Impact of Checkpoint Inhibitor Pneumonitis on Survival in NSCLC Patients Receiving Immune Checkpoint Immunotherapy.
Adenocarcinoma of Lung
/ drug therapy
Aged
Antineoplastic Agents, Immunological
/ adverse effects
Carcinoma, Non-Small-Cell Lung
/ drug therapy
Carcinoma, Squamous Cell
/ drug therapy
Cell Cycle Checkpoints
/ drug effects
Female
Follow-Up Studies
Humans
Immunotherapy
/ adverse effects
Incidence
Lung Neoplasms
/ drug therapy
Male
Maryland
/ epidemiology
Pneumonia
/ chemically induced
Prognosis
Retrospective Studies
Survival Rate
Journal
Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer
ISSN: 1556-1380
Titre abrégé: J Thorac Oncol
Pays: United States
ID NLM: 101274235
Informations de publication
Date de publication:
03 2019
03 2019
Historique:
received:
02
10
2018
revised:
12
11
2018
accepted:
14
11
2018
pubmed:
7
12
2018
medline:
17
4
2020
entrez:
4
12
2018
Statut:
ppublish
Résumé
With increasing use of immune checkpoint inhibitors (ICIs) for advanced NSCLC, there is increasing recognition of immune-related adverse events associated with ICI use. We recently reported increased incidence of checkpoint inhibitor pneumonitis (CIP) in ICI-treated NSCLC patients. Since development of immune-related adverse events in other organ systems has been associated with either no change or even improvement in tumor response/cancer outcomes, we sought to better understand the impact of CIP development on overall survival in ICI-treated NSCLC patients. Using baseline and follow-up data collected on a cohort of 205 ICI-treated NSCLC patients, we used a multi-state modeling approach to understand the effect of developing CIP on the risk of death. We observed time-dependent changes in risk of developing and recovery from CIP, with an increased risk of both developing and recovering from CIP in the first year after initiating ICI. We found that developing CIP independently increased the risk of transitioning to death in both adjusted and unadjusted models. In the multivariate model, we found that the increase in mortality associated with CIP was only seen in patients with adenocarcinoma tumor histology. Collectively, these findings suggest that in NSCLC, development of CIP worsens survival in patients receiving immunotherapy.
Identifiants
pubmed: 30503891
pii: S1556-0864(18)33493-2
doi: 10.1016/j.jtho.2018.11.016
pii:
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
494-502Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2018 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.