ASCEND-7: Efficacy and Safety of Ceritinib Treatment in Patients with ALK-Positive Non-Small Cell Lung Cancer Metastatic to the Brain and/or Leptomeninges

被引:34
作者
Chow, Laura Q. M. [1 ,2 ]
Barlesi, Fabrice [3 ]
Bertino, Erin M. [4 ,5 ]
van den Bent, Martin J. [6 ]
Wakelee, Heather A. [7 ]
Wen, Patrick Y. [8 ]
Chiu, Chao-Hua [9 ]
Orlov, Sergey [10 ]
Chiari, Rita [11 ]
Majem, Margarita [12 ]
McKeage, Mark [13 ]
Yu, Chong-Jen [14 ]
Garrido, Pilar [15 ]
Hurtado, Felipe K. [16 ]
Arratia, Pilar Cazorla [16 ]
Song, Yuanbo [16 ]
Branle, Fabrice [17 ]
Shi, Michael [16 ]
Kim, Dong-Wan [18 ,19 ]
机构
[1] Univ Washington, Seattle, WA 98195 USA
[2] Univ Texas Austin, Med Sch, Dept Oncol, Austin, TX 78712 USA
[3] Aix Marseille Univ, AP HM, CRCM, CNRS,INSERM, Marseille, France
[4] Ohio State Univ, Comprehens Canc Ctr, Arthur G James Canc Hosp, Columbus, OH 43210 USA
[5] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43210 USA
[6] Univ Med Ctr Rotterdam, Erasmus MC Canc Inst, Dept Neurol, Rotterdam, Netherlands
[7] Stanford Univ, Stanford, CA 94305 USA
[8] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[9] Natl Yang Ming Univ, Taipei Vet Gen Hosp, Dept Chest Med, Taipei, Taiwan
[10] State Pavlov Med Univ, St Petersburg, Russia
[11] AULSS6 Euganea, Dept Oncol, Padua, Italy
[12] Hosp Santa Creu & Sant Pau, Barcelona, Spain
[13] Univ Auckland, Auckland, New Zealand
[14] Natl Taiwan Univ Hosp, Dept Internal Med, Taipei, Taiwan
[15] Hosp Univ Ramon Y Cajal, Dept Med Oncol, Madrid, Spain
[16] Novartis Pharmaceut, E Hanover, NJ USA
[17] Novartis Pharma AG, Basel, Switzerland
[18] Seoul Natl Univ, Dept Internal Med, Coll Med, Seoul, South Korea
[19] Seoul Natl Univ Hosp, Seoul, South Korea
关键词
TYROSINE KINASE INHIBITORS; OPEN-LABEL; CRIZOTINIB; CHEMOTHERAPY; SURVIVAL; MANAGEMENT; DIAGNOSIS; CARCINOMATOSIS; ALECTINIB; OUTCOMES;
D O I
10.1158/1078-0432.CCR-21-1838
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Central nervous system metastases are a prominent cause of morbidity and mortality in patients with ALK-positive (ALK(+)) non-small cell lung cancer (NSCLC). The phase II ASCEND-7 (NCT02336451) study was specifically designed to assess the efficacy and safety of the ALK inhibitor (ALKi) ceritinib in patients with ALK(+) NSCLC metastatic to the brain and/or leptomeninges. Patients and Methods: Patients with active brain metastases were allocated to study arms 1 to 4 based on prior exposure to an ALKi and/or prior brain radiation (arm 1: prior radiotherapy/ALKi-pretreated; arm 2: no radiotherapy/ALKi-pretreated; arm 3: prior radiotherapy/ALKi-naive; arm 4: no radiotherapy/ALKi-naive). Arm 5 included patients with leptomeningeal carcinomatosis. Patients received ceritinib 750 mg once daily (fasted condition). Primary endpoint was investigator-assessed whole-body overall response rate (ORR) per RECIST v1.1. Secondary endpoints included disease control rate (DCR) and intracranial/extracranial responses. Results: Per investigator assessment, in arms 1 (n = 42), 2 (n = 40), 3 (n = 12), and 4 (n = 44), respectively: whole-body ORRs [95% confidence interval (CI)] were 35.7% (21.6-52.0), 30.0% (16.6-46.5), 50.0% (21.1-78.9), and 59.1% (43.2-73.7); whole-body DCR (95% CI): 66.7% (50.5-80.4), 82.5% (67.2-92.7), 66.7% (34.9-90.1), and 70.5% (54.8-83.2); intracranial ORRs 95%) CI): 39.3% (21.5-59.4), 27.6% (12.7-47.2), 28.6% (3.7-71.0), and 51.5% (33.5-69.2). In arm 5 (n = 18), whole-body ORR was 16.7% (95% CI, 3.6-41.4) and DCR was 66.7% (95% CI, 41.0-86.7). Paired cerebrospinal fluid and plasma sampling revealed that ceritinib penetrated the human blood-brain barrier. Conclusions: Ceritinib showed antitumor activity in patients with ALK+ NSCLC with active brain metastases and/or leptomeningeal disease, and could be considered in the management of intracranial disease.
引用
收藏
页码:2506 / 2516
页数:11
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