imvigor 210 cohort first-line atezolizumab cisplatin ineligible metastatic urothelial队列一线Atezolizumab中顺铂符号转移性尿路上皮癌.pptx
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CCOIndependentConferenceCoverage*
ofthe2016ASCOAnnualMeeting,June3-7,2016IMvigor210(Cohort1):First-lineAtezolizumabinCisplatin-IneligibleMetastaticUrothelialCarcinoma*CCOisanindependentmedicaleducationcompanythatprovidesstate-of-the-artmedicalinformationtohealthcareprofessionalsthroughconferencecoverageandothereducationalprograms.ThisactivityissupportedbyeducationalgrantsfromAmgen,Ariad,
BayerHealthcarePharmaceuticals,CelgeneCorporation,Genentech,Incyte,Merck,andTaihoPharmaceuticals.
IMvigor210(Cohort1):BackgroundCisplatintheisfirst-linestandardofcareformetastaticurothelialcarcinomaMostptsarecisplatinineligibleduetopoorperformancestatus,impairedrenalfunction,orcomorbidities[1]Non-cisplatin–basedregimensassociatedwithshortresponseduration,lackofsurvivalbenefit,highdiscontinuationrate[2]Atezolizumab:engineeredmAbtargetingPD-L1immunecheckpointActive,welltoleratedintreatment-experiencedmUC[3]CurrentlyFDAapprovedonlyincisplatin-treatedptsCohort1oftheIMvigor210studyevaluatedsafety,efficacyofatezolizumabasfirst-linetherapyinuntreated,cisplatin-ineligiblemUCpts[4]1.GalaskyMD.ECC2015.Abstract2624.2.DeSantisM,etal.JClinOncol.2012;30:191-199.3.RosenbergJE,etal.Lancet.2016;387:1909-1920.
4.BalarAV,etal.ASCO2016.AbstractLBA4500.Slidecredit:
Single-armphaseIIstudywith2cohorts[1]IMvigor210:StudyDesignPtswithinoperableadvancedormetastaticUC,predominantlyTCChistology,evaluabletumortissuefor
PD-L1testing(N=429)Cohort1:(n=119)[2]previouslyuntreated,cisplatinineligible*Cohort2:(n=310)[3]priorplatinumtreatmentSlidecredit:Atezolizumab1200mgIVQ3WuntilPDAtezolizumab1200mgIVQ3Wuntillossofbenefit1.ClinicalTrials.gov.NC2.BalarAV,etal.ASCO2016.AbstractLBA4500.3.DreicerR,etal.ASCO2016.Abstract4515.Cohort1studyPrimaryendpoint:confirmedORRb
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