Lymphoma - Wikipedia

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Lymphoma is a group of blood and lymph tumors that develop from lymphocytes (a type of white blood cell). ... In current usage the name usually refers to just the ... Lymphoma FromWikipedia,thefreeencyclopedia Jumptonavigation Jumptosearch Hematologiccancerthataffectslymphocytes MedicalconditionLymphomaFollicularlymphomareplacingalymphnodeSpecialtyHematologyandoncologySymptomsEnlargedlymphnodes,fever,sweats,unintendedweightloss,itching,feelingtired[1][2]RiskfactorsEpstein–Barrvirus,autoimmunediseases,HIV/AIDS,tobaccosmoking[2][3]DiagnosticmethodLymphnodebiopsy[1][2]TreatmentChemotherapy,radiationtherapy,protontherapy,targetedtherapy,surgery[1][2]PrognosisAveragefiveyearsurvival85%(USA)[4]Frequency4.9million(2015)[5]Deaths204,700(2015)[6] Lymphomaisagroupofbloodandlymphtumorsthatdevelopfromlymphocytes(atypeofwhitebloodcell).[7]Incurrentusagethenameusuallyreferstojustthecancerousversionsratherthanallsuchtumours.[7]Signsandsymptomsmayincludeenlargedlymphnodes,fever,drenchingsweats,unintendedweightloss,itching,andconstantlyfeelingtired.[1][2]Theenlargedlymphnodesareusuallypainless.[1]Thesweatsaremostcommonatnight.[1][2] Manysubtypesoflymphomasareknown.[8]Thetwomaincategoriesoflymphomasarethenon-Hodgkinlymphoma(NHL)(90%ofcases)[9][10]andHodgkinlymphoma(HL)(10%).[9]TheWorldHealthOrganization(WHO)includestwoothercategoriesastypesoflymphoma–multiplemyelomaandimmunoproliferativediseases.[11]Lymphomasandleukemiasareapartofthebroadergroupoftumorsofthehematopoieticandlymphoidtissues.[12] RiskfactorsforHodgkinlymphomaincludeinfectionwithEpstein–Barrvirusandahistoryofthediseaseinthefamily.[1]Riskfactorsforcommontypesofnon-Hodgkinlymphomasincludeautoimmunediseases,HIV/AIDS,infectionwithhumanT-lymphotropicvirus,immunosuppressantmedications,andsomepesticides.[2][13]Eatinglargeamountsofredmeatandtobaccosmokingmayalsoincreasetherisk.[3][14][15]Diagnosis,ifenlargedlymphnodesarepresent,isusuallybylymphnodebiopsy.[1][2]Blood,urine,andbonemarrowtestingmayalsobeusefulinthediagnosis.[2]Medicalimagingmaythenbedonetodetermineifandwherethecancerhasspread.[1][2]Lymphomamostoftenspreadstothelungs,liver,andbrain.[1][2] Treatmentmayinvolveoneormoreofthefollowing:chemotherapy,radiationtherapy,protontherapy,targetedtherapy,andsurgery.[1][2]Insomenon-Hodgkinlymphomas,anincreasedamountofproteinproducedbythelymphomacellscausesthebloodtobecomesothickthatplasmapheresisisperformedtoremovetheprotein.[2]Watchfulwaitingmaybeappropriateforcertaintypes.[2]Theoutcomedependsonthesubtypewithsomebeingcurableandtreatmentprolongingsurvivalinmost.[9]Thefive-yearsurvivalrateintheUnitedStatesforallHodgkinlymphomasubtypesis85%,[4]whilethatfornon-Hodgkinlymphomasis69%.[16]Worldwide,lymphomasdevelopedin566,000peoplein2012andcaused305,000deaths.[11]Theymakeup3–4%ofallcancers,makingthemasagrouptheseventh-mostcommonform.[11][17]Inchildren,theyarethethird-mostcommoncancer.[18]Theyoccurmoreofteninthedevelopedworldthanthedevelopingworld.