CNS Efficacy of Osimertinib in Patients With T790M-Positive Advanced Non-Small-Cell Lung Cancer: Data From a Randomized Phase III Trial (AURA3)

被引:409
作者
Wu, Yi-Long [1 ,2 ]
Ahn, Myung-Ju [3 ]
Garassino, Marina Chiara [6 ]
Han, Ji-Youn [5 ]
Katakami, Nobuyuki [7 ]
Kim, Hye Ryun [4 ]
Hodge, Rachel [8 ]
Kaur, Paramjit [8 ]
Brown, Andrew P. [8 ]
Ghiorghiu, Dana [8 ]
Papadimitrakopoulou, Vassiliki A. [9 ]
Mok, Tony S. K. [10 ]
机构
[1] Guangdong Acad Med Sci, 106 Zhongshan Er Rd, Guangzhou 510080, Guangdong, Peoples R China
[2] Guangdong Gen Hosp, Guangzhou, Guangdong, Peoples R China
[3] Sungkyunkwan Univ, Sch Med, Seoul, South Korea
[4] Yonsei Univ, Coll Med, Seoul, South Korea
[5] Natl Canc Ctr, Goyang, South Korea
[6] Fdn IRCCS Ist Nazl Tumori, Milan, Italy
[7] Inst Biomed Res & Innovat, Kobe, Hyogo, Japan
[8] AstraZeneca, Cambridge, England
[9] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[10] Chinese Univ Hong Kong, Hong Kong, Hong Kong, Peoples R China
关键词
BLOOD-BRAIN-BARRIER; TYROSINE KINASE INHIBITOR; ACQUIRED-RESISTANCE; OPEN-LABEL; EGFR-TKIS; METASTASES; GEFITINIB; PERMEABILITY; MULTICENTER;
D O I
10.1200/JCO.2018.77.9363
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeIn patients with epidermal growth factor receptor (EGFR) mutation-positive advanced non-small-cell lung cancer (NSCLC), there is an unmet need for EGFR-tyrosine kinase inhibitors with improved CNS penetration and activity against CNS metastases, either at initial diagnosis or time of progression. We report the first comparative evidence of osimertinib CNS efficacy versus platinum-pemetrexed from a phase III study (AURA3; ClinicalTrials.gov identifier: NCT02151981) in patients with EGFR T790M-positive advanced NSCLC who experience disease progression with prior EGFR-tyrosine kinase inhibitor treatment.MethodsPatients with asymptomatic, stable CNS metastases were eligible for enrollment and were randomly assigned 2:1 to osimertinib 80 mg once daily or platinum-pemetrexed. A preplanned subgroup analysis was conducted in patients with measurable and/or nonmeasurable CNS lesions on baseline brain scan by blinded independent central neuroradiological review. The CNS evaluable for response set included only patients with one or more measurable CNS lesions. The primary objective for this analysis was CNS objective response rate (ORR).ResultsOf 419 patients randomly assigned to treatment, 116 had measurable and/or nonmeasurable CNS lesions, including 46 patients with measurable CNS lesions. At data cutoff (April 15, 2016), CNS ORR in patients with one or more measurable CNS lesions was 70% (21 of 30; 95% CI, 51% to 85%) with osimertinib and 31% (5 of 16; 95% CI, 11% to 59%) with platinum-pemetrexed (odds ratio, 5.13; 95% CI, 1.44 to 20.64; P = .015); the ORR was 40% (30 of 75; 95% CI, 29% to 52%) and 17% (7 of 41; 95% CI, 7% to 32%), respectively, in patients with measurable and/or nonmeasurable CNS lesions (odds ratio, 3.24; 95% CI, 1.33 to 8.81; P = .014). Median CNS duration of response in patients with measurable and/or nonmeasurable CNS lesions was 8.9 months (95% CI, 4.3 months to not calculable) for osimertinib and 5.7 months (95% CI, 4.4 to 5.7 months) for platinum-pemetrexed; median CNS progression-free survival was 11.7 months and 5.6 months, respectively (hazard ratio, 0.32; 95% CI, 0.15 to 0.69; P = .004).ConclusionOsimertinib demonstrated superior CNS efficacy versus platinum-pemetrexed in T790M-positive advanced NSCLC.
引用
收藏
页码:2702 / +
页数:10
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