Osimertinib in Pretreated T790M-Positive Advanced Non-Small-Cell Lung Cancer: AURA Study Phase II Extension Component

被引:473
|
作者
Yang, James Chih-Hsin [1 ]
Ahn, Myung-Ju [3 ]
Kim, Dong-Wan [4 ]
Ramalingam, Suresh S. [7 ]
Sequist, Lecia V. [8 ]
Su, Wu-Chou [2 ]
Kim, Sang-We [5 ]
Kim, Joo-Hang [6 ]
Planchard, David [10 ]
Felip, Enriqueta [11 ]
Blackhall, Fiona [12 ]
Haggstrom, Daniel [15 ]
Yoh, Kiyotaka [16 ]
Novello, Silvia [18 ]
Gold, Kathryn [19 ]
Hirashima, Tomonori [17 ]
Lin, Chia-Chi [1 ]
Mann, Helen [13 ]
Cantarini, Mireille [14 ]
Ghiorghiu, Serban [13 ]
Janne, Pasi A. [9 ]
机构
[1] Natl Taiwan Univ Hosp, Taipei, Taiwan
[2] Natl Cheng Kung Univ Hosp, Tainan, Taiwan
[3] Sungkyunkwan Univ, Seoul, South Korea
[4] Seoul Natl Univ Hosp, Seoul, South Korea
[5] Asan Med Ctr, Seoul, South Korea
[6] CHA Univ, Gyeonggi Do, South Korea
[7] Emory Univ, Sch Med, Atlanta, GA USA
[8] Massachusetts Gen Hosp, Boston, MA 02114 USA
[9] Dana Farber Canc Inst, Boston, MA 02115 USA
[10] Inst Gustave Roussy, Villejuif, France
[11] Vall dHebron Univ Hosp, Barcelona, Spain
[12] Univ Manchester, Christie Hosp, Manchester, Lancs, England
[13] AstraZeneca, Cambridge, England
[14] AstraZeneca, Macclesfield, Cheshire, England
[15] Carolinas Healthcare Syst, Charlotte, NC USA
[16] Natl Canc Ctr Hosp East, Kashiwa, Chiba, Japan
[17] Osaka Prefectural Med Ctr Resp & Allerg Dis, Osaka, Japan
[18] Univ Turin, Turin, Italy
[19] Univ Calif San Diego, Moores Canc Ctr, San Diego, CA 92103 USA
关键词
GROWTH-FACTOR RECEPTOR; OPEN-LABEL; 1ST-LINE TREATMENT; ACQUIRED-RESISTANCE; EGFR MUTATIONS; CHEMOTHERAPY; GEFITINIB; MULTICENTER; AFATINIB; INHIBITORS;
D O I
10.1200/JCO.2016.70.3223
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Osimertinib is an irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) selective for both EGFR-TKI sensitizing (EGFRm) and T790M resistance mutations. AURA (NCT01802632) is a phase I/II clinical trial to determine the dose, safety, and efficacy of osimertinib. This article reports the results from the phase II extension component. Patients and Methods Patients with EGFR-TKI-pretreated EGFRm- and T790M-positive advanced non-small-cell lung cancer (NSCLC) received once-daily osimertinib 80 mg. T790M status was confirmed by central testing from a tumor sample taken after the most recent disease progression. Patients with asymptomatic, stable CNS metastases that did not require corticosteroids were allowed to enroll. The primary end point was objective response rate (ORR) by independent radiology assessment. Secondary end points were disease control rate, duration of response, progression-free survival (PFS), and safety. Patient-reported outcomes comprised an exploratory objective. Results In total, 201 patients received treatment, with a median treatment duration of 13.2 months at the time of data cutoff (November 1, 2015). In evaluable patients (n = 198), ORR was 62% (95% CI, 54% to 68%), and the disease control rate was 90% (95% CI, 85 to 94). Median duration of response in 122 responding patients was 15.2 months (95% CI, 11.3 to not calculable). Median PFS was 12.3 months (95% CI, 9.5 to 13.8). The most common possibly causally related adverse events (investigator assessed) were diarrhea (43%; grade >= 3, <1%) and rash (grouped terms; 40%; grade >= 3, <1%). Interstitial lung disease (grouped terms) was reported in eight patients (4%; grade 1, n = 2; grade 3, n = 3; grade 5, n = 3). Conclusion In patients with EGFRm T790M advanced NSCLC who progress after EGFR-TKI treatment, osimertinib provides a high ORR, encouraging PFS, and durable response. (C) 2017 by American Society of Clinical Oncology
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页码:1288 / +
页数:16
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