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Impact of Checkpoint Inhibitor Pneumonitis on Survival in NSCLC Patients Receiving Immune Checkpoint Immunotherapy.
Suresh, Karthik; Psoter, Kevin J; Voong, Khinh Ranh; Shankar, Bairavi; Forde, Patrick M; Ettinger, David S; Marrone, Kristen A; Kelly, Ronan J; Hann, Christine L; Levy, Benjamin; Feliciano, Josephine L; Brahmer, Julie R; Feller-Kopman, David; Lerner, Andrew D; Lee, Hans; Yarmus, Lonny; Hales, Russell K; D'Alessio, Franco; Danoff, Sonye K; Naidoo, Jarushka.
Afiliação
  • Suresh K; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland. Electronic address: ksuresh2@jhmi.edu.
  • Psoter KJ; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Voong KR; Department of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Shankar B; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Forde PM; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Ettinger DS; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Marrone KA; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Kelly RJ; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Hann CL; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Levy B; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Feliciano JL; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Brahmer JR; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Feller-Kopman D; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Lerner AD; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Lee H; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Yarmus L; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Hales RK; Department of Radiation Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • D'Alessio F; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Danoff SK; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Naidoo J; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
J Thorac Oncol ; 14(3): 494-502, 2019 03.
Article em En | MEDLINE | ID: mdl-30503891
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male País/Região como assunto: America do norte Idioma: En Ano de publicação: 2019 Tipo de documento: Article