Real-world osimertinib for EGFR mutation-positive non-small-cell lung cancer with acquired T790M mutation

被引:8
|
作者
Imamura, Fumio [1 ]
Kimura, Madoka [1 ]
Yano, Yukihiro [2 ]
Mori, Masahide [2 ]
Suzuki, Hidekazu [3 ]
Hirashima, Tomonori [3 ]
Ihara, Shouichi [4 ]
Komuta, Kiyoshi [4 ]
Shiroyama, Takayuki [5 ]
Nagatomo, Izumi [5 ]
Kumagai, Toru [1 ]
机构
[1] Osaka Int Canc Inst, Dept Thorac Oncol, Chuo Ku, 3-1-69 Otemae, Osaka 5418567, Japan
[2] Natl Hosp Org Osaka Toneyama Med Ctr, Dept Thorac Oncol, 5-1-1 Toneyama, Toyonaka, Osaka 5608552, Japan
[3] Osaka Habikino Med Ctr, Dept Thorac Oncol, 3-7-1 Habikino, Habikino, Osaka 5838588, Japan
[4] Osaka Police Hosp, Dept Respirol, Tenoji Ku, 2-6-40 Karasugatsuji, Osaka 5438922, Japan
[5] Osaka Univ, Grad Sch Med, Dept Resp Med & Clin Immunol, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan
关键词
1ST-LINE TREATMENT; OPEN-LABEL; GEFITINIB;
D O I
10.2217/fon-2020-0203
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: Osimertinib is a key drug for EGFR mutation-positive non-small-cell lung cancer (NSCLC). As the hazards ratio of overall survival in comparison with first-generation EGFR-tyrosine kinase inhibitors was almost similar between FLAURA and ARCHER 1050, salvage use of osimertinib is still a treatment option. Patients & methods: We retrospectively analyzed the clinical courses of EGFR mutation-positive NSCLC patients who were potential candidates for salvage osimertinib. Results: Among 524 patients enrolled from five hospitals, 302 patients underwent biopsy, with 52.6% detection rate of T790M. Osimertinib was administered in 93.6% of the T790M-positive patients. The overall response rate and median progression-free survival time of osimertinib were calculated with 147 patients, to be 55.6% and 17.2 months, respectively. Conclusion: Osimertinib is active for T790M-driven acquired resistance in EGFR-mutant NSCLC, but the detection of T790M was unsatisfactory.
引用
收藏
页码:1537 / 1546
页数:10
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