[11] Contents 1Signsandsymptoms 1.1Mouth 2Diagnosis 2.1Classification 2.1.1Hodgkinlymphoma 2.1.2Non-Hodgkinlymphomas 2.1.3Epstein–Barrvirus-associatedlymphoproliferativediseases 2.1.4WHOclassification 2.1.5Previousclassifications 2.2Staging 2.3Differentialdiagnosis 3Treatment 3.1Low-grade 3.2High-grade 3.2.1Hodgkinlymphoma 3.3Palliativecare 3.4Supportivetreatment 4Prognosis 5Epidemiology 6History 7Research 8Otheranimals 9References 10Externallinks Signsandsymptoms[edit] Thelymphnodeswherelymphomamostcommonlydevelops Lymphomaandlymphaticsystem Lymphomamaypresentwithcertainnonspecificsymptoms;ifthesymptomsarepersistent,anevaluationtodeterminetheircause,includingpossiblelymphoma,shouldbeundertaken. Lymphadenopathy[19][20]orswellingoflymphnodes,istheprimarypresentationinlymphoma.Itisgenerallypainless. Bsymptoms(systemicsymptoms)–canbeassociatedwithbothHodgkinlymphomaandnon-Hodgkinlymphoma.Theyconsistof: Fever[19][20] Nightsweats[19][20] Weightloss[19][20] Othersymptoms: Anemia,bleeding,increasedsusceptibilitytoinfections[21] Lossofappetiteoranorexia[20] Fatigue[19][20] Respiratorydistressordyspnea[20] Itching[19][20] Mouth[edit] Asymptomaticsoftswelling,whichmayormaynotbeulcerated,isprimarilyseenonthetonsils,buccalmucosa,palate,gums,salivaryglands,tongue,thefloorofthemouth,andretromolarregion.[citationneeded] Diagnosis[edit] Aninitialevaluationofasuspectedlymphomaistomakea"touchprep"whereinaglassslideislightlypressedagainstexcisedlymphoidtissue,andsubsequentlystained(usuallyH&Estain)forevaluationunderlightmicroscopy. Lymphomaisdefinitivelydiagnosedbyalymph-nodebiopsy,meaningapartialortotalexcisionofalymphnodeexaminedunderthemicroscope.[22]Thisexaminationrevealshistopathologicalfeaturesthatmayindicatelymphoma.Afterlymphomaisdiagnosed,avarietyoftestsmaybecarriedouttolookforspecificfeaturescharacteristicofdifferenttypesoflymphoma.Theseinclude: Immunophenotyping Flowcytometry Fluorescenceinsituhybridizationtesting Classification[edit] Lymphnodewithmantlecelllymphoma(low-powerview,H&E) AccordingtotheWorldHealthOrganization(WHO),lymphomaclassificationshouldreflectinwhichlymphocytepopulationtheneoplasmarises.[23]Thus,neoplasmsthatarisefromprecursorlymphoidcellsaredistinguishedfromthosethatarisefrommaturelymphoidcells.[23]Mostmaturelymphoidneoplasmscomprisethenon-Hodgkinlymphomas.[23]Historically,maturehistiocyticanddendriticcell(HDC)neoplasmshavebeenconsideredmaturelymphoidneoplasms,sincetheseofteninvolvelymphoidtissue.[23] Lymphomacanalsospreadtothecentralnervoussystem,oftenaroundthebraininthemeninges,knownaslymphomatousmeningitis(LM).[24] Hodgkinlymphoma[edit] Mainarticle:Hodgkinlymphoma Hodgkinlymphomaaccountsforabout15%oflymphomas.[25]Itdiffersfromotherformsoflymphomasinitsprognosisandseveralpathologicalcharacteristics.AdivisionintoHodgkinandnon-Hodgkinlymphomasisusedinseveraloftheolderclassificationsystems.AHodgkinlymphomaismarkedbythepresenceofatypeofcellcalledtheReed–Sternbergcell.[26][27] Non-Hodgkinlymphomas[edit] Non-Hodgkinlymphomas,whicharedefinedasbeingalllymphomasexceptHodgkinlymphoma,aremorecommonthanHodgkinlymphoma.Awidevarietyoflymphomasareinthisclass,andthecauses,thetypesofcellsinvolved,andtheprognosesvarybytype.Thenumberofcasesperyearofnon-Hodgkinlymphomaincreaseswithage.Itisfurtherdividedintoseveralsubtypes.[citationneeded] Epstein–Barrvirus-associatedlymphoproliferativediseases[edit] Epstein–Barrvirus-associatedlymphoproliferativediseasesareagroupofbenign,premalignant,andmalignantdiseasesoflymphoidcells,i.e.Bcells,Tcells,NKcells,andhistiocytic-dendriticcellsinwhichoneormoreofthesecelltypesisinfectedwiththeEpstein–Barrvirus(EBV).Thevirusmayberesponsibleforthedevelopmentand/orprogressionofthesediseases.InadditiontoEBV-positiveHodgkinlymphomas,theWorldHealthOrganization(2016)includesthefollowinglymphomas,whenassociatedwithEBVinfection,inthisgroupofdiseases:Burkittlymphoma;largeBcelllymphoma,nototherwisespecified;diffuselargeBcelllymphomaassociatedwithchronicinflammation;fibrin-associateddiffuselargeBcelllymphoma;primaryeffusionlymphoma;plasmablasticlymphoma;extranodalNK/Tcelllymphoma,nasaltype;peripheralTcelllymphoma,nototherwisespecified;angioimmunoblasticTcelllymphoma;follicularTcelllymphoma;andsystemicTcelllymphomaofchildhood.