Evaluation of BAY43-9006/Cetuximab in Colorectal Cancer
Evaluation of BAY43-9006/Cetuximab in Colorectal Cancer
批准号:
7513154
负责人:
Wells A. Messersmith
金额:
$24.63万
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-12-24 至 2011-05-31
关键词:
Antineoplastic AgentsApoptosisBAY 43-9006Bevacizumab/CetuximabBindingBiologicalBiological MarkersBiopsyCYP3A4 geneCancer EtiologyCancer PatientCell LineCessation of lifeCetuximabCetuximab/IrinotecanClinicClinicalClinical TrialsColon CarcinomaColorectal CancerCytotoxic agentDataDevelopmentDigit structureDiseaseDrug KineticsEpidermal Growth Factor ReceptorEvaluationFine needle aspiration biopsyFluorouracilFoundationsGenesGoalsIrinotecan/OxaliplatinLaboratoriesLifeMeasuresMidazolamMolecular TargetMutationNormal tissue morphologyOncogenicOralPDGFRB genePathway interactionsPatientsPharmaceutical PreparationsPharmacodynamicsPhasePhase II/III TrialPhase III Clinical TrialsPopulationPrincipal InvestigatorProliferative IndexRaf Kinase InhibitorRas/RafRateReceptor SignalingRenal Cell CarcinomaResearch PersonnelResistanceSN-38SN-38GSamplingScheduleSignal PathwaySignal TransductionSignal Transduction InhibitorSolid NeoplasmStandards of Weights and MeasuresTechnologyTestingTherapeuticTissue SampleToxic effectTumor TissueVascular Endothelial Growth Factor ReceptorVascular Endothelial Growth FactorsWeekWorkXenograft procedureangiogenesisantibody inhibitorbasebevacizumabcell growthclinical efficacycombinatorialdaydesignfluorodeoxyglucose positron emission tomographyimprovedindexinginhibitor/antagonistirinotecanneoplastic cellnovelprogramsresponsetumor
中文摘要
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英文摘要
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.
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依托单位:
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财政年份:2008
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依托单位:
BAY 43-9006 IN COMBINATION WITH CETUXIMAB AND IRINOTECAN
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批准号:7604649
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项目类别:
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Evaluation of Oral EGFR Inhibitors in Colorectal Cancer
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批准号:7501958
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项目类别:
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资助金额:$13.77万
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财政年份:2005
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依托单位:
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