A phase 1b study of crenigacestat (LY3039478) in combination with gemcitabine and cisplatin or gemcitabine and carboplatin in patients with advanced or metastatic solid tumors

被引:8
|
作者
Massard, C. [1 ]
Cassier, P. A. [2 ]
Azaro, A. [3 ,4 ]
Anderson, B. [5 ]
Yuen, E. [5 ]
Yu, D. [5 ]
Oakley, G., III [5 ]
Benhadji, K. A. [6 ]
Pant, S. [7 ]
机构
[1] Univ Paris Sud, Univ Paris Saclay, Drug Dev Dept DITEP, Inserm Unit U981,Gustave Roussy, Villejuif, France
[2] Ctr Leon Berard, Dept Med Oncol, Lyon, France
[3] Vall dHebron Univ Hosp, Dept Med Oncol, Mol Therapeut Res Unit, Barcelona, Spain
[4] Univ Autonoma Barcelona UAB, Dept Pharmacol, Barcelona, Spain
[5] Eli Lilly & Co, Indianapolis, IN 46285 USA
[6] Eli Lilly & Co, New York, NY USA
[7] Univ Texas Med Ctr MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Div Canc Med, Houston, TX USA
关键词
LY3039478; Crenigacestat; Notch inhibition; Metastatic cancer; POPULATION PHARMACOKINETICS; SIGNALING PATHWAY; CANCER PATIENTS; NOTCH; RESISTANCE; CELLS; INHIBITION; ACTIVATION;
D O I
10.1007/s00280-022-04461-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Notch signaling plays an integral role in development and tissue homeostasis. Inhibition of Notch signaling has been identified as a reasonable target for oncotherapy. Crenigacestat (LY3039478) is a potent Notch inhibitor that decreases Notch signaling and its downstream biologic effects. Methods I6F-MC-JJCD was a multicenter, nonrandomized, open-label, phase 1b study with 5 separate, parallel dose escalations in patients with advanced or metastatic cancer from a variety of solid tumors followed by a dose-confirmation phase in pre-specified tumor types. This manuscript reports on 2 of 5 groups. The primary objective was to determine the recommended phase 2 dose of crenigacestat combined with other anticancer agents (gemcitabine/cisplatin or gemcitabine/carboplatin). Secondary objectives included evaluation of safety, tolerability, preliminary efficacy, and pharmacokinetics. Results Patients (N = 31) received treatment between November 2016 and July 2019. Dose-limiting toxicities occurred in 6 patients. The recommended phase 2 dose for crenigacestat was 50 mg TIW in Part 1 (combined with gemcitabine/cisplatin) and not established in Part 2 (combined with gemcitabine/carboplatin) due to poor tolerability. Patients had at least one treatment-emergent adverse event (TEAE), and most had Grade >= 3 TEAEs. Over 50% of the patients experienced gastrointestinal disorders (Grade >= 3). No patient had complete response; 5 patients had a partial response. Disease control rates were 62.5% (Part 1) and 60.0% (Part 2). Conclusion This study demonstrated that the Notch inhibitor, crenigacestat, combined with different anticancer agents (gemcitabine, cisplatin, and carboplatin) was poorly tolerated and resulted in disappointing clinical activity in patients with advanced or metastatic solid tumors. Clinicaltrials.gov Identification Number: NCT02784795.
引用
收藏
页码:335 / 344
页数:10
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