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

32P - Efficacy and safety of furmonertinib for leptomeningeal metastases from EGFR-mutant non-small cell lung cancer: A real-world retrospective study

Date

22 Mar 2024

Session

Poster Display session

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Huan Han

Citation

Annals of Oncology (2024) 9 (suppl_3): 1-53. 10.1016/esmoop/esmoop102569

Authors

H. Han, H. Tang

Author affiliations

  • Henan Cancer Hospital/Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou/CN

Resources

Login to get immediate access to this content.

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

Abstract 32P

Background

Leptomeningeal metastasis (LM) is a fatal complication of advanced non-small cell lung cancer (NSCLC). The aim of this retrospective study is to investigate the effectiveness and safety of furmonertinib in patients with advanced EGFR-mutated (EGFRm) NSCLC and LM.

Methods

Between February 2020 and March 2023, 31 patients with EGFR mutation-positive NSCLC with LM treated with furmonertinib for at least 8 weeks are eligible for this study. The objective was to assess confirmed objective response rate (ORR), disease control rate (DCR), duration of response (DoR), progression-free survival (PFS), overall survival (OS) and safety. Other efficacy assessments included baseline changes in cerebrospinal fluid (CFS) cytology and neurologic examination. Measurable lesions were assessed according to RECIST version 1.1 (RECIST 1.1). LM was assessed according to Neuro-Oncology LM (RANO-LM) criteria.

Results

The median PFS (mPFS) for the 31 patients was 11.70 months (95% CI 9.48-13.92months) and the median OS (mOS) was 18.40 months (95% CI 12.49-24.21months). The 1-year survival rate was 67%. The LM ORR and DCR were 75% and 95%, respectively, with a median DoR of 12.00 months (95% CI 7.40-16.60 months). The overall ORR and DCR were 22.6% and 93.5%, respectively, with a median DoR of 7.20 months (95% CI 3.60-10.80 months). Neurologic function improved in 18 (75.0%) of the 24 patients with abnormal baseline assessments. Logistic regression analysis showed that the therapeutic dose of furmonertinib was a positive predictor of OS in NSCLC patients harboring EGFR mutations with LM [HR: 2.679 (1.004-7.147), P=0.049]. The most common adverse events (AEs) are diarrhea, decreased appetite and rash. And are usually grade 1 to 2.

Conclusions

Our study provides real-world clinical evidence that furmonertinib shows a clinically meaningful therapeutic effect with a tolerable safety profile in patients with EGFRm NSCLC and LM. Our findings also suggest that the furmonertinib therapeutic dose may be an effective strategy for prolonging overall survival outcomes in these patients.

Legal entity responsible for the study

Henan Cancer Hospital.

Funding

Natural Science Foundation of Henan Province (No.212300410400).

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.