Document Type
Report
Publication Date
10-17-2025
Abstract
Regorafenib-induced pneumonitis and acute respiratory distress syndrome (ARDS) are rare and poorly characterized toxicities. We describe a 43-year-old male with metastatic colorectal cancer who developed hypoxic respiratory failure after two cycles of regorafenib. Imaging revealed cavitary lung lesions and diffuse ground glass opacities. Despite antibiotics and high-dose corticosteroids, his condition deteriorated, requiring ICU admission and mechanical ventilation. Bronchoalveolar lavage revealed bacterial pathogens, and he was treated for pneumonia. After multidisciplinary discussion, he was assessed to have regorafenib-induced pneumonitis as a major driver of his respiratory failure, and after limited steroid response, infliximab was administered with marked respiratory improvement. However, he later developed fungal sepsis and died from refractory shock. This is the first reported case of regorafenib-induced pneumonitis and ARDS treated with infliximab and corticosteroids. The patient's transient response suggests overlap with immune-related pneumonitis mechanisms seen in tyrosine kinase and immune checkpoint inhibitor therapies. Further research is needed to clarify regorafenib's immunotoxicity and the role of advanced immunosuppressive therapies in managing pneumonitis.
Recommended Citation
Dong, Michael; Kramer, Mackenzie; Gandhi, Tanmay; and George, Gautam, "Regorafenib Pulmonary Toxicity: A Case of Cavitary Lung Disease and ARDS Treated With Infliximab" (2025). Division of Pulmonary, Allergy, and Critical Care Medicine Faculty Papers. Paper 53.
https://jdc.jefferson.edu/pulmcritcarefp/53
Creative Commons License

This work is licensed under a Creative Commons Attribution-Noncommercial 4.0 License
PubMed ID
41210153
Language
English
Included in
Chemical and Pharmacologic Phenomena Commons, Chemicals and Drugs Commons, Pulmonology Commons, Respiratory Tract Diseases Commons


Comments
This article is the author’s final published version in Respiratory Medicine Case Reports, Volume 58, 2025, Article number 102302.
The published version is available at https://doi.org/10.1016/j.rmcr.2025.102302. Copyright © 2025 The Authors.