TY - JOUR
T1 - Cardiac side effects of molecular targeted therapies
T2 - Towards a better dialogue between oncologists and cardiologists
AU - Ederhy, Stephane
AU - Izzedine, Hassan
AU - Massard, Christophe
AU - Dufaitre, Ghislaine
AU - Spano, Jean Philippe
AU - Milano, Gerard
AU - Meuleman, Catherine
AU - Besse, Benjamin
AU - Boccara, Franck
AU - Kahyat, David
AU - Cohen, Ariel
AU - Soria, Jean Charles
PY - 2011/12/1
Y1 - 2011/12/1
N2 - Molecular targeted therapies (MTTs) have become a major component of modern management of various hematological and solid malignancies. However, some MTTs have been associated with cardiotoxicity. MTT-induced cardiovascular side effects include left ventricular systolic dysfunction, heart failure, conduction abnormalities, acute coronary syndrome, and hypertension. One of the most threatening complications of MTT, and notably of angiogenic inhibitors, is QT prolongation with the risk of torsades de pointe and sudden death. The precise incidence of cardiovascular events associated with MTT as well as their reversibility are unknown. Here, we summarize what is known about the cardiotoxicity of MTT, emphasizing MTTs that target tyrosine kinases. We have tried to provide both the basic mechanisms underlying specific cardiotoxicities (such as the interruption of specific signaling pathways leading to cardiomyocyte dysfunction and/or death), and offer guidance regarding the optimal way to detect and treat these cardiotoxicities.
AB - Molecular targeted therapies (MTTs) have become a major component of modern management of various hematological and solid malignancies. However, some MTTs have been associated with cardiotoxicity. MTT-induced cardiovascular side effects include left ventricular systolic dysfunction, heart failure, conduction abnormalities, acute coronary syndrome, and hypertension. One of the most threatening complications of MTT, and notably of angiogenic inhibitors, is QT prolongation with the risk of torsades de pointe and sudden death. The precise incidence of cardiovascular events associated with MTT as well as their reversibility are unknown. Here, we summarize what is known about the cardiotoxicity of MTT, emphasizing MTTs that target tyrosine kinases. We have tried to provide both the basic mechanisms underlying specific cardiotoxicities (such as the interruption of specific signaling pathways leading to cardiomyocyte dysfunction and/or death), and offer guidance regarding the optimal way to detect and treat these cardiotoxicities.
KW - Cardiotoxicity
KW - Heart failure
KW - Hypertension
KW - Molecular targeted agent
UR - http://www.scopus.com/inward/record.url?scp=80655127883&partnerID=8YFLogxK
U2 - 10.1016/j.critrevonc.2011.01.009
DO - 10.1016/j.critrevonc.2011.01.009
M3 - Review article
C2 - 21330149
AN - SCOPUS:80655127883
SN - 1040-8428
VL - 80
SP - 369
EP - 379
JO - Critical Reviews in Oncology/Hematology
JF - Critical Reviews in Oncology/Hematology
IS - 3
ER -