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

148P - Neoadjuvant EGFR-TKI combined with chemotherapy improves the complete response rate in operable EGFR-mutant NSCLC patients: A multicenter real-world study

Date

22 Mar 2024

Session

Poster Display session

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

WANPU YAN

Citation

Annals of Oncology (2024) 9 (suppl_3): 1-12. 10.1016/esmoop/esmoop102573

Authors

W. YAN1, Z. Zhao2, M. Fan1, L. Dai3, Y. Fang1, X. Yang1, H. Fu1, K. Chen3

Author affiliations

  • 1 Peking University Cancer Hospital & Institute, Beijing/CN
  • 2 Sun Yat-sen University Cancer Center, Guangzhou/CN
  • 3 Peking University Cancer Hospital and Institute, Beijing/CN

Resources

Login to get immediate access to this content.

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

Abstract 148P

Background

The FLAURA2 study confirmed that EGFR-TKI combined chemotherapy improved the objective response rate of patients with advanced EGFR mutant NSCLC than targeted monotherapy, and the efficacy of neoadjuvant targeted therapy for operable patients was not ideal. Therefore, we aim to evaluate the efficacy and safety of neoadjuvant EGFR-TKI combined with chemotherapy in operable EGFR mutant NSCLC patients.

Methods

Patients with EGFR mutations receiving neoadjuvant chemotherapy and targeted therapy followed by resection were included in the prospective databases in two high-volume cancer centers. We evaluated the MPR rate, pCR rate, and treatment safety, and performed survival analysis using the Kaplan-Meier curve and Cox regression model.

Results

In total, 30 patients were enrolled, most were female (n=19, 63.3%), and the median age was 60 years.10 pts were C-stage II and 20 pts were C-stage III. The majority subtype of EGFR mutation was exon-19 deletion (n=16, 53.3%), followed by the exon-21 L858R mutation (n=11, 36.7%). The most frequent EGFR-TKI was 3rd-generation (n=20, 66.7%), followed by 2nd-generation (n=9, 30.0%), and the regimens of chemotherapy were pemetrexed plus carboplatin. The preoperative TKI exposure duration ranged from 1 month to 11 months. the cycles of neoadjuvant chemotherapy ranged from 1 to 4. Grade 3–4 treatment-related AE rates were 10%. The objective response rate (ORR) was 73.3% (22 / 30), and 23 out of 30 patients achieved down-staging (76.7%). The R0 resection rate was 96.7% (29/30), and 80% was VATS. The pCR rate was 20% (6/30) and the MPR rate was 36.7% (11/30). 22 patients received adjuvant therapy. 5 patients (16.7%) developed relapse (median follow-up, 26.2 mo), and the 2-y DFS rate was 76%.

Conclusions

Combining EGFR-TKI with chemotherapy in the preoperative setting could improve pCR and MPR rates of the operable NSCLC patients with EGFR mutations, and this strategy was safe and feasible. Our results need to be validated by future prospective RCT trials.

Legal entity responsible for the study

The authors.

Funding

National Key R&D Program 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.