Brigatinib in Patients With Alectinib-Refractory ALK-Positive NSCLC

被引:63
|
作者
Lin, Jessica J. [1 ]
Zhu, Viola W. [2 ]
Schoenfeld, Adam J. [3 ]
Yeap, Beow Y. [1 ]
Saxena, Ashish [4 ]
Ferris, Lorin A. [1 ]
Dagogo-Jack, Ibiayi [1 ]
Farago, Anna F. [1 ]
Taber, Angela [5 ]
Traynor, Anne [6 ]
Menon, Smitha [7 ]
Gainor, Justin F. [1 ]
Lennerz, Jochen K. [8 ]
Plodkowski, Andrew J. [9 ]
Digumarthy, Subba R. [10 ]
Ignatius, Sai-Hong [2 ]
Shaw, Alice T. [1 ]
Riely, Gregory J. [3 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[2] Univ Calif Irvine, Sch Med, Chao Family Comprehens Canc Ctr, Orange, CA 92668 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med, 1275 York Ave, New York, NY 10021 USA
[4] Weill Cornell Med, Dept Med, New York, NY USA
[5] Lifespan Canc Inst, Providence, RI USA
[6] Univ Wisconsin, Dept Med, Carbone Canc Ctr, Madison, WI USA
[7] Med Coll Wisconsin, Dept Med, Milwaukee, WI 53226 USA
[8] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[9] Mem Sloan Kettering Canc Ctr, Dept Radiol, 1275 York Ave, New York, NY 10021 USA
[10] Massachusetts Gen Hosp, Dept Radiol, Boston, MA USA
关键词
Alectinib; Brigatinib; ALK; NSCLC; Resistance; CELL LUNG-CANCER; OPEN-LABEL; SINGLE-ARM; CRIZOTINIB; CHEMOTHERAPY; CERITINIB; LORLATINIB; PHASE-2;
D O I
10.1016/j.jtho.2018.06.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: The second-generation anaplastic lymphoma kinase (ALK) inhibitor alectinib recently showed superior efficacy compared to the first-generation ALK inhibitor crizotinib in advanced ALK-rearranged NSCLC, establishing alectinib as the new standard first-line therapy. Brigatinib, another second-generation ALK inhibitor, has shown substantial activity in patients with crizotinib-refractory ALK-positive NSCLC; however, its activity in the alectinib-refractory setting is unknown. Methods: A multicenter, retrospective study was performed at three institutions. Patients were eligible if they had advanced, alectinib-refractory ALK-positive NSCLC and were treated with brigatinib. Medical records were reviewed to determine clinical outcomes. Results: Twenty-two patients were eligible for this study. Confirmed objective responses to brigatinib were observed in 3 of 18 patients (17%) with measurable disease. Nine patients (50%) had stable disease on brigatinib. The median progression-free survival was 4.4 months (95% confidence interval [CI]: 1.8-5.6 months) with a median duration of treatment of 5.7 months (95% CI: 1.8-6.2 months). Among 9 patients in this study who underwent post-alectinib/pre-brigatinib biopsies, 5 had an ALK I1171X or V1180L resistance mutation; of these, 1 had a confirmed partial response and 3 had stable disease on brigatinib. One patient had an ALK G1202R mutation in a post-alectinib/pre-brigatinib biopsy, and had progressive disease as the best overall response to brigatinib. Conclusions: Brigatinib has limited clinical activity in alectinib-refractory ALK-positive NSCLC. Additional studies are needed to establish biomarkers of response to brigatinib and to identify effective therapeutic options for alectinib-resistant ALK-positive NSCLC patients. (C) 2018 International Association for the Study of Lung Cancer. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1530 / 1538
页数:9
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