Switching from first or second generation EGFR-TKI to osimertinib in EGFR mutation-positive NSCLC

被引:8
|
作者
Imamura, Fumio [1 ]
Inoue, Takako [1 ]
Kunimasa, Kei [1 ]
Kubota, Aki [2 ]
Kuhara, Hanako [1 ]
Tamiya, Motohiro [1 ]
Nishino, Kazumi [1 ]
Kimura, Madoka [1 ]
Kuno, Kika [1 ]
Kawachi, Hayato [1 ]
Kumagai, Toru [1 ]
机构
[1] Osaka Int Canc Inst, Dept Thorac Oncol, Chio Ku, 3-1-69 Otemae, Osaka 5418567, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Biomed Stat & Bioinformat, Sakyo Ku, 54 Kawaharacho, Kyoto 6068507, Japan
关键词
EGFR-TKI; EGFR mutation; NSCLC; osimertinib; switch; time to failure of strategy; CELL LUNG-CANCER; 1ST-LINE TREATMENT; OPEN-LABEL; CLINICAL IMPACT; TUMOR-CELLS; END-POINTS; AFATINIB; ADENOCARCINOMA; FEASIBILITY; PROGRESSION;
D O I
10.2217/lmt-2020-0005
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Aim: We evaluated the efficacy of a novel switch protocol for EGFR-TKIs for EGFR mutation-positive NSCLC. Materials & methods: Clinical records were collected from the patients who had received one of two sequential combination strategies of EGFR-TKIs: Salvage use of osimertinib for T790M-mediated acquired resistance to an prior EGFR-TKI or switch use of osimertinib where an EGFR-TKI was switched to osimertinib before disease progression. Results: Progression-free survival of osimertinib and time from the start of treatment until progression to osimertinib was comparable between the salvage use and switch use of osimertinib. Conclusion: Switch use of osimertinib seemed to produce improved efficacy for patients with activating EGFR mutations, because of the lack of patient selection via T790M.
引用
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页数:8
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