Osimertinib versus standard-of-care EGFR-TKI as first-line treatment for EGFRm advanced NSCLC: FLAURA Japanese subset

被引:141
作者
Ohe, Yuichiro [1 ]
Imamura, Fumio [2 ]
Nogami, Naoyuki [3 ]
Okamoto, Isamu [4 ]
Kurata, Takayasu [5 ]
Kato, Terufumi [6 ]
Sugawara, Shunichi [7 ]
Ramalingam, Suresh S. [8 ]
Uchida, Hirohiko [9 ]
Hodge, Rachel [10 ]
Vowler, Sarah L. [10 ]
Walding, Andrew [10 ]
Nakagawa, Kazuhiko [11 ]
机构
[1] Natl Canc Ctr, Dept Thorac Oncol, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[2] Osaka Int Canc Inst, Dept Thorac Oncol, Chuo Ku, Osaka, Japan
[3] Natl Hosp Org Shikoku Canc Ctr, Dept Thorac Oncol, Minamiumemoto Machi, Matsuyama, Ehime, Japan
[4] Kyushu Univ, Grad Sch Med Sci, Res Inst Dis Chest, Higashi Ku, Fukuoka, Fukuoka, Japan
[5] Kansai Med Univ Hosp, Dept Thorac Oncol, Hirakata, Osaka, Japan
[6] Kanagawa Cardiovasc & Resp Ctr, Dept Resp Med, Kanazawa Ku, Yokohama, Kanagawa, Japan
[7] Sendai Kousei Hosp, Dept Pulm Med, Aoba Ku, Sendai, Miyagi, Japan
[8] Emory Univ, Winship Canc Ctr, Atlanta, GA 30322 USA
[9] AstraZeneca KK, Res & Dev, Kita Ku, Grand Front Osaka Tower B, Osaka, Japan
[10] AstraZeneca, da Vinci Bldg,Melbourn Sci Pk, Melbourn, Cambs, England
[11] Kindai Univ Hosp, Dept Med Oncol, Osaka, Japan
关键词
clinical trials; lung medicine; thoracic; CELL LUNG-CANCER; OPEN-LABEL; MUTATION; THERAPY; RESISTANCE; GEFITINIB; AFATINIB; DISEASE;
D O I
10.1093/jjco/hyy179
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The FLAURA study was a multicenter, double-blind, Phase 3 study in which patients with previously untreated epidermal growth factor receptor mutation-positive advanced non-small-cell lung carcinoma were randomized 1:1 to oral osimertinib 80 mg once daily or standard-of-care (gefitinib 250 mg or erlotinib 150 mg, once daily) to compare safety and efficacy. In the overall FLAURA study, significantly better progression-free survival was shown with osimertinib versus standard-of-care. Methods: Selected endpoints, including progression-free survival (primary endpoint), overall survival, objective response rate, duration of response and safety were evaluated for the Japanese subset of the FLAURA study. Results: In Japan, 120 eligible Japanese patients were randomized to osimertinib (65 patients) or gefitinib (55 patients) treatment from December 2014 to June 2017. Median progression-free survival was 19.1 (95% confidence interval, 12.6, 23.5) and 13.8 (95% confidence interval, 8.3, 16.6) months with osimertinib and gefitinib, respectively (hazard ratio, 0.61; 95% confidence interval, 0.38, 0.99). Median overall survival was not reached in either treatment arm (data were immature). In the osimertinib and gefitinib arms, objective response rate was 75.4% (49/65) and 76.4% (42/55), and median duration of response from onset was 18.4 (95% confidence interval, not calculated) and 9.5 (95% confidence interval, 6.2, 13.9) months, respectively. The incidence of adverse events was similar in the two groups. The frequency of Grade >= 3 interstitial lung disease and pneumonitis in the two groups were the same (one patient). Conclusions: As the first-line therapy, osimertinib showed significantly improved efficacy versus gefitinib in the Japanese population of the FLAURA study. No new safety concerns were raised.
引用
收藏
页码:29 / 36
页数:8
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