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First case report of erlotinib plus ramucirumab treatment for lung carcinosarcoma with EGFR L858R mutation

Lung carcinosarcoma is acknowledged as a rare form of lung cancer. Due to its rarity, the inability to conduct large‐scale clinical trials and interventions is currently carried out based on empirical evidence. In this study, we report the case of a 73‐year‐old female patient diagnosed with postoper...

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Detalles Bibliográficos
Autores principales: Ishibashi, Naoya, Tabata, Toshiharu, Nonomura, Ryo, Oshima, Yutaka, Sasaki, Takanobu, Mitomo, Hideki, Sugawara, Takafumi, Sagawa, Motoyasu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693942/
https://www.ncbi.nlm.nih.gov/pubmed/37837329
http://dx.doi.org/10.1111/1759-7714.15134
Descripción
Sumario:Lung carcinosarcoma is acknowledged as a rare form of lung cancer. Due to its rarity, the inability to conduct large‐scale clinical trials and interventions is currently carried out based on empirical evidence. In this study, we report the case of a 73‐year‐old female patient diagnosed with postoperative recurrence of lung carcinosarcoma. The resected tumor was diagnosed as lung carcinosarcoma, and genetic testing revealed the presence of the epidermal growth factor receptor (EGFR) exon21 L858R. Approximately 2 years postoperatively, the tumor recurred and the patient was treated with erlotinib plus ramucirumab, which were effective in controlling metastatic disease. Erlotinib plus ramucirumab is therefore a treatment option for EGFR mutation‐positive lung carcinosarcoma.