Case Report: Furmonertinib-induced acute interstitial lung disease

Furmonertinib is a third-generation irreversible epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that selectively inhibits EGFR-TKI-sensitive mutations. Although furmonertinib is generally well-tolerated and no severe drug-related interstitial lung disease (ILD) has been reported in the literature to date, we present a case of furmonertinib-induced ILD in a 71-year-old woman with EGFR-mutated lung adenocarcinoma (LUAD). On day 97 of treatment, the patient developed acute severe dyspnea, which rapidly progressed to diffuse bilateral lung consolidation and profound hypoxemia. After excluding other potential causes of interstitial pneumonia, a diagnosis of furmonertinib-related ILD was established. Through timely diagnosis and appropriate intervention, the patient achieved a favorable outcome. This case highlights that early recognition and management can reverse this serious adverse event and help preserve subsequent treatment options.

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Publication Details

Journal
Frontiers in Pharmacology
Published
2026-01-08
DOI
https://doi.org/10.3389/fphar.2025.1742670
Primary Topic
Lung Cancer Treatments and Mutations
Type
article
Field-Weighted Citation Impact
0.00

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article

Case Report: Furmonertinib-induced acute interstitial lung disease

Wang Di-ming, Mingfeng Han, Y. Fred Yang, Yong-liang Niu et al.
Frontiers in Pharmacology
Lung Cancer Treatments and Mutations
article

Case Report: Furmonertinib-induced acute interstitial lung disease

Wang Di-ming, Mingfeng Han, Y. Fred Yang, Yong-liang Niu, Jing-feng Shi
article en

Abstract

Furmonertinib is a third-generation irreversible epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) that selectively inhibits EGFR-TKI-sensitive mutations. Although furmonertinib is generally well-tolerated and no severe drug-related interstitial lung disease (ILD) has been reported in the literature to date, we present a case of furmonertinib-induced ILD in a 71-year-old woman with EGFR-mutated lung adenocarcinoma (LUAD). On day 97 of treatment, the patient developed acute severe dyspnea, which rapidly progressed to diffuse bilateral lung consolidation and profound hypoxemia. After excluding other potential causes of interstitial pneumonia, a diagnosis of furmonertinib-related ILD was established. Through timely diagnosis and appropriate intervention, the patient achieved a favorable outcome. This case highlights that early recognition and management can reverse this serious adverse event and help preserve subsequent treatment options.

Frontiers in PharmacologyVol. 16
Shanghai Jiao Tong University (CN), Shanghai Chest Hospital (CN), Fuyang City People's Hospital (CN), Xi'an Chest Hospital (CN)
National Natural Science Foundation of China
Good health and well-being
Openalex Percentile: Top 97%
Lung Cancer Treatments and Mutations
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