Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2018 Mar 1;4(3):374-378.
doi: 10.1001/jamaoncol.2017.2925.

Association of Immune-Related Adverse Events With Nivolumab Efficacy in Non-Small-Cell Lung Cancer

Affiliations

Association of Immune-Related Adverse Events With Nivolumab Efficacy in Non-Small-Cell Lung Cancer

Koji Haratani et al. JAMA Oncol. .

Abstract

Importance: 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.

Objective: To evaluate the relation of irAEs to nivolumab efficacy in NSCLC.

Design, setting, and participants: 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.

Exposures: The absence or presence of any irAE before the landmark date.

Main outcomes and measures: 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.

Results: 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.

Conclusions and relevance: 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.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: Dr Haratani has received honoraria from Ono Pharmaceutical Co Ltd, as well as lecture fees from Pfizer Japan Inc and Bristol-Myers Squibb Co Ltd. Dr Hayashi has received honoraria from AstraZeneca KK, Boehringer Ingelheim Japan Inc, Bristol-Myers Squibb Co Ltd, Eli Lilly Japan KK, Ono Pharmaceutical Co Ltd, and Taiho Pharmaceutical Co Ltd; lecture fees from Chugai Pharmaceutical Co Ltd, Kyowa Hakko Kirin Co Ltd, MSD KK, and Pfizer Japan Inc; and research funding from Ono Pharmaceutical Co Ltd. Dr Kaneda has received lecture fees from AstraZeneca KK, Boehringer Ingelheim Japan Inc, Bristol-Myers Squibb Co Ltd, Chugai Pharmaceutical Co Ltd, Eli Lilly Japan KK, and Pfizer Japan Inc. Dr Tanaka has received lecture fees from AstraZeneca KK and Merck Serono Co Ltd. Dr Nakagawa has received honoraria from Astellas Pharma Inc, AstraZeneca KK, AYUMI Pharmaceutical Corp, Boehringer Ingelheim Japan Inc, Bristol-Myers Squibb Co Ltd, Chugai Pharmaceutical Co Ltd, Daiichi Sankyo Co Ltd, Eli Lilly Japan KK, Kissei Pharmaceutical Co Ltd, Kyowa Hakko Kirin Co Ltd, MSD KK, Novartis Pharma KK, Ono Pharmaceutical Co Ltd, Pfizer Japan Inc, Showa Yakuhin Kako Co Ltd, Sym Bio Pharmaceuticals Ltd, and Taiho Pharmaceutical Co Ltd; research funding from AbbVie Inc, Astellas Pharma Inc, AstraZeneca KK, Boehringer Ingelheim Japan Inc, Bristol-Myers Squibb Co Ltd, Daiichi Sankyo Co Ltd, Eisai Co Ltd, Eli Lilly Japan KK, GlaxoSmithKline KK, Kyowa Hakko Kirin Co Ltd, Merck Serono Co Ltd, MSD KK, Novartis Pharma KK, Ono Pharmaceutical Co Ltd, Otsuka Pharmaceutical Co Ltd, Pfizer Japan Inc, Taiho Pharmaceutical Co Ltd, Takeda Pharmaceutical Co Ltd, and Yakult Honsha Co Ltd; and consulting or advisory fees from Astellas Pharma Inc, Eli Lilly Japan KK, and Ono Pharmaceutical Co Ltd. No other disclosures are reported.

Figures

Figure.
Figure.. Analysis of Survival for Patients With or Without irAEs
Kaplan-Meier curves with 6-week landmark analysis for (A) progression-free survival (B) and overall survival in patients with or without irAEs. irAEs indicates immune-related adverse events; NR, not reached.

Comment in

Similar articles

Cited by

References

    1. Borghaei H, Paz-Ares L, Horn L, et al. . Nivolumab versus docetaxel in advanced nonsquamous non-small-cell lung cancer. N Engl J Med. 2015;373(17):374-378. - PMC - PubMed
    1. Brahmer J, Reckamp KL, Baas P, et al. . Nivolumab versus docetaxel in advanced squamous-cell non-small-cell lung cancer. N Engl J Med. 2015;373(2):123-135. - PMC - PubMed
    1. Herbst RS, Baas P, Kim D-W, et al. . Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial. Lancet. 2016;387(10027):1540-1550. - PubMed
    1. Reck M, Rodríguez-Abreu D, Robinson AG, et al. ; KEYNOTE-024 Investigators . Pembrolizumab versus chemotherapy for PD-L1-positive non-small-cell lung cancer. N Engl J Med. 2016;375(19):1823-1833. - PubMed
    1. Boutros C, Tarhini A, Routier E, et al. . Safety profiles of anti-CTLA-4 and anti-PD-1 antibodies alone and in combination. Nat Rev Clin Oncol. 2016;13(8):473-486. - PubMed

MeSH terms