Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 03

1045P - The association of human leukocyte antigen variants in immune-related toxicity and efficacy in Chinese lung cancer patients treated with immune checkpoint inhibitors

Date

14 Sep 2024

Session

Poster session 03

Topics

Immunotherapy

Tumour Site

Presenters

Yongchang Zhang

Citation

Annals of Oncology (2024) 35 (suppl_2): S674-S711. 10.1016/annonc/annonc1596

Authors

Y. Zhang1, H. Yan1, Z. Liang1, G. Zhou2, Y. Wu1, H. Qin1, N. Yang1, Z. Huang1, D. Yang1, Y. Zhang1, K. Graham-Siegenthaler3, R. Walls3, S. Hamzic3, Y. He3, R. Mohindra3, Z. Li4, R. Luo5, A. Saha6, C. Hammer6, G.S. Chandler7

Author affiliations

  • 1 Lung Cancer And Gastrointestinal Unit, Hunan Cancer Hospital, 410013 - Changsha/CN
  • 2 Dermatology Department, XIANGYA HOSPITAL CENTRAL SOUTH UNIVERSITY, 410008 - changsha/CN
  • 3 Pharma Development Department, F. Hoffmann-La Roche AG, 4070 - Basel/CH
  • 4 Medical Advisor, Shanghai Roche Pharmaceuticals Ltd., 201203 - Shanghai/CN
  • 5 Roche International Patient Safety Team, Shanghai Roche Pharmaceuticals Ltd., 201203 - Shanghai/CN
  • 6 Parma Development Department, Genentech, Inc., 94080 - South San Francisco/US
  • 7 Drug Safety, F. Hoffmann-La Roche AG, 4070 - Basel/CH

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1045P

Background

Previous studies in European populations have indicated an association between Human Leukocyte Antigen (HLA) allelic variations and efficacy as well as the risk of immune-related adverse events (irAEs) during immune checkpoint inhibitor (ICI) use in lung cancer patients (pts). Limited exploration of these relationships has been done in pts of Asian ancestry.

Methods

A case-control study was conducted with 1807 subjects from 3261 lung cancer pts who received at least one cycle of ICI, any regimen, between January 2018 and December 2023 at Hunan Cancer Hospital. 248 pts with immune-related pneumonitis (IRP) and 380 pts with immune-related hepatitis (IRH) were identified and control cohorts without those irAEs were randomly selected at a 1:3 ratio (744 pts for IRP, 1140 pts for IRH). Illumina Asian Screening Arrays and CookHLA was used for HLA genotyping. Multivariable logistic regression models adjusting for baseline factors were used for HLA-irAE analysis, while multivariable Cox proportional hazards models were used for the association between HLA and overall survival (OS) (allele frequency >2%).

Results

The median onset time for IRP and IRH was 5.9 and 2.1 months, respectively. Analysis of baseline characteristics revealed significant differences in the line of ICI and treatment strategy for the IRH cohorts. No HLA alleles were found to be associated with either of the irAEs or OS at an FDR of <0.05. However, at FDR < 0.1, HLA-A*02:07 (OR:3.19, 95%CI: 1.61-6.36, p<0.001, FDR:0.06) and HLA-DQB1*05:01 (OR:3.45, 95%CI: 1.47-7.39, p=0.002, FDR:0.09) were suggestive of higher risk of developing severe (grade ≥3) IRH (n=62). Furthermore, HLA-DQB1*06:01 (HR:1.35, 95%CI: 1.13-1.62, p<0.001, FDR:0.07) was suggestive of poor OS, while HLA-DQB1*03:01 (HR:0.79, 95%CI: 0.68-0.92, p=0.003, FDR:0.09) was suggestive of improved OS.

Conclusions

This case-controlled real-world study, the largest of its kind in the Chinese population, suggested that certain HLA alleles might be linked to the incidence of severe IRH and overall survival in Chinese lung cancer pts treated with ICI. Further research is needed to confirm the findings.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

This research was supported by F. Hoffmann-La Roche Ltd., which provided grant support mainly on the sample sequencing and study operation according to local laws and regulations.

Disclosure

All authors have declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.