[28] WHOclassification[edit] TheWHOclassification,publishedin2001andupdatedin2008,[29][30]isbaseduponthefoundationslaidwithinthe"revisedEuropean–Americanlymphomaclassification"(REAL).Thissystemgroupslymphomasbycelltype(i.e.thenormalcelltypethatmostresemblesthetumor)anddefiningphenotypic,molecular,orcytogeneticcharacteristics.Thefivegroupsareshowninthetable.HodgkinlymphomaisconsideredseparatelywithintheWHOandprecedingclassifications,althoughitisrecognizedasbeingatumor,albeitmarkedlyabnormal,oflymphocytesofmatureBcelllineage.[citationneeded] Ofthemanyformsoflymphoma,somearecategorizedasindolent(e.g.smalllymphocyticlymphoma),compatiblewithalonglifeevenwithouttreatment,whereasotherformsareaggressive(e.g.Burkitt'slymphoma),causingrapiddeteriorationanddeath.However,mostoftheaggressivelymphomasrespondwelltotreatmentandarecurable.Theprognosis,therefore,dependsonthecorrectdiagnosisandclassificationofthedisease,whichisestablishedafterexaminationofabiopsybyapathologist(usuallyahematopathologist).[31] Lymphomasubtypes(WHO2008) MatureBcellneoplasms DNA-microarrayanalysisofBurkitt'slymphomaanddiffuselargeB-celllymphoma(DLBCL)showingdifferencesingeneexpressionpatterns.Colorsindicatelevelsofexpression;greenindicatesgenesthatareunderexpressedinlymphomacells(ascomparedtonormalcells),whereasredindicatesgenesthatareoverexpressedinlymphomacells. B-cellchroniclymphocyticleukemia/smallcelllymphoma 3to4%oflymphomasinadults Smallrestinglymphocytesmixedwithvariablenumbersoflargeactivatedcells,lymphnodesdiffuselyeffaced CD5,surfaceimmunoglobulin 5-yearsurvivalrate50%.[32] Occursinolderadults,usuallyinvolveslymphnodes,bonemarrowandspleen,mostpatientshaveperipheralbloodinvolvement,indolent B-cellprolymphocyticleukemia Lymphoplasmacyticlymphoma(suchasWaldenströmmacroglobulinemia) Splenicmarginalzonelymphoma Hairycellleukemia Plasmacellneoplasms: Plasmacellmyeloma(alsoknownasmultiplemyeloma) Plasmacytoma Monoclonalimmunoglobulindepositiondiseases Heavychaindiseases ExtranodalmarginalzoneBcelllymphoma,alsocalledMALTlymphoma About5%oflymphomasinadults Variablecellsizeanddifferentiation,40%showplasmacelldifferentiation,homingofBcellstoepitheliumcreateslymphoepitheliallesions. CD5,CD10,surfaceIg Frequentlyoccursoutsidelymphnodes,veryindolent,maybecuredbylocalexcision NodalmarginalzoneBcelllymphoma Follicularlymphoma About40%oflymphomasinadults Small"cleaved"[cleft]cells(centrocytes)mixedwithlargeactivatedcells(centroblasts),usuallynodular("follicular")growthpattern CD10,surfaceIg About72–77%[33] Occursinolderadults,usuallyinvolveslymphnodes,bonemarrowandspleen,associatedwitht(14;18)translocationoverexpressingBcl-2,indolent Primarycutaneousfolliclecenterlymphoma Mantlecelllymphoma About3to4%oflymphomasinadults Lymphocytesofsmalltointermediatesizegrowingindiffusepattern CD5 About50[34]to70%[34] Occursmainlyinadultmales,usuallyinvolveslymphnodes,bonemarrow,spleenandGItract,associatedwitht(11;14)translocationoverexpressingcyclinD1,moderatelyaggressive