TY - JOUR
T1 - Immune Checkpoint Inhibitor Therapy in Oncology
T2 - Current Uses and Future Directions: JACC: CardioOncology State-of-the-Art Review
AU - Tan, Sean
AU - Day, Daphne
AU - Nicholls, Stephen J.
AU - Segelov, Eva
N1 - Funding Information:
The authors wish to thank Professor Nitesh Nerlekar (Victorian Heart Institute) for his assistance with technical editing and proofreading of the manuscript.
Publisher Copyright:
© 2022 The Authors
PY - 2022/12
Y1 - 2022/12
N2 - Immune checkpoint inhibitors (ICIs) are a major class of immuno-oncology therapeutics that have significantly improved the prognosis of various cancers, both in (neo)adjuvant and metastatic settings. Unlike other conventional therapies, ICIs elicit antitumor effects by enhancing host immune systems to eliminate cancer cells. There are 3 approved ICI classes by the U.S. Food and Drug Administration: inhibitors targeting cytotoxic T lymphocyte associated antigen 4, programmed death 1/programmed death-ligand 1, and lymphocyte-activation gene 3, with many more in development. ICIs are commonly associated with distinct toxicities, known as immune-related adverse events, which can arise during treatment or less frequently be of late onset, usually relating to excessive activation of the immune system. Acute cardiovascular immune-related adverse events such as myocarditis are rare; however, data suggesting chronic cardiovascular sequelae are emerging. This review presents the current landscape of ICIs in oncology, with a focus on important aspects relevant to cardiology.
AB - Immune checkpoint inhibitors (ICIs) are a major class of immuno-oncology therapeutics that have significantly improved the prognosis of various cancers, both in (neo)adjuvant and metastatic settings. Unlike other conventional therapies, ICIs elicit antitumor effects by enhancing host immune systems to eliminate cancer cells. There are 3 approved ICI classes by the U.S. Food and Drug Administration: inhibitors targeting cytotoxic T lymphocyte associated antigen 4, programmed death 1/programmed death-ligand 1, and lymphocyte-activation gene 3, with many more in development. ICIs are commonly associated with distinct toxicities, known as immune-related adverse events, which can arise during treatment or less frequently be of late onset, usually relating to excessive activation of the immune system. Acute cardiovascular immune-related adverse events such as myocarditis are rare; however, data suggesting chronic cardiovascular sequelae are emerging. This review presents the current landscape of ICIs in oncology, with a focus on important aspects relevant to cardiology.
KW - biomarkers
KW - cardio-oncology
KW - cardiotoxicity
KW - immune checkpoint inhibitors
KW - immune related adverse events
KW - immunotherapy
KW - medical oncology
UR - http://www.scopus.com/inward/record.url?scp=85143989203&partnerID=8YFLogxK
U2 - 10.1016/j.jaccao.2022.09.004
DO - 10.1016/j.jaccao.2022.09.004
M3 - Review Article
C2 - 36636451
AN - SCOPUS:85143989203
SN - 2666-0873
VL - 4
SP - 579
EP - 597
JO - JACC: CardioOncology
JF - JACC: CardioOncology
IS - 5
ER -