叶黄素
刺猬
腺癌
医学
刺猬信号通路
内科学
肿瘤科
化学
奥沙利铂
癌症
信号转导
生物化学
结直肠癌
作者
Andrew H. Ko,Noelle K. LoConte,Margaret A. Tempero,Evan J. Walker,Robin Kate Kelley,Stephanie Lewis,Wei‐Chou Chang,Emily Kantoff,Michael W. Vannier,Daniel V.T. Catenacci,Alan P. Venook,Hedy L. Kindler
出处
期刊:Pancreas
[Lippincott Williams & Wilkins]
日期:2015-09-19
卷期号:45 (3): 370-375
被引量:205
标识
DOI:10.1097/mpa.0000000000000458
摘要
Objectives In mouse models of pancreatic cancer, IPI-926, an oral Hedgehog inhibitor, increases chemotherapy delivery by depleting tumor-associated stroma. This multicenter phase Ib study evaluated IPI-926 in combination with FOLFIRINOX (5-fluorouracil, leucovorin, irinotecan, oxaliplatin) in patients with advanced pancreatic cancer. Methods Patients were treated with once-daily IPI-926 plus FOLFIRINOX. A 3 + 3 dose escalation design was used, with cohort expansion at the maximum tolerated dose. A subset of patients underwent perfusion computed tomography to assess changes in tumor perfusion. Results The maximum tolerated dose was identified 1 dose level below standard FOLFIRINOX. Common treatment-related adverse events included liver function test abnormalities, neuropathy, nausea/vomiting, and diarrhea. Objective response rate was high (67%), and patients receiving IPI-926 maintenance showed further declines in CA19-9 levels even after FOLFIRINOX discontinuation. Treatment did not result in consistent increases in tumor perfusion. The study closed early when a separate phase II trial of IPI-926 plus gemcitabine indicated detrimental effects of this combination. Conclusions This is the first study to demonstrate the feasibility of using FOLFIRINOX as the chemotherapeutic backbone in a clinical trial design. Although robust antitumor activity and acceptable safety were observed with the addition of IPI-926 to this regimen, future development of Hedgehog inhibitors in pancreatic cancer seems unlikely.
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