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 Display session

715P - Impact of serum anti-p53 antibody on efficacy of immune checkpoint inhibitors in advanced non-small cell lung cancer

Date

07 Dec 2024

Session

Poster Display session

Presenters

Tetsuo Shimizu

Citation

Annals of Oncology (2024) 35 (suppl_4): S1632-S1678. 10.1016/annonc/annonc1698

Authors

T. Shimizu, Y. Nakagawa, Y. Asai

Author affiliations

  • Division Of Respiratory Medicine, Department Of Internal Medicine, Nihon University School of Medicine, 173-8610 - Tokyo/JP

Resources

This content is available to ESMO members and event participants.

Abstract 715P

Background

In the treatment of lung cancer with immune checkpoint inhibitors (ICI), there is a need for predictive therapeutic biomarkers that can be measured noninvasively. Various autoantibodies have been detected in cancer patient sera, among which anti-p53 antibodies are associated with p53 gene mutations. p53 gene mutations have been reported to be associated with efficacy of ICI, however, it is unclear whether anti-p53 antibodies affect the antitumor effect of ICI.

Methods

Participants were patients with advanced non-small cell lung cancer who received ICI at our hospital from November 2018 to May 2022. Blood samples were obtained before and after treatment with ICI and serum anti-p53 antibody levels were measured. The relationship between serum anti-p53 antibody and treatment response (response, progression-free survival, and overall survival) to ICI was investigated.

Results

A total of 166 patients were enrolled. Median age was 69.4 (range, 43-90), 30.1% (50/166) were females. PD-L1 TPS ≥50%/1-49%/<1%/unknown included 54 (32.5%)/45 (27.1%)/34 (20.5%)/33 (19.9%), respectively. Serum anti-p53 antibody positive rate (p53+) before treatment was 17.5% (29/166). No significant differences in patient characteristics between p53+ and p53- groups. Patients in the p53+ group tended to have shorter PFS (HR 1.37, 95%CI 0.83-2.3, p=0.215) than those in the p53- group. 16 patients in the p53+ group had a decrease in p53 antibody levels after treatment with ICI ± chemotherapy. Serum anti-p53 antibody levels varied with treatment with ICI ± chemotherapy. Patients with decrease in p53 antibody levels after treatment had significantly longer PFS (HR 5.03, 95%CI 1.92-13.24, p=0.001) than those with not decrease.

Conclusions

We believe serum p53 antibody could be useful as a predictor of therapeutic efficacy of ICI for advanced non-small cell lung cancer.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

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.