Prostate Tissue Composition and MR MeasurementsWord文件下载.docx
《Prostate Tissue Composition and MR MeasurementsWord文件下载.docx》由会员分享,可在线阅读,更多相关《Prostate Tissue Composition and MR MeasurementsWord文件下载.docx(40页珍藏版)》请在冰豆网上搜索。
4.AnnaPlotkin,MD,
5.JohnTrachtenberg,MD,CM,
6.BrianC.Wilson,PhDand
7.MasoomA.Haider,MD
+AuthorAffiliations
1.1FromtheDepartmentofMedicalImaging,PrincessMargaretHospital,UniversityHealthNetworkandMountSinaiHospital,610UniversityAve,Room3-958,Toronto,ON,CanadaM5G2M9(D.L.L.,J.T.,M.A.H.);
InstituteofMedicalScience,UniversityofToronto,Toronto,Ontario,Canada(D.L.L.,M.A.H.);
DepartmentofPathologyandLaboratoryMedicine,TorontoGeneralHospital,UniversityHealthNetwork,Toronto,Ontario,Canada(T.H.v.d.K.,A.J.E.);
DepartmentofLaboratoryMedicineandPathobiology,UniversityofToronto,BantingInstitute,Toronto,Ontario,Canada(A.P.);
DepartmentofSurgicalOncology,PrincessMargaretHospital,UniversityHealthNetwork,UniversityofToronto,Toronto,Ontario,Canada(J.T.);
andDepartmentofMedicalBiophysics,UniversityofToronto,OntarioCancerInstitute,Toronto,Ontario,Canada(B.C.W.).
1.Addresscorrespondenceto
M.A.H.(e-mail:
m.haider@utoronto.ca).
1.Authorcontributions:
Guarantorsofintegrityofentirestudy,J.T.,M.A.H.;
studyconcepts/studydesignordataacquisitionordataanalysis/interpretation,allauthors;
manuscriptdraftingormanuscriptrevisionforimportantintellectualcontent,allauthors;
manuscriptfinalversionapproval,allauthors;
literatureresearch,D.L.L.,T.H.v.d.K.,A.J.E.,A.P.,J.T.;
clinicalstudies,T.H.v.d.K.,A.P.,J.T.;
experimentalstudies,D.L.L.,A.J.E.,A.P.,J.T.;
statisticalanalysis,D.L.L.;
andmanuscriptediting,allauthors
NextSection
Abstract
Purpose:
Toinvestigaterelationshipsbetweenmagneticresonance(MR)imagingmeasurementsandtheunderlyingcompositionofnormalandmalignantprostatetissue.
MaterialsandMethods:
Twenty-fourpatients(medianage,63years;
agerange,44–72years)gaveinformedconsenttobeexaminedforthisresearchethicsboard–approvedstudy.Beforeundergoingprostatectomy,patientswereexaminedwithT2-weighted,diffusion-weighted,T2mapping,anddynamiccontrastmaterial–enhancedMRimagingat1.5T.Mapsofapparentdiffusioncoefficient(ADC),T2,volumetransferconstant(Ktrans),andextravascularextracellularspace(ve)werecalculated.Whole-mounthematoxylin-eosin–stainedsectionsweregeneratedanddigitizedathistologicresolution.Percentageareasoftissuecomponents(nuclei,cytoplasm,stroma,luminalspace)weremeasuredbyusingimagesegmentation.CorrespondingregionsonMRimagesandhistologicspecimensweredefinedbyusinganatomicallydefinedsegmentsinperipheralzone(PZ)andcentralglandtissue.CancerandnormalPZregionswereidentifiedathistopathologicanalysis.EachMRparameter–histologictissuecomponentpairwasassessedbyusinglinearmixed-effectsmodels,andcancerversusnormalPZvalueswerecomparedbyusingnonparametrictests.
Results:
ADCandT2wereinverselyrelatedtopercentageareaofnucleiandpercentageareaofcytoplasmandpositivelyrelatedtopercentageareaofluminalspace(P≤.01).ThesetrendswerereversedforKtrans(P<
.001).Ktranshadasignificantlynegative(P=.01)slopeversuspercentageareaofstroma,andvehadapositive(P=.008)slopeversuspercentageareaofstroma.Thevewasinverselyproportionaltothepercentageareaofnuclei(P=.05).AllMRimagingparameters(P≤.05)andthepercentageareasofalltissuecomponents(P≤.001)exceptstroma(P>
.48)weresignificantlydifferentbetweencancerandnormalPZtissue.
Conclusion:
MRimaging–derivedparametersmeasuredintheprostateweresignificantlyrelatedtotheproportionofspecifichistologiccomponentsthatdifferbetweennormalandmalignantPZtissue.Theserelationshipsmayhelpdefineimaging-relatedhistologicprognosticparametersforprostatecancer.
PreviousSectionNextSection
Introduction
Inprostatecancer,clinicalfactorssuchasGleasonscoreatbiopsy,prostate-specificantigenlevel,andtumorstageareassessedbeforetreatmenttoestimatelong-termpatientoutcome
(1)andinfluencethechoiceoftherapy.MorphologicfeaturessuchasnucleusorlumensizehavebeenshownquantitativelytoberelatedtoprimaryGleasonscorepattern
(2)anddiseaseprogression(3)andhavethepotentialtocontributetotreatmentmanagementstrategies.However,duetosamplingerror,thepropertiesoftissuecollectedfrombiopsymaynotaccuratelyreflectthetissuepropertiesdeterminedafterradicalprostatectomy(4).Volumetricassessmentofprostatecancerwithmagneticresonance(MR)imagingmayassistinlocalizingthetumor(5–8),identifyingclinicallynonimportantcancers(9),and/orpredictingbiochemicaltreatmentfailure(10).Inaddition,diffusion-weightedimaginganddynamiccontrastmaterial–enhancedMRimagingfacilitateadditionalcharacterizationofprostatecancer,withquantitativedifferencesbetweennormalandmalignantperipheralzone(PZ)tissuereported(11–20).RecentworkhasalsorevealedacorrelationbetweenMRimagingfindingsandimmunohistochemicalmarkersofproliferation(21,22).Thus,furtherelucidationoftherelationshipsbetweenMRimagingfindingsandcorrespondinghistologicfeaturescouldhaveatremendouseffectonpatientcare,facilitatingguidedbiopsyatthemostaggressivelocationofprostatecancerand/orrevealingsurrogatesforpropertiesrelatedtooutcome.
HistopathologiccorrelatestoT2-weightedsignalintensityintheprostatehavebeeninvestigated(23,24),andmorerecently,aninverserelationshipbetweenapparentdiffusioncoefficient(ADC)andcellulardensityhasbeendetermined(22,25).ThestudyofpropertiesbeyondcellulardensityandnucleusareameasurementsandtherangeofMRimagingparametersinvestigatedhavebeenlimited.Inaddition,histopathologicanalysisofselectedregionsintheavailabletissuehaspotentiallyintroducedbias.Inthecurrentwork,weinvestigatedtherelationshipsbetweenvarioustissuecomponents(percentagesofnuclei,epithelialcytoplasm,stroma,andluminalspace)andinvivoMRimagingparameters(ADC,T2,volumetransferconstant[Ktrans],extravascularextracellularvolumefraction[ve])byusingwhole-mounthistologicsectionsdigitizedintheirentirety,objectivemethodsofregisteringPZandcentralgland(CG)tissueathistologicanalysisandimaging,andhistopathologicallydefinedPZtumors.ThepurposeofthisstudywastoinvestigatetherelationshipsbetweenMRimagingmeasurementsandtheunderlyingcompositionofnormalandmalignantprostatetissue.
MaterialsandMethods
Patients
TheinstitutionalresearchethicsboardoftheUniversityHealthNetworkapprovedthisstudy,andallpatientsgaveinformedconsent.Thirty-oneconsecutivepatientswereenrolledbetweenJune1,2006,andFebruary15,2008,aspartofanongoingprospectivestudy,andalldatawereretrospectivelyreviewed.Theparticipatingpatientshadundergonenopriortreatmentforprostatecancer,hadnocontraindicationstoMRimagingorcontrastagentadministration,andhadnoevidenceofnodalorbonemetastases,asdeterminedwithpreoperativeimaging.Sevenpatientswereexcludedfromanalysisbecausetheirhistologicslideswereunavailableforreview(n=2)orcouldnotbedigitized(n=5).Onepatientwasexcludedfromdynamiccontrast-enhancedMRimaginganalysisowingtosubstantialmotionduringimageacquisition.Theclinicaldataforthe24patientsexaminedinthisstudyaresummarizedinTable1.
Viewthistable:
Inthiswindow
Inanewwindow
Table1
Characteristicsof24PatientswithProstateCancer
MRImagingProtocol
Beforeundergoingsurgery,allpatientswereexaminedwithMRimaging,whichwasperformedwitha1.5-Tsystem(ExciteHD;
GEHealthcare,Milwaukee,Wis)byusingafour-channelphased-arraysurfacecoilcoupledtoanendorectalcoil(Medrad,Warrendale,Pa).Inthelatterpatientcohortof11patients,theendorectalcoilwasfilledwitha100%wt/volbariumsulfatesuspension(LiquidPolibar;
E-Z-Em,Westbury,NY)(26)toreducemagneticsusceptibilityartifacts.ThemediantimebetweenbiopsyandMRimagingwas70days(range,31–266days),andthatbetweenMRimagingandsurgerywas13days(range,1–139days).Axial-obliquefastspin-echoT2-weighted,echo-planardiffusion-weighted(bvalues,0and600sec/mm2),multiechofastspin-echoforT2-mapping,anddynamiccontrast-enhancedMRimageswereobtainedwiththeimagingplaneperpendiculartotherectalwall–prostateinterface.Dynamiccontrast-enhancedMRimagingdataconsistedoftwodatasets:
dataobtainedwithmultisectionmultiple-flip-anglefastspoiledgradient-recalledacquisitioninthesteadystateforT1mappinganddatasubsequentlyobtainedduring50phasesofmultisectionfastspoiledgradient-recalledacquisitioninthesteadystate(26sections,temporalresolutionof10seconds).Twobaselineimageswereacquiredbeforetheinjectionof20mLofgadopentetatedimeglumine(Magnevist;
BayerScheringPharma,Berlin,Germany)andthena20-mLsalineflush,whichwereadministeredatarateof4mL/secbyusingapowerinjector(SpectrisMRInjectionSystem;
Medrad).
T2-weighted,diffusion-weighted,andmultiechofastspin-echoMRimageswereacquiredwithleft-to-rightphaseencoding.Anterior-posteriorphaseencodingwasperformedforalldynamiccontrast-enhancedMRimagingexaminations.Thesectionlocation,sectionthickness(3mm),andintersectiongap(0mm)werekeptconsistent.AllotherMRimageacquisitionparametersar