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

688P - The efficacy of first-line chemotherapy combined with immunotherapy or anti-angiogenic therapy for advanced KRAS-mutant non-small cell lung cancer

Date

07 Dec 2024

Session

Poster Display session

Presenters

Huiping Qiang

Citation

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

Authors

H. Qiang, Y. Zhang, Y. Wang, J. Li, L. Zhang, X. Ling, S. Cao, Y. Zhou, H. Du, R. Zhong, H. Zhong

Author affiliations

  • Department Of Respiratory And Critical Care Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University, 200030 - Shanghai/CN

Resources

This content is available to ESMO members and event participants.

Abstract 688P

Background

Approximately 30% Caucasian NSCLC patients carry KRAS mutations. First-line chemotherapy combined with immunotherapy has been the standard therapeutic regimen for KRAS-mutant NSCLC patients. This population could also benefit from chemotherapy combined with anti-angiogenic therapy. However, few studies has reported on head-to-head efficacy comparisons between these two treatment strategies.

Methods

We selected patients with stage IV KRAS-mutated lung adenocarcinoma diagnosed in 2017 to 2022. Their clinical baseline characteristics, first-line treatment strategy, whether combined TP53 or STK11 mutation, PD-L1 expression level, etc. were evaluated. The correlation between these factors and progression-free survival (PFS) and overall survival (OS) were analyzed.

Results

From 1548 registered patients with lung cancer, 295 were selected with a KRAS mutation and 273 received first-line systematic therapy. Of the 273 patients, the most common KRAS mutation was KRAS G12C (34.3%). First-line chemotherapy combined with immunotherapy brought significant survival benefits (mPFS: 11.0 months vs. 4.0 months, P=0.0003; mOS: 17.0 months vs. 9.0 months, P=0.0002) compared with first-line chemotherapy combined with anti-angiogenic therapy. Among the 203 patients who received first-line chemotherapy combined with immunotherapy, PD-L1 positive NSCLC patients responded better than PD-L1 negative patients (mPFS: 11.0 months vs. 4.0 months, P=0.0004; mOS: 21.0 months vs. 11.0 months, P=0.0005). MPFS was significantly prolonged in NSCLC patients who carry KRAS G12C mutation (mPFS: 16.0 months vs. 9.0 months, P=0.040; mOS: 33.0 months vs. 16.0 months, P=0.062).

Conclusions

Compared with first-line chemotherapy combined with anti-angiogenic therapy, first-line chemotherapy combined with immunotherapy has brought significant survival benefit to advanced KRAS mutant NSCLC patients, especially for PD-L1 positive patients.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

National Natural Science Foundation of China.

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.