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Impact of Checkpoint Inhibitor Pneumonitis on Survival in NSCLC Patients Receiving Immune Checkpoint Immunotherapy
Authors:Karthik Suresh  Kevin J. Psoter  Khinh Ranh Voong  Bairavi Shankar  Patrick M. Forde  David S. Ettinger  Kristen A. Marrone  Ronan J. Kelly  Christine L. Hann  Benjamin Levy  Josephine L. Feliciano  Julie R. Brahmer  David Feller-Kopman  Andrew D. Lerner  Hans Lee  Lonny Yarmus  Russell K. Hales  Franco D’Alessio  Jarushka Naidoo
Affiliation:1. Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland;2. Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland;3. Department of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland;4. Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland;5. Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland
Abstract: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.
Keywords:Corresponding author. Address for correspondence: Karthik Suresh   MD   Johns Hopkins Asthma and Allergy Building   5501 Hopkins Bayview Circle   Baltimore   Maryland 21224.
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