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GWAS Study

Association between genetic variants and the risk of nivolumab-induced immune-related adverse events.

Udagawa C, Nakano MH, Yoshida T et al.

36268685 PubMed ID
GWAS Study Type
622 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

UC
Udagawa C
NM
Nakano MH
YT
Yoshida T
OY
Ohe Y
KK
Kato K
MT
Mushiroda T
ZH
Zembutsu H
Chapter II

Abstract

Summary of the research findings

Aim: We sought to identify the variants that could predict the risk of nivolumab-induced immune-related adverse events (irAEs) in patients with cancer. Patients & methods: We enrolled 622 Japanese patients and carried out a genome-wide association study. The associations for 507 single nucleotide polymorphisms (SNPs) showing p < 0.001 were further investigated using an independent cohort. Results: In the combined analysis, possible associations were found for a total of 90 SNPs. Although no SNPs were identified to be significantly associated with nivolumab-induced irAEs, the SNP most strongly associated with nivolumab-induced irAEs was rs469490. Conclusion: This study is an important hypothesis-generating study to guide future studies in larger and/or other ethnic cohorts.

315 Japanese ancestry cases, 86 Japanese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

622
Total Participants
GWAS
Study Type
Yes
Replicated
205 Japanese ancestry cases, 16 Japanese ancestry controls
Replication Participants
East Asian
Ancestry
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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