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CASE REPORT article

Front. Oncol.

Sec. Thoracic Oncology

Volume 15 - 2025 | doi: 10.3389/fonc.2025.1673836

This article is part of the Research TopicReal-World Data and Real-World Evidence in Lung Cancer Volume IIView all 6 articles

Durable Clinical Benefit from Gefitinib plus Bevacizumab in a Non-Small Cell Lung Cancer Patient with an Acquired C797S Mutation Following Osimertinib Treatment: A Case Report and Literature Review

Provisionally accepted
Yuping  TanYuping TanMeng  DongMeng DongXi  LiXi LiWenbo  LiWenbo LiFei  XiongFei XiongWeidong  BaoWeidong BaoYongzhou  DaiYongzhou DaiLinjun  YueLinjun YueYuan  LiuYuan Liu*
  • Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, China

The final, formatted version of the article will be published soon.

Abstract Background: The emergence of the EGFR C797S mutation in the absence of T790M represents a common mechanism of acquired resistance to first-line Osimertinib in non-small cell lung cancer (NSCLC), posing a significant clinical challenge. Case Presentation: We present the case of a 72-year-old male diagnosed with metastatic NSCLC harboring an EGFR exon 19 deletion, who developed an acquired C797S mutation (without T790M) following 25 months of first-line Osimertinib therapy. Based on this molecular profile, the patient received a regimen of gefitinib combined with bevacizumab. This combination was well tolerated and resulted in a partial response, achieving a progression-free survival (PFS) of 15.5 months. Conclusion: This case indicates that the combination of gefitinib and bevacizumab may offer a durable clinical benefit for NSCLC patients who develop Osimertinib resistance via the C797S mutation. The observed outcomes warrant further investigation into this dual-blockade strategy, especially given the limited duration of response noted for tyrosine kinase inhibitor (TKI) monotherapy.

Keywords: non-small-cell lung cancer, epidermal growth factor receptor, C797S mutation, tyrosine kinase inhibitor, bevacizumab

Received: 26 Jul 2025; Accepted: 23 Sep 2025.

Copyright: © 2025 Tan, Dong, Li, Li, Xiong, Bao, Dai, Yue and Liu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Yuan Liu, liu_yuan2000@sina.com

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