CASE REPORT article
Front. Oncol.
Sec. Cancer Molecular Targets and Therapeutics
Case Report:furmonertinib dose escalation in heavily pretreated EGFR-mutant lung adenocarcinoma with diffuse brain metastases
Zian Jin
Changhong Dong
Kaiyuan Hui
Xiaodong Jiang
The Affiliated Lianyungang Hospital of Xuzhou Medical University, Lianyungang, China
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Abstract
Furmonertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, has demonstrated systemic and central nervous system (CNS) antitumor activity in patients with EGFR-mutant non-small cell lung cancer (NSCLC); however, evidence supporting its use in patients with diffuse brain metastases after multiple lines of therapy and very poor performance status remains limited. Here, we report the case of a 53-year-old man with EGFR L858R-mutant stage IV lung adenocarcinoma who developed multifocal progression involving the lungs, liver, bones, and brain after multiple prior treatments. At admission, he had diffuse brain metastases and an Eastern Cooperative Oncology Group (ECOG) performance status of 4, and he was unable to undergo whole-brain radiotherapy because of impaired consciousness. Dose-escalated furmonertinib was initiated and led to marked relief of neurological and respiratory symptoms within a few days. Subsequent imaging assessments showed sustained clinical benefit, with improvement in performance status and activities of daily living. This case suggests that, in EGFR-mutant advanced NSCLC with extensive CNS progression after multiline treatment failure in whom radiotherapy is not feasible, high-dose furmonertinib may represent a potential salvage option and may help inform individualized treatment strategies in this high-risk population. This single case is hypothesis-generating and larger cohorts/prospective studies are needed to confirm efficacy, safety, and appropriate patient selection.
Summary
Keywords
diffuse brain metastases, Dose Escalation, EGFR L858R mutation, furmonertinib, Non-small cell lung cancer
Received
06 January 2026
Accepted
17 February 2026
Copyright
© 2026 Jin, Dong, Hui and Jiang. 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: Kaiyuan Hui; Xiaodong Jiang
Disclaimer
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