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Pembrolizumab and salvage chemotherapy in EGFR T790M-positive non-small-cell lung cancer with high PD-L1 expression

Immuno-checkpoint inhibitors (ICI) have become an effective treatment option for non-small-cell lung cancer patients. However, ICI therapy was reported to be less effective in patients with epidermal growth factor receptor (EGFR) mutations than in those with wild-type EGFR. We report here that an no...

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Detalles Bibliográficos
Autores principales: Tozuka, Takehiro, Seike, Masahiro, Minegishi, Yuji, Kitagawa, Shingo, Kato, Tomomi, Takano, Natsuki, Hisakane, Kakeru, Takahashi, Satoshi, Kobayashi, Kenichi, Kashiwada, Takeru, Sugano, Teppei, Takeuchi, Susumu, Kunugi, Shinobu, Noro, Rintaro, Saito, Yoshinobu, Kubota, Kaoru, Gemma, Akihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6135433/
https://www.ncbi.nlm.nih.gov/pubmed/30237726
http://dx.doi.org/10.2147/OTT.S168598
Descripción
Sumario:Immuno-checkpoint inhibitors (ICI) have become an effective treatment option for non-small-cell lung cancer patients. However, ICI therapy was reported to be less effective in patients with epidermal growth factor receptor (EGFR) mutations than in those with wild-type EGFR. We report here that an non-small-cell lung cancer patient with the EGFR mutant T790M showed a programmed cell death ligand 1 (PD-L1) expression level that increased from <25% to >90% after eighth-line osimertinib therapy. He was treated with pembrolizumab as a ninth-line treatment, and attained stable disease. After the pembrolizumab therapy, he was treated with gemcitabine, which produced a good response despite being the 10th-line treatment. We should consider administering ICI and chemotherapy even to EGFR mutant patients after failure of EGFR tyrosine kinase inhibitor, especially in cases with high PD-LI expression.