Evaluation of BAY43-9006/Cetuximab in Colorectal Cancer

BAY43-9006/西妥昔单抗在结直肠癌中的评价

基本信息

批准号：
7513154
负责人：
Wells A. Messersmith
金额：
$ 24.63万
依托单位：
UNIVERSITY OF COLORADO DENVER
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-12-24 至 2011-05-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7513154
关键词：
Antineoplastic Agents Apoptosis BAY 43-9006 Bevacizumab/Cetuximab Binding Biological Biological Markers Biopsy CYP3A4 gene Cancer Etiology Cancer Patient Cell Line Cessation of life Cetuximab Cetuximab/Irinotecan Clinic Clinical Clinical Trials Colon Carcinoma Colorectal Cancer Cytotoxic agent Data Development Digit structure Disease Drug Kinetics Epidermal Growth Factor Receptor Evaluation Fine needle aspiration biopsy Fluorouracil Foundations Genes Goals Irinotecan/Oxaliplatin Laboratories Life Measures Midazolam Molecular Target Mutation Normal tissue morphology Oncogenic Oral PDGFRB gene Pathway interactions Patients Pharmaceutical Preparations Pharmacodynamics Phase Phase II/III Trial Phase III Clinical Trials Population Principal Investigator Proliferative Index Raf Kinase Inhibitor Ras/Raf Rate Receptor Signaling Renal Cell Carcinoma Research Personnel Resistance SN-38 SN-38G Sampling Schedule Signal Pathway Signal Transduction Signal Transduction Inhibitor Solid Neoplasm Standards of Weights and Measures Technology Testing Therapeutic Tissue Sample Toxic effect Tumor Tissue Vascular Endothelial Growth Factor Receptor Vascular Endothelial Growth Factors Week Work Xenograft procedure angiogenesis antibody inhibitor base bevacizumab cell growth clinical efficacy combinatorial day design fluorodeoxyglucose positron emission tomography improved indexing inhibitor/antagonist irinotecan neoplastic cell novel programs response tumor

项目摘要

DESCRIPTION (provided by applicant): Colorectal cancer will claim approximately 55,000 lives in the U.S. in 2005, and although recent advances have been improved survival incrementally, new treatment options and strategies are desperately needed. Cell signaling inhibitors have recently emerged as a successful anti-tumor strategy, and an antibody inhibitor of the EGFR pathway has made it to the colon cancer clinic. Another attractive target for anticancer drugs is the Ras/Raf/Mek/Erk signaling cascade, which promotes tumor cell growth, angiogenesis, and resistance to apoptosis. Mutations that constitutively activate the Ras oncogenic signaling pathway are highly prevalent in colorectal cancer (50-70%). In addition, the Ras pathway is part of the signaling network for EGFR, which is a validated target in colorectal cancer. One major obstacle to the development of signal transduction inhibitors is cross-talk between signaling pathways, which can subvert the effects of a given inhibitor. Our laboratory has found that combinations of inhibitors may overcome this challenge, where a cell line xenograft that is resistant to an EGFR or Erk inhibitor alone becomes sensitive when the two are combined. BAY 43-9006 is a novel oral Raf kinase inhibitor with inhibitory activity against VEGFR and PDGFR as well. We hypothesize that combining BAY 43-9006 with the standard treatment for chemoresistant advanced colorectal cancer (irinotecan/cetuximab) will result in synergistic antitumor effects. The goal is to complete a phase I/I I clinical, pharmacological, and biological study of BAY 43-9006 in combination with cetuximab and irinotecan in patients with advanced colorectal cancer. Utilizing a lead-in design of BAY 43-9006 with cetuximab, combined with pre- and post treatment tumor and normal tissue samples, the biological effects of this combination will be fully characterized. Phamacokinetic and pharmacodynamic studies of this combination will represent the foundation and rationale for further studies.

描述（由申请人提供）： 2005 年，结直肠癌将在美国夺去大约 55,000 人的生命，尽管最近的进展已逐渐提高了生存率，但仍迫切需要新的治疗选择和策略。细胞信号抑制剂最近已成为一种成功的抗肿瘤策略，EGFR 通路的抗体抑制剂已进入结肠癌临床。抗癌药物的另一个有吸引力的靶点是 Ras/Raf/Mek/Erk 信号级联，它促进肿瘤细胞生长、血管生成和抗凋亡。组成性激活 Ras 致癌信号通路的突变在结直肠癌中非常普遍 (50-70%)。此外，Ras 通路是 EGFR 信号网络的一部分，而 EGFR 是结直肠癌中经过验证的靶点。信号转导抑制剂开发的一个主要障碍是信号通路之间的串扰，这可能会破坏给定抑制剂的作用。我们的实验室发现，抑制剂的组合可以克服这一挑战，其中对 EGFR 或 Erk 抑制剂单独具有抗性的细胞系异种移植物在两者组合时变得敏感。 BAY 43-9006 是一种新型口服 Raf 激酶抑制剂，对 VEGFR 和 PDGFR 也具有抑制活性。我们假设将 BAY 43-9006 与化疗耐药的晚期结直肠癌标准治疗（伊立替康/西妥昔单抗）相结合将产生协同抗肿瘤作用。目标是完成 BAY 43-9006 联合西妥昔单抗和伊立替康治疗晚期结直肠癌患者的 I/II I 期临床、药理学和生物学研究。利用BAY 43-9006与西妥昔单抗的导入设计，结合治疗前后的肿瘤和正常组织样本，将充分表征该组合的生物学效应。该组合的药代动力学和药效学研究将为进一步研究奠定基础和基本原理。