Immune checkpoint inhibitor-associated toxicity in advanced non-small cell lung cancer: An updated understanding of risk factors

Immune checkpoint inhibitors (ICIs), such as programmed death-1 (PD-1), programmed death-ligand 1 (PD-L1), cytotoxic T lymphocyte antigen 4 (CTLA-4) antibodies, etc, have revolutionized cancer treatment strategies, including non-small cell lung cancer (NSCLC). While these immunotherapy agents have a...

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Published inFrontiers in immunology Vol. 14; p. 1094414
Main Authors Hu, Xiangxiao, Wang, Lina, Shang, Bin, Wang, Junren, Sun, Jian, Liang, Bin, Su, Lili, You, Wenjie, Jiang, Shujuan
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 06.03.2023
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Summary:Immune checkpoint inhibitors (ICIs), such as programmed death-1 (PD-1), programmed death-ligand 1 (PD-L1), cytotoxic T lymphocyte antigen 4 (CTLA-4) antibodies, etc, have revolutionized cancer treatment strategies, including non-small cell lung cancer (NSCLC). While these immunotherapy agents have achieved durable clinical benefits in a subset of NSCLC patients, they bring in a variety of immune-related adverse events (irAEs), which involve cardiac, pulmonary, gastrointestinal, endocrine and dermatologic system damage, ranging from mild to life-threatening. Thus, there is an urgent need to better understand the occurrence of irAEs and predict patients who are susceptible to those toxicities. Herein, we provide a comprehensive review of what is updated about the clinical manifestations, mechanisms, predictive biomarkers and management of ICI-associated toxicity in NSCLC. In addition, this review also provides perspective directions for future research of NSCLC-related irAEs.
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ORCID: Wenjie You, https://orcid.org/0000-0002-8044-3914; Shujuan Jiang, https://orcid.org/0000-0003-3073-1931
Edited by: Gaurisankar Sa, Bose Institute, India
These authors have contributed equally to this work and share first authorship
Reviewed by: Yukihiro Toi, Sendai Kousei Hospital, Japan; Michael Shafique, Moffitt Cancer Center, United States
This article was submitted to Cancer Immunity and Immunotherapy, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2023.1094414