A Phase II Randomized Study of Cisplatin-Pemetrexed plus either Enzastaurin or Placebo in Chemonaive Patients with Advanced Non-Small Cell Lung Cancer

被引:13
作者
Vansteenkiste, Johan [1 ]
Ramlau, Rodryg [2 ]
von Pawel, Joachim [4 ]
San Antonio, Belen [7 ]
Eschbach, Corinna [5 ]
Szczesna, Aleksandra [3 ]
Kennedy, Liam [8 ]
Visseren-Grul, Carla [9 ]
Chouaki, Nadia [10 ]
Reck, Martin [6 ]
机构
[1] Univ Hosp Gasthuisberg, Resp Oncol Unit Pulmonol, BE-3000 Louvain, Belgium
[2] Karol Marcinkowski Univ Med Sci, Ctr Pneumol & Thorac Surg, Poznan, Poland
[3] Reg Lung Dis Hosp, Otwock, Poland
[4] Asklepios Hosp Munich Gauting, Munich, Germany
[5] Asklepios Hosp Hamburg, Hamburg, Germany
[6] Hosp Grosshansdorf, Grosshansdorf, Germany
[7] Eli Lilly & Co, Madrid, Spain
[8] Eli Lilly & Co, Surrey, England
[9] Eli Lilly & Co, Houten, Netherlands
[10] Eli Lilly & Co, Paris, France
关键词
Enzastaurin; Non-small cell lung cancer; Cisplatin-pemetrexed; C-BETA-INHIBITOR; COMBINATION; GEMCITABINE;
D O I
10.1159/000335268
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Enzastaurin is a serine/threonine kinase inhibitor that targets protein kinase C and AKT pathways. Enzastaurin and pemetrexed demonstrated synergy in preclinical studies. This trial was designed to evaluate the safety and efficacy of first-line enzastaurin plus cisplatin-pemetrexed in advanced non-small cell lung cancer (NSCLC). Methods: A safety lead-in phase (n = 13) of enzastaurin 125 or 250 mg twice daily was added to cisplatin-pemetrexed. A subsequent randomized, placebo-controlled phase II study (n = 22) of the combination was conducted to evaluate efficacy. Results:The combination was well tolerated and showed activity, with 7 (53.8%, 95% Cl 26.7-80.9) confirmed partial responses and 2 stable diseases in 13 treated patients in the lead-in phase. However, the study was terminated early based on interim results from two phase II NSCLC studies of enzastaurin plus cytotoxic chemotherapy, which indicated no efficacy improvement. Conclusions: Enzastaurin and cisplatin-pemetrexed is tolerable with preliminary activity in patients with advanced NSCLC, but because of a lack of efficacy improvement in other phase II NSCLC studies, the study was terminated early. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:25 / 29
页数:5
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