DiffuselargeBcelllymphoma,nototherwisespecified About40to50%oflymphomasinadults Variable,mostresembleBcellsoflargegerminalcenters,diffusegrowthpattern VariableexpressionofCD10andsurfaceIg Five-yearsurvivalrate60%[35] Occursinallages,butmostcommonlyinolderadults,mayoccuroutsidelymphnodes,aggressive DiffuselargeB-celllymphomaassociatedwithchronicinflammation Epstein–BarrviruspositivediffuselargeB-celllymphoma,nototherwisespecified Lymphomatoidgranulomatosis Primarymediastinal(thymic)largeB-celllymphoma IntravascularlargeB-celllymphoma ALK+largeB-celllymphoma Plasmablasticlymphoma Primaryeffusionlymphoma LargeB-celllymphomaarisinginHHV8-associatedmulticentricCastleman'sdisease Burkittlymphoma/leukemia <1%oflymphomasintheUnitedStates Roundlymphoidcellsofintermediatesizewithseveralnucleoli,starry-skyappearancebydiffusespreadwithinterspersedapoptosis CD10,surfaceIg Five-yearsurvivalrate50%[36] EndemicinAfrica,sporadicelsewhere,morecommoninimmunocompromisedandchildren,oftenvisceralinvolvement,highlyaggressive MatureTcellandnaturalkiller(NK)cellneoplasms T-cellprolymphocyticleukemia T-celllargegranularlymphocyteleukemia AggressiveNKcellleukemia AdultT-cellleukemia/lymphoma ExtranodalNK/T-celllymphoma,nasaltype Enteropathy-associatedT-celllymphoma HepatosplenicT-celllymphoma BlasticNKcelllymphoma Mycosisfungoides/Sézarysyndrome Mostcommoncutaneouslymphoidmalignancy Usuallysmalllymphoidcellswithconvolutednucleithatofteninfiltratetheepidermis,creatingPautriermicroabscesseses CD4 5-yearsurvival75%[37] Localizedormoregeneralizedskinsymptoms,generallyindolent,inamoreaggressivevariant,Sézary'sdisease,skinerythemaandperipheralbloodinvolvement PrimarycutaneousCD30-positiveTcelllymphoproliferativedisorders Primarycutaneousanaplasticlargecelllymphoma Lymphomatoidpapulosis PeripheralT-celllymphomanototherwisespecified MostcommonTcelllymphoma Variable,usuallyamixsmalltolargelymphoidcellswithirregularnuclearcontours CD3 Probablyconsistsofseveralraretumortypes,oftendisseminatedandgenerallyaggressive AngioimmunoblasticTcelllymphoma Anaplasticlargecelllymphoma:ALK-positiveandALK-negativetypes Breastplant-associatedanaplasticlargecelllymphoma Precursorlymphoidneoplasms B-lymphoblasticleukemia/lymphomanototherwisespecified B-lymphoblasticleukemia/lymphomawithrecurrentgeneticabnormalities T-lymphoblasticleukemia/lymphoma 15%ofchildhoodacutelymphoblasticleukemiaand90%oflymphoblasticlymphoma.[29]: 635  Lymphoblastswithirregularnuclearcontours,condensedchromatin,smallnucleoliandscantcytoplasmwithoutgranules TdT,CD2,CD7 Itoftenpresentsasamediastinalmassbecauseofinvolvementofthethymus.ItishighlyassociatedwithNOTCH1mutations,andismostcommoninadolescentmales. Hodgkinlymphoma ClassicalHodgkinlymphomas: NodularsclerosisformofHodgkinlymphoma MostcommontypeofHodgkinlymphoma Reed-Sternbergcellvariantsandinflammation,usuallybroadscleroticbandsthatconsistofcollagen CD15,CD30 Mostcommoninyoungadults,oftenarisesinthemediastinumorcervicallymphnodes MixedcellularityHodgkinlymphoma Second-mostcommonformofHodgkinlymphoma ManyclassicReed-Sternbergcellsandinflammation CD15,CD30 Mostcommoninmen,morelikelytobediagnosedatadvancedstagesthanthenodularsclerosisformEpstein–Barrvirusinvolvedin70%ofcases Lymphocyte-rich Lymphocytedepletedornotdepleted Nodularlymphocyte-predominantHodgkinlymphoma Immunodeficiency-associatedlymphoproliferativedisorders Associatedwithaprimaryimmunedisorder