Therapeutic and Prognostic Implications of Immune-Related Adverse Events in Advanced Non-Small-Cell Lung Cancer.
immune-checkpoint inhibitors
immune-related adverse events
immunotherapy
lethality
prognosis
treatment interruption
Journal
Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867
Informations de publication
Date de publication:
2021
2021
Historique:
received:
30
04
2021
accepted:
09
06
2021
entrez:
16
7
2021
pubmed:
17
7
2021
medline:
17
7
2021
Statut:
epublish
Résumé
PD-(L)1 inhibitors have improved prognosis of non-small-cell lung cancer (NSCLC), but can also cause immune-related adverse events (irAEs) that complicate management. We analyzed NSCLC patients receiving PD-(L)1 inhibitors from 2012 to 2020 in a German academic center. IrAE showed comparable frequencies in stage IV (198/894 or 22%) Approximately one-fourth of immunotherapy-treated NSCLC patients develop irAEs, most of which necessitate treatment suspension and steroids. Despite more frequent occurrence with PD-L1 positive tumors, lower NLR, and better ECOG PS, irAEs are independently associated with longer survival, especially when affecting the skin. Lethality is below 1%.
Identifiants
pubmed: 34268127
doi: 10.3389/fonc.2021.703893
pmc: PMC8277237
doi:
Types de publication
Journal Article
Langues
eng
Pagination
703893Informations de copyright
Copyright © 2021 Daniello, Elshiaty, Bozorgmehr, Kuon, Kazdal, Schindler, Shah, Volckmar, Lusky, Diekmann, Liersch, Faehling, Muley, Kriegsmann, Benesova, Stenzinger, Thomas and Christopoulos.
Déclaration de conflit d'intérêts
FB: research funding from BMS and travel grants from BMS and MSD. JK: research funding from AstraZeneca and Celgene. DK: advisory board and speaker’s honoraria from AstraZeneca, BMS, Pfizer. RS: research funding from BMS. KB: research funding from Novartis and Abbvie, speaker’s honoraria/advisory board/travel grants from Abbvie, BMS, Gilead/Galapagos, Janssen, Lilly, Medac, MSD, Mundipharma, Novartis, Pfizer, Roche, UCB. AS: advisory board honoraria from BMS, AstraZeneca, ThermoFisher, Novartis, speaker’s honoraria from BMS, Illumina, AstraZeneca, Novartis, ThermoFisher, MSD, Roche, and research funding from Chugai. MT: advisory board honoraria from Novartis, Lilly, BMS, MSD, Roche, Celgene, Takeda, AbbVie, Boehringer, speaker’s honoraria from Lilly, MSD, Takeda, research funding from AstraZeneca, BMS, Celgene, Novartis, Roche and travel grants from BMS, MSD, Novartis, Boehringer. PC: research funding from AstraZeneca, Novartis, Roche, Takeda, and advisory board/lecture fees from AstraZeneca, Boehringer Ingelheim, Chugai, Novartis, Pfizer, Roche, Takeda. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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