapeutic option of other malignancies. The main adverse effect of CAR T-cell therapy is potentially life-threatening cytokine release syndrome (CRS). Clinical cardiovascular (CV) manifestations of CRS include tachycardia, hypotension, troponin elevation, reduced left ventricular ejection fraction, pulmonary edema, and cardiogenic shock. Although insults related to CRS toxicity might be transient and reversible in most instances in patients with adequate CV reserve, they can be particularly challenging in higher-risk, often elderly patients with pre-existing CV disease. As the use of CAR T-cell therapy expands to include a wider patient population, careful patient selection, pre-treatment cardiac evaluation, and CV risk stratification should be considered within the CAR T-cell treatment protocol. Early diagnosis and management of CV complications in patients with CRS require awareness and multidisciplinary collaboration.
AB - Chimeric antigen receptor (CAR) T-cell therapy has significantly advanced the treatment of patients with relapsed and refractory hematologic malignancies and is increasingly investigated as a therapeutic option of other malignancies. The main adverse effect of CAR T-cell therapy is potentially life-threatening cytokine release syndrome (CRS). Clinical cardiovascular (CV) manifestations of CRS include tachycardia, hypotension, troponin elevation, reduced left ventricular ejection fraction, pulmonary edema, and cardiogenic shock. Although insults related to CRS toxicity might be transient and reversible in most instances in patients with adequate CV reserve, they can be particularly challenging in higher-risk, often elderly patients with pre-existing CV disease. As the use of CAR T-cell therapy expands to include a wider patient population, careful patient selection, pre-treatment cardiac evaluation, and CV risk stratification should be considered within the CAR T-cell treatment protocol. Early diagnosis and management of CV complications in patients with CRS require awareness and multidisciplinary collaboration.
KW - cardiotoxicity
KW - chimeric antigen receptor T-cell therapy
KW - cytokine release syndrome
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U2 - 10.1016/j.jacc.2019.10.049
DO - 10.1016/j.jacc.2019.10.049
M3 - Review article
C2 - 31856973
AN - SCOPUS:85076042932
SN - 0735-1097
VL - 74
SP - 3153
EP - 3163
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 25
ER -