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Successful Treatment with Ramucirumab Plus Erlotinib following Osimertinib-induced Interstitial Lung Disease
Shodai Fujimoto1, Naoko Katsurada1, Daisuke Hazama1
1Division of Respiratory Medicine, Department of Internal Medicine, Kobe University Graduate School of Medicine, Japan.
Abstract:
Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) are key drugs for patients with EGFR mutation-positive non-small cell lung cancer, and osimertinib is the standard treatment. Although drug-induced interstitial lung disease (ILD) is a remarkable adverse event of EGFR-TKIs, evidence regarding the continuation and re-challenge of EGFR-TKIs after drug-induced severe ILD is lacking. This is the first report of successful switching to ramucirumab plus erlotinib after osimertinib-induced severe ILD in an 81-year-old woman with stage IV lung adenocarcinoma harboring the EGFR L858R mutation in exon 21. These findings suggest that ramucirumab plus erlotinib may be a viable treatment option for osimertinib-induced severe ILD.
Insights
Osimertinib can cause severe interstitial lung disease (ILD) in non-small cell lung cancer patients. Switching to ramucirumab plus erlotinib offers a potential treatment option for patients experiencing this adverse event.
Area of Science:
- Oncology
- Pulmonology
- Pharmacology
Background:
- Epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) are crucial for EGFR mutation-positive non-small cell lung cancer (NSCLC).
- Osimertinib is a standard EGFR-TKI, but drug-induced interstitial lung disease (ILD) is a significant adverse event.
- Limited evidence exists on continuing or re-challenging EGFR-TKIs after severe drug-induced ILD.
Purpose of the Study:
- To report the first successful treatment switch in a patient with osimertinib-induced severe ILD.
- To evaluate ramucirumab plus erlotinib as a potential alternative therapy post-osimertinib-induced severe ILD.
Main Methods:
- Case report of an 81-year-old woman with stage IV lung adenocarcinoma and EGFR L858R mutation.
- Patient experienced severe ILD while on osimertinib treatment.
- Treatment was switched to ramucirumab plus erlotinib.
Main Results:
- Successful treatment continuation with ramucirumab plus erlotinib after osimertinib-induced severe ILD.
- The patient tolerated the new regimen, suggesting its viability.
Conclusions:
- Ramucirumab plus erlotinib may be a viable treatment option for patients with severe ILD induced by osimertinib.
- This finding provides valuable insight into managing severe adverse events in NSCLC treatment.
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