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학술저널
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Kim, Eun-Young (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Kim, Yoon-Hee (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Ban, Hee-Jung (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Oh, In-Jae (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Kwon, Yong-Soo (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Kim, Kyu-Sik (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Kim, Yu-Il (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Lim, Sung-Chul (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital) Kim, Young-Chul (Lung and Esophageal Cancer Clinic, Chonnam National University Hwasun Hospital)
저널정보
대한결핵 및 호흡기학회 Tuberculosis and Respiratory Diseases 결핵 및 호흡기 질환 제74권 제3호
발행연도
2013.1
수록면
129 - 133 (5page)

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The presence of epidermal growth factor receptor (EGFR ) mutation is a prognostic and predictive marker for EGFR-tyrosine kinase inhibitor (TKI) therapy. However, inevitably, relapse occurs due to the development of acquired resistance, such as T790M mutation. We report a case of repeated responses to EGFR-TKIs in a never-smoked woman with adenocarcinoma. After six cycles of gemcitabine and cisplatin, the patient was treated by gefitinib for 4 months until progression. Following the six cycles of third-line pemetrexed, gefitinib retreatment was initiated and continued with a partial response for 6 months. After progression, she was recruited for an irreversible EGFR inhibitor trial, and the time to progression was 11 months. Although EGFR direct sequencing on the initial diagnostic specimen revealed a wild-type, we performed a rebiopsy from the progressed subcarinal node at the end of the trial. The result of peptide nucleic acid clamping showed L858R/L861Q.

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