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Pretreatment Lung Function and Checkpoint Inhibitor Pneumonitis in NSCLC.
Reuss, Joshua E; Brigham, Emily; Psoter, Kevin J; Voong, Khinh Ranh; Shankar, Bairavi; Ettinger, David S; Marrone, Kristen A; 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; Forde, Patrick M; Suresh, Karthik; Naidoo, Jarushka.
Afiliación
  • Reuss JE; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Brigham E; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Psoter KJ; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Voong KR; Department of Pediatrics, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Shankar B; Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University School of Medicine, 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.
  • Hann CL; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Levy B; 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.
  • Brahmer JR; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Feller-Kopman D; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Lerner AD; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Lee H; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Yarmus L; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Hales RK; Department of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • D'Alessio F; Bloomberg-Kimmel Institute for Cancer Immunotherapy at Johns Hopkins University, Baltimore, Maryland.
  • Danoff SK; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Forde PM; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Suresh K; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
  • Naidoo J; Division of Pulmonary Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
JTO Clin Res Rep ; 2(10): 100220, 2021 Oct.
Article en En | MEDLINE | ID: mdl-34746881
ABSTRACT

INTRODUCTION:

Checkpoint inhibitor pneumonitis (CIP) is a serious toxicity of anti-programmed death-(ligand) 1 immunotherapy. Whether pretreatment differences in pulmonary function exist in patients who develop CIP is unknown. We analyzed the pulmonary function tests (PFTs) of patients with NSCLC treated with immune checkpoint inhibitors (ICIs) to evaluate whether pretreatment lung function was associated with CIP development.

METHODS:

Patients were included if they completed greater than or equal to 1 PFT within 2 years preceding ICI initiation. CIP status (CIP+ developed CIP, CIP- did not develop CIP) was determined clinically. Generalized estimating equation-based linear regression was used to evaluate the effects of time and CIP on lung function. Primary outcomes included the following percent-predicted forced expiratory volume in 1 second (FEV1pp), percent-predicted forced vital capacity (FVCpp), and FEV1/FVC.

RESULTS:

A total of 43 patients (34 CIP-, 9 CIP+) with 79 PFTs (59 CIP-, 20 CIP+) were included. CIP+ patients had a 21.7% lower pretreatment FEV1pp compared with the CIP- group (95% confidence interval -38.6 to -4.7). No statistically significant differences in FVCpp or FEV1/FVC were observed. The prevalence of obstructive lung disease was similar in both groups at 67% and 62% for the CIP+ and CIP- cohorts, as was the prevalence of current/former smoking at 100% and 93%, respectively.

CONCLUSIONS:

Pretherapy differences in lung function were evident between patients who did and did not develop CIP, though the prevalence of obstructive lung disease was similar. Prospective studies are needed to validate these findings, inform potential risk factors for CIP, and investigate the effects of ICI treatment and CIP on pulmonary function in patients with NSCLC.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JTO Clin Res Rep Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JTO Clin Res Rep Año: 2021 Tipo del documento: Article