Associatedwiththehumanimmunodeficiencyvirus(HIV) Post-transplant Associatedwithmethotrexatetherapy Primarycentralnervoussystemlymphomaoccursmostofteninimmunocompromisedpatients,inparticularthosewithAIDS,butitcanoccurintheimmunocompetent,aswell.Ithasapoorprognosis,particularlyinthosewithAIDS.Treatmentcanconsistofcorticosteroids,radiotherapy,andchemotherapy,oftenwithmethotrexate. Previousclassifications[edit] Severalpreviousclassificationshavebeenused,includingRappaport1956,Lennert/Kiel1974,BNLI,Workingformulation(1982),andREAL(1994). TheWorkingFormulationof1982wasaclassificationofnon-Hodgkinlymphoma.ItexcludedtheHodgkinlymphomasanddividedtheremaininglymphomasintofourgrades(low,intermediate,high,andmiscellaneous)relatedtoprognosis,withsomefurthersubdivisionsbasedonthesizeandshapeofaffectedcells.Thispurelyhistologicalclassificationincludednoinformationaboutcellsurfacemarkers,orgenetics,anditmadenodistinctionbetweenT-celllymphomasandB-celllymphomas.Itwaswidelyacceptedatthetimeofitspublicationbutisnowobsolete.[38] In1994,theRevisedEuropean-AmericanLymphoma(REAL)classificationappliedimmunophenotypicandgeneticfeaturesinidentifyingdistinctclinicopathologicentitiesamongallthelymphomasexceptHodgkinlymphoma.[39]Forcodingpurposes,theICD-O(codes9590–9999)[40]andICD-10(codesC81-C96)[41]areavailable. Staging[edit] Diagramshowingcommonsiteswherelymphomaspreads Afteradiagnosisandbeforetreatment,cancerisstaged.Thisreferstodeterminingifthecancerhasspread,andifso,whetherlocallyortodistantsites.StagingisreportedasagradebetweenI(confined)andIV(spread).Thestageofalymphomahelpspredictapatient'sprognosisandisusedtohelpselecttheappropriatetherapy.[42] TheAnnArborstagingsystemisroutinelyusedforstagingofbothHLandNHL.Inthisstagingsystem,stageIrepresentslocalizeddiseasecontainedwithinalymphnodegroup,IIrepresentsthepresenceoflymphomaintwoormorelymphnodesgroups,IIIrepresentsspreadofthelymphomatolymphnodesgroupsonbothsidesofthediaphragm,andIVindicatesspreadtotissueoutsidethelymphaticsystem.Differentsuffixesimplytheinvolvementofdifferentorgans,forexample,SforthespleenandHfortheliver.Extra-lymphaticinvolvementisexpressedwiththeletterE.Inaddition,thepresenceofBsymptoms(oneormoreofthefollowing:unintentionallossof10%bodyweightinthelast6months,nightsweats,orpersistentfeverof38 °Cormore)ortheirabsenceisexpressedwithBorA,respectively.[43] CTscanorPETscanimagingmodalitiesareusedtostagecancer.PETscanningisadvisedforfluorodeoxyglucose-avidlymphomas,suchasHodgkinlymphoma,asastagingtoolthatcanevenreplacebonemarrowbiopsy.Forotherlymphomas,CTscanningisrecommendedforstaging.[42] Ageandpoorperformancestatusareotherestablishedpoorprognosticfactors.[44]Thismeansthatpeoplewhoareelderlyortoosicktotakecareofthemselvesaremorelikelytodiefromlymphomathanothers. Mantlecelllymphoma:Noticetheirregularnuclearcontoursofthemedium-sizedlymphomacellsandthepresenceofapinkhistiocyte.Byimmunohistochemistry,thelymphomacellsexpressedCD20,CD5,andCyclinD1(high-powerview,H&E) Hodgkinlymphoma,nodularlymphocytepredominant(low-powerview):Noticethenodulararchitectureandtheareasof"mottling".(H&E) Hodgkinlymphoma,nodularlymphocytepredominant(high-powerview):NoticethepresenceofL&Hcells,alsoknownas"popcorncells".