Olmutinib in T790M-positive non-small cell lung cancer after failure of first-line epidermal growth factor receptor-tyrosine kinase inhibitor therapy: A global, phase 2 study

被引:23
作者
Park, Keunchil [1 ]
Janne, Pasi A. [2 ]
Kim, Dong-Wan [3 ]
Han, Ji-Youn [4 ]
Wu, Ming-Fang [5 ]
Lee, Jong-Seok [6 ]
Kang, Jin-Hyoung [7 ]
Lee, Dae Ho [8 ]
Cho, Byoung Chul [9 ]
Yu, Chong-Jen [10 ]
Pang, Yong Kek [11 ]
Felip, Enriqueta [12 ]
Kim, Hyunjin [13 ]
Baek, Eunhye [13 ]
Noh, Young Su [13 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Div Hematol Oncol, Seoul, South Korea
[2] Dana Farber Canc Inst, Lowe Ctr Thorac Oncol, Belfer Inst Appl Canc Sci, Boston, MA 02115 USA
[3] Seoul Natl Univ Hosp, Dept Internal Med, Seoul, South Korea
[4] Natl Canc Ctr, Goyang, South Korea
[5] Chung Shan Med Univ Hosp, Taichung, Taiwan
[6] Seoul Natl Univ, Bundang Hosp, Div Hematol & Med Oncol, Dept Internal Med, Seongnam, South Korea
[7] Catholic Univ Korea, Seoul St Marys Hosp, Dept Radiat Oncol, Seoul, South Korea
[8] Univ Ulsan, Dept Oncol, Coll Med, Asan Med Ctr, Seoul, South Korea
[9] Yonsei Univ, Yonsei Canc Ctr, Coll Med, Seoul, South Korea
[10] Natl Taiwan Univ Hosp, Internal Med, Taipei, Taiwan
[11] Univ Malaya, Med Ctr, Div Resp Med, Kuala Lumpur, Malaysia
[12] Vall dHebron Inst Oncol, Vall dHebron Univ Hosp, Med Oncol, Barcelona, Spain
[13] Hanmi Pharmaceut Co Ltd, Seoul, South Korea
关键词
epidermal growth factor receptor; non-small cell lung cancer; olmutinib; T790M; tyrosine kinase inhibitor; ACQUIRED-RESISTANCE; II TRIAL; EGFR; GEFITINIB; ERLOTINIB; CHEMOTHERAPY; AFATINIB; MUTATION; OSIMERTINIB; CARBOPLATIN;
D O I
10.1002/cncr.33385
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: In this open-label, international phase 2 study, the authors assessed the efficacy and safety of olmutinib in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) who had a confirmed T790M mutation and disease progression on previous epidermal growth factor receptor-tyrosine kinase inhibitor therapy. METHODS: Patients aged >= 20 years received once-daily oral olmutinib 800 mg continuously in 21-day cycles. The primary endpoint was the objective response rate (patients who had a confirmed best overall response of a complete or partial response), assessed by central review. Secondary endpoints included the disease control rate, the duration of objective response, progression-free survival, and overall survival. Adverse events were graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (version 4.03). RESULTS: Overall, 162 patients (median age, 63 years; women, >60%) were enrolled from 68 sites in 9 countries. At the time of database cutoff, 23.5% of enrolled patients remained on treatment. The median treatment duration was 6.5 months (range, 0.03-21.68 months). Overall, 46.3% of patients (95% CI, 38.4%-54.3%) had a confirmed objective response (all partial responses). The best overall response (the objective response rate regardless of confirmation) was 51.9% (84 patients; 95% CI, 43.9%-59.8%). The confirmed disease control rate for all patients was 86.4% ( 95% CI, 80.2%-91.3%). The median duration of objective response was 12.7 months (95% CI, 8.3-15.4 months). Estimated median progression-free survival was 9.4 months (95% CI, 6.9-12.3 months), and estimated median overall survival was 19.7 months (95% CI, 15.1 months to not reached). All patients experienced treatment-emergent adverse events, and 71.6% of patients had grade >= 3 treatment-emergent adverse events. CONCLUSIONS: Olmutinib has meaningful clinical activity and a manageable safety profile in patients with T790M-positive non-small cell lung cancer who received previous epidermal growth factor receptor-tyrosine kinase inhibitor therapy. Cancer 2020;0:1-10. (c) 2020 The Authors. Cancer published by Wiley Periodicals LLC on behalf of American Cancer Society. This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
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页码:1407 / 1416
页数:10
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