国际慢性胃炎分期分级标准OLGA
631
STOMACHANDDUODENUM
Gastritisstaginginclinicalpractice:theOLGAstagingsystem
MassimoRugge,AlbertoMeggio,GianmariaPennelli,FrancescoPiscioli,LucianoGiacomelli,GiovanniDePretis,DavidYGraham
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Gut2007;56:631–636.doi:10.1136/gut.2006.106666
Seeendofarticleforauthors’affiliations
........................Correspondenceto:
MassimoRugge,AnatomiaPatologica,Universita`degliStudidiPadova,Istituto
OncologicodelVenetoIOV-IRCCS,ViaAristideGabelli,61,35121Padova,Italia;massimo.rugge@unipd.itRevised14September2006Accepted11October2006PublishedOnlineFirst1December2006
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Background:Theavailableclassificationsofgastritisareinconsistentlyused,possiblybecausenoneprovidesimmediateprognostic/therapeuticinformationtoclinicians.Ashistologyreportingofhepatitisintermsofstageisclinicallyusefulandwidelyaccepted,aninternationalgroup(OperativeLinkonGastritisAssessment(OLGA))proposedanequivalentstagingsystemforreportinggastrichistology.Gastritisstagingintegratestheatrophyscore(obtainedbybiopsy)andtheatrophytopography(achievedthroughdirectedbiopsymapping).
Aim:Totestinaprospectivecross-sectionalstudywhetherOLGAstagingconsistentlystratifiedpatientsaccordingtotheircancerriskandprovidedclearprognostic/therapeuticinformation.
Methods:OLGAstagingforgastriccancerrisk(0–IV)andgastritisgrading(overallscoreoftheinflammatoryinfiltrate,grade1–4)wereappliedin439prospectivelyenrolled,consecutive,dyspepticoutpatientswhounderwentendoscopywithstandardisedbiopsysampling.Incidentalneoplasticlesionsandcoexistingpepticulcerswererecorded.Resultswerepresentedasstage(includingantral(A)andcorpus(C)atrophyscores)andHpyloristatus(eg,A=3;C=2:stageIV;Hp+ve).
Results:Benignconditions(includingduodenalulcers;p,0.001)consistentlyclusteredinstages0–II,whereasallneoplastic(invasiveandnon-invasive)lesionsclusteredinstagesIII–IV(p,0.001).
Conclusions:Gastritisstaging,combinedwithHpyloristatus,providedclinicallyrelevantinformationontheoverallstatusofthegastricmucosawithimplicationsforprognosis,therapyandmanagement.
system.2223TheOLGAsystemusesthebiopsysamplingprotocolandthevisualanaloguescalesrecommendedbytheHouston-updatedSydneysystem.7IntheOLGAstagingsystem,gastricatrophyisconsideredtobethehistologicallesionrepresentativeofdiseaseprogression.Gastritisstageresultsfromcombiningtheextentofatrophyscoredhistologicallywiththetopographyofatrophyidentifiedthroughbiopsymapping.Ithasbeenalsosuggestedthatthediagnosticreportincludeinformationabouttheprobableaetiology.22
Thisprospectivecross-sectionalstudyaimedtovalidatetheOLGAgastritisstagingsystemasaroutinehistologyreportingsystem.Italsotestedwhetherthediagnosticmessageconveyedbythegastritisstageconsistentlyidentifiedpatientswithdifferentcancerriskandalsoprovidedclinicianswithclearprognosticandtherapeuticinformation.
astritisisaninflammatoryconditionofthegastricmucosa.1–6Thephenotypicspectrumofchronicgastricinflammationiswellestablished,andthebasicdistinc-tionbetweennon-atrophicandatrophicpatternsisbothinternationallyacceptedandconsistent.7–9Atrophyisdefinedas‘‘lossofappropriateglands’’andissubtypedintotwomainhistologicalvariants:atrophyresultingfromthedisappearanceofglandsandreplacementwithfibrosisofthelaminapropria;andglandularlossresultingfromreplacementofnativeglandswithmetaplastic,‘‘inappropriateforlocation’’glandularstruc-tures.17–9Long-termfollow-upstudiesconductedindifferentpopulationshaveconsistentlyconfirmedthattheextentofthemucosalatrophyparallelsgastriccancerrisk.10–17
TheSydneysystemanditsHouston-updatedversionattemptedtoimproveonWhitehead’sclassification18ofgastritisand,atthesametime,developareportingsystemtoassistthepathologist.346AlthoughtheSydneysystemiswidelycited,mostcitationsrefertoitsfour-pointgradingsystemofthehistologicallesionsandnottotherecommendedformatofbiopsyreporting.
Currently,noreportingscheme/terminologyforchronicgastritisisavailablethatisbotheasilyunderstoodbycliniciansandpatientsandalsoprovidesprognosticandtherapeuticinformationinunequivocalterms.Thissituationcontrastsmarkedlywiththatofchronichepatitis,wherethe‘‘traditional’’histologicalreportwithdescriptivelabelshasbeenreplacedbyawidelyadoptedstagingsystem.19–21Hepatitisstaginghasprovedusefulinsimplifyingmedicalcommunication,monitoringtheprogressionofthediseaseandtheeffectsoftreatment,and,atthesametime,expressingthecancerriskassociatedwiththeprogressiontocirrhosisevolution.
Thesuccessfulexperienceofhepatitisstagingpromptedaninternationalgroupofgastroenterologistsandpathologists(OperativeLinkonGastritisAssessment(OLGA))todevelopahistologicalstagingsystemforgastricinflammatorydiseasesthatwouldmeetthesameobjectivesasthehepatitisstaging
G
PATIENTSANDMETHODS
Patients
Atotalof439consecutivedyspepticoutpatientsreferredtothegastroenterologyunitoftheRoveretoRegionalHospitalbetweenApril2004andApril2005wereprospectivelyenrolledinthestudy.Tominimisethevariabilityintheendoscopyprocedure(macroscopicassessmentandbiopsysamplingprotocol),onlypatientshavingconsecutiveuppergastrointest-inalendoscopyproceduresperformedbyonlyonetrainedgastroenterologist(AM),withspecificexpertiseinuppergastrointestinalendoscopy,wereenteredintothestudy.Patientclinicalhistorywasobtainedbytheendoscopistwhoperformedtheprocedure,whoalsoobtainedconsentfromthepatienttobeinvolvedinthestudy.
Exclusioncriteriawere(a)anyprevioussurgicalinterventiontotheuppergastrointestinaltractbecauseofeitheroesophagealorgastricdisease,(b)incompletegastricendoscopyprocedure
Abbreviations:OLGA,OperativeLinkonGastritisAssessment;PPI,protonpumpinhibitor
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