ArticleFrontiers in oncology2025
Case report: Anlotinib plus oral etoposide: a potential salvage therapy based on insights from EGFR-TKI-resistant SCLC transformation PDX and clinical settings.
Article in Frontiers in oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Small cell lung cancer (SCLC) transformation is one of the resistance mechanisms to epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) treatment in patients with lung adenocarcinoma (LUAD). Platinum-etoposide chemotherapy is the most common regimen for patients with SCLC transformation. Despite a high initial response rate, patients experience rapid disease progression, and there is a paucity of evidence for further-line therapy. In this study, we report two cases of patients with EGFR 19del-mutated and EGFR-TKI-resistant transformed SCLC who failed with platinum-etoposide chemotherapy. We explored a novel combination strategy of anlotinib and orally administered etoposide in these two patients, guided by the results of a patient-derived tumor xenograft (PDX) model. The combination regimen was clinically applied when platinum-etoposide chemotherapy failed, and both patients benefited from the treatment. To our knowledge, this is the first report of anlotinib plus oral etoposide as a potential salvage therapy for patients with EGFR-TKI-induced SCLC transformation resistant to platinum-based chemotherapy. Both the PDX model and clinical cases support the efficacy of this regimen, providing a promising therapeutic option for patients with SCLC transformation after platinum-etoposide chemotherapy resistance.
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