(H&E) Differentialdiagnosis[edit] Certainlymphomas(extranodalNK/T-celllymphoma,nasaltypeandtypeIIenteropathy-associatedT-celllymphoma)canbemimickedbytwobenigndiseaseswhichinvolvetheexcessiveproliferationofnon-malignantNKcellsintheGItract,naturalkillercellenteropathy,adiseasewhereinNKcellinfiltrativelesionsoccurintheintestine,colon,stomach,oresophagus,andlymphomatoidgastropathy,adiseasewhereinthesecells'infiltrativelesionsarelimitedtothestomach.Thesediseasesdonotprogresstocancer,mayregressspontaneouslyanddonotrespondto,anddonotrequire,chemotherapyorotherlymphomatreatments.[45] Treatment[edit] PrognosesandtreatmentsaredifferentforHLandbetweenallthedifferentformsofNHL,[46]andalsodependonthegradeoftumour,referringtohowquicklyacancerreplicates.Paradoxically,high-gradelymphomasaremorereadilytreatedandhavebetterprognoses:[citationneeded]Burkittlymphoma,forexample,isahigh-gradetumourknowntodoublewithindays,andishighlyresponsivetotreatment. Low-grade[edit] Manylow-gradelymphomasremainindolent(growingslowlyornotatall)formanyyears–sometimes,fortherestoftheperson'slife.Withanindolentlymphoma,suchasfollicularlymphoma,watchfulwaitingisoftentheinitialcourseofaction,becausemonitoringislessriskyandlessharmfulthanearlytreatment.[47] Ifalow-gradelymphomabecomessymptomatic,radiotherapyorchemotherapyarethetreatmentsofchoice.Althoughthesetreatmentsdonotpermanentlycurethelymphoma,theycanalleviatethesymptoms,particularlypainfullymphadenopathy.Peoplewiththesetypesoflymphomacanlivenear-normallifespans,eventhoughthediseaseistechnicallyincurable. Somecentersadvocatetheuseofsingleagentrituximabinthetreatmentoffollicularlymphomaratherthanthewait-and-watchapproach.Watchfulwaitingisnotadesirablestrategyforeveryone,asitleadstosignificantdistressandanxietyinsomepeople.Ithasbeencalled"watchandworry".[48] High-grade[edit] Treatmentofsomeother,moreaggressive,formsoflymphoma[which?]canresultinacureinthemajorityofcases,buttheprognosisforpeoplewithapoorresponsetotherapyisworse.[49]Treatmentforthesetypesoflymphomatypicallyconsistsofaggressivechemotherapy,includingtheCHOPorR-CHOPregimen.Anumberofpeoplearecuredwithfirst-linechemotherapy.Mostrelapsesoccurwithinthefirsttwoyears,andtherelapseriskdropssignificantlythereafter.[50]Forpeoplewhorelapse,high-dosechemotherapyfollowedbyautologousstemcelltransplantationisaprovenapproach.[51] Thetreatmentofsideeffectsisalsoimportantastheycanoccurduetothechemotherapyorthestemcelltransplantation.Itwasevaluatedwhethermesenchymalstromalcellscanbeusedforthetreatmentandprophylaxisofgraft-versus-hostdiseases.Theevidenceisveryuncertainaboutthetherapeuticeffectofmesenchymalstromalcellstotreatgraft-versus-hostdiseasesontheall-causemortalityandcompletedisappearofchronicacutegraft-versus-hostdiseases.Mesenchymalstromalcellsmayresultinlittletonodifferenceintheall-causemortality,relapseofmalignantdiseaseandincidenceofacuteandchronicgraft-versus-hostdiseasesiftheyareusedforprophylacticreason.[52]Moreover,itwasseenthatplatelettransfusionsforpeopleundergoingachemotherapyorastemcelltransplantationforthepreventionofbleedingeventshaddifferenteffectsonthenumberofparticipantswithableedingevent,thenumberofdaysonwhichableedingoccurred,themortalitysecondarytobleedingandthenumberofplatelettransfusionsdependingonthewaytheywereused(therapeutic,dependingonathreshold,differentdoseschedulesorprophylactic).[53][54] FourchimericantigenreceptorCAR-TcelltherapiesareFDA-approvedfornon-Hodgkinlymphoma,includinglisocabtagenemaraleucel(forrelapsedorrefractorylargeB-celllymphomawithtwofailedsystemictreatments),axicabtageneciloleucel,tisagenlecleucel(forlargeB-celllymphoma),andbrexucabtageneautoleucel(formantlecelllymphoma).Thesetherapiescomewithcertificationandotherrestrictions.[55] Hodgkinlymphoma[edit] Hodgkinlymphomatypicallyistreatedwithradiotherapyalone,aslongasitislocalized.[56] AdvancedHodgkindiseaserequiressystemicchemotherapy,sometimescombinedwithradiotherapy.[57]ChemotherapyusedincludestheABVDregimen,whichiscommonlyusedintheUnitedStates.OtherregimensusedinthemanagementofHodgkinlymphomaincludeBEACOPPandStanfordV.ConsiderablecontroversyexistsregardingtheuseofABVDorBEACOPP.Briefly,bothregimensareeffective,butBEACOPPisassociatedwithmoretoxicity.Encouragingly,asignificantnumberofpeoplewhorelapseafterABVDcanstillbesalvagedbystemcelltransplant.[58] Scientistsevaluatedwhetherpositron-emission-tomographyscansbetweenthechemotherapycyclescanbeusedtomakeassumptionsaboutthesurvival.Theevidenceisveryuncertainabouttheeffectofnegative(=goodprognosis)orpositive(=badprognosis)interimPETscanresultsontheprogression-freesurvival.NegativeinterimPETscanresultsmayresultinanincreaseinprogression-freesurvivalcomparediftheadjustedresultwasmeasured.NegativeinterimPETscanresultsprobablyresultinalargeincreaseintheoverallsurvivalcomparedtothosewithapositiveinterimPETscanresult.[59] CurrentresearchevaluatedwhetherNivolumabcanbeusedforthetreatmentofaHodgkin'slymphoma.TheevidenceisveryuncertainabouttheeffectofNivolumabforpatientswithaHodgkin'slymphomaontheoverallsurvival,thequalityoflife,thesurvivalwithoutaprogression,theresponserate(=completedisappear)andgrade3or4seriousadverseevents.[60] Palliativecare[edit] Palliativecare,aspecializedmedicalcarefocusedonthesymptoms,pain,andstressofaseriousillness,isrecommendedbymultiplenationalcancertreatmentguidelinesasanaccompanimenttocurativetreatmentsforpeoplewithlymphoma.[61][62]Itisusedtoaddressboththedirectsymptomsoflymphomaandmanyunwantedsideeffectsthatarisefromtreatments.[63][64]Palliativecarecanbeespeciallyhelpfulforchildrenwhodeveloplymphoma,helpingbothchildrenandtheirfamiliesdealwiththephysicalandemotionalsymptomsofthedisease.[63][65][66][67]Forthesereasons,palliativecareisespeciallyimportantforpeoplerequiringbonemarrowtransplants.[68][69] Supportivetreatment[edit] Addingphysicalexercisestothestandardtreatmentforadultpatientswithhaematologicalmalignancieslikelymphomasmayresultinlittletonodifferenceinthemortality,thequalityoflifeandthephysicalfunctioning.Theseexercisesmayresultinaslightreductionindepression.Furthermore,aerobicphysicalexercisesprobablyreducefatigue.Theevidenceisveryuncertainabouttheeffectonanxietyandseriousadverseevents.[70]   Prognosis[edit] Five-yearrelativesurvivalbystageatdiagnosis[71] Stageatdiagnosis Five-yearrelativesurvival(%) Percentageofcases(%) Localized(confinedtoprimarysite) 82.3 26 Regional(spreadtoregionallymphnodes) 78.3 19 Distant(cancerhasmetastasized) 62.7 47 Unknown(unstaged) 68.6 8 Epidemiology[edit] Deathsfromlymphomasandmultiplemyelomapermillionpersonsin2012  0-13  14-18  19-22  23-28  29-34  35-42  43-57  58-88  89-121  122-184 Lymphomaisthemostcommonformofhematologicalmalignancy,or"bloodcancer",inthedevelopedworld. Takentogether,lymphomasrepresent5.3%ofallcancers(excludingsimplebasalcellandsquamouscellskincancers)intheUnitedStatesand55.6%ofallbloodcancers.[72] AccordingtotheU.S.NationalInstitutesofHealth,lymphomasaccountforabout5%,andHodgkinlymphomainparticularaccountsforlessthan1%ofallcasesofcancerintheUnitedStates.[citationneeded] Becausethewholelymphaticsystemispartofthebody'simmