Abstract
Immune-related adverse events (irAEs) have been associated with the efficacy of PD-1 (programmed cell death protein 1) inhibitors in patients with melanoma, but whether such an association exists for non-small-cell lung cancer (NSCLC) has remained unknown. To evaluate the relation of irAEs to nivolumab efficacy in NSCLC. In this study based on landmark and multivariable analyses, a total of 134 patients with advanced or recurrent NSCLC who were treated with nivolumab in the second-line setting or later between December 2015 and August 2016 were identified from a review of medical records from multiple institutions, including a university hospital and community hospitals. Data were updated as of December 31, 2016. The absence or presence of any irAE before the landmark date. Kaplan-Meier curves of progression-free survival (PFS) according to the development of irAEs in 6-week landmark analysis were evaluated with the log-rank test as a preplanned primary objective. Overall survival (OS) was similarly evaluated. Multivariable analysis of both PFS and OS was performed with Cox proportional hazard regression models. In a cohort of 134 patients (median [range] age, 68 [33-85] years; 90 men [67%], 44 women [33%]), irAEs were observed in 69 of the 134 study patients (51%), including 12 patients (9%) with such events of grade 3 or 4, and 24 patients (18%) requiring systemic corticosteroid therapy. In 6-week landmark analysis, median PFS was 9.2 months (95% CI, 4.4 to not reached [NR]) and 4.8 months (95% CI, 3.0 to 7.5) (P = .04) whereas median OS was NR (95% CI, 12.3 to NR) and 11.1 months (95% CI, 9.6 to NR) (P = .01) for patients with or without irAEs, respectively. Multivariable analysis also revealed that irAEs were positively associated with survival outcome, with hazard ratios of 0.525 (95% CI, 0.287 to 0.937; P = .03) for PFS and 0.282 (95% CI, 0.101 to 0.667; P = .003) for OS. Development of irAEs was associated with survival outcome of nivolumab treatment in patients with advanced or recurrent NSCLC. Further studies are needed to confirm our findings.
MeSH Terms
Adult
Aged
Aged, 80 and over
Biomarkers, Pharmacological
Biomarkers, Tumor
Carcinoma, Non-Small-Cell Lung/diagnosis,drug therapy,epidemiology,pathology
Chemotherapy, Adjuvant/adverse effects
Cohort Studies
Drug-Related Side Effects and Adverse Reactions/epidemiology
Female
Humans
Immune System Diseases/chemically induced,epidemiology
Immunotherapy/methods,statistics & numerical data
Lung Neoplasms/diagnosis,drug therapy,epidemiology,pathology
Male
Middle Aged
Nivolumab/administration & dosage,adverse effects
Prognosis
Retrospective Studies
Treatment Outcome
Chemicals
Biomarkers, Pharmacological
Biomarkers, Tumor
Nivolumab
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Haratani Koji
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Hayashi Hidetoshi
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Chiba Yasutaka
Clinical Research Center, Kindai University Hospital, Osaka-Sayama, Japan.
Kudo Keita
Department of Medical Oncology and Respiratory Medicine, National Hospital Organization Osaka Minami Medical Center, Kawachinagano, Japan.
Yonesaka Kimio
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kato Ryoji
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Kaneda Hiroyasu
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan. | Department of Medical Oncology, Kishiwada City Hospital, Kishiwada, Japan.
Hasegawa Yoshikazu
Department of Medical Oncology, Izumi Municipal Hospital, Izumi, Japan.
Tanaka Kaoru
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Takeda Masayuki
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
Nakagawa Kazuhiko
Department of Medical Oncology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.
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