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

654P - Efficacy and safety of first-line ipilimumab and nivolumab treatment in elderly patients with non-small cell lung cancer

Date

07 Dec 2024

Session

Poster Display session

Presenters

Hisao Imai

Citation

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

Authors

H. Imai1, A. Mouri1, S. Endo2, K. Tsukamoto3, K. Masaki1, K. Hashimoto1, Y. Miura1, A. Shiono1, O. Yamaguchi1, J. Nakagawa4, K. Kaira1, K. Kobayashi1, H. Kagamu1

Author affiliations

  • 1 Respiratory Medicine, Saitama Medical University, 350-1298 - Saitama/JP
  • 2 Respiratory Medicine, Gunma Prefectural Cancer Center, 373-0828 - Ota/JP
  • 3 Respiratory Medicine, National Hospital Organization Disaster Medical Center, 190-0014 - Tachikawa/JP
  • 4 Respiratory Medicine, National Hospital Organization Takasaki General Medical Center, 370-0829 - Takasaki/JP

Resources

This content is available to ESMO members and event participants.

Abstract 654P

Background

Ipilimumab and nivolumab (ipi-nivo) combination therapy is an effective first-line treatment for advanced non-small cell lung cancer (NSCLC), regardless of programmed death ligand 1 expression. However, the effectiveness and feasibility of first-line ipi-nivo therapy in elderly patients (aged ≥75 years) is unclear. Therefore, this study aimed to investigate the efficacy and safety of first-line ipi-nivo therapy in elderly patients with NSCLC.

Methods

We retrospectively evaluated the data of patients with NSCLC, aged ≥75 years, who were treated with first-line ipi-nivo from December 2020 to November 2022 at four institutes in Japan. Data on patient characteristics, efficacy of ipi-nivo therapy, and type and severity of adverse events were assessed.

Results

Fifty-seven patients (52 men and 5 women; median age, 78 years [range: 75–86]) were included in the analysis. The overall response rate was 42.1%, disease control rate was 73.6%, median progression-free survival (PFS) was 7.1 months, and median overall survival (OS) was 14.1 months. Frequent adverse events of Grade 3 or higher were pneumonitis in 7 patients (12.2%), increased aspartate transaminase in 4 patients (7.0%), increased alanine transaminase in 4 patients (7.0%), adrenal insufficiency in 3 patients (5.3%), and colitis in 3 patients (5.3%). No treatment-related deaths occurred. First-line ipi-nivo treatment was associated with PFS based on the presence or absence of immune-related adverse events (irAEs). The PFS of patients with irAEs was 11.7 months, whereas the PFS of patients without irAEs was 2.8 months.

Conclusions

First-line ipi-nivo therapy was effective in elderly patients with NSCLC. While there was a trend towards increased pneumonitis, the therapy manageable and suggested as a viable treatment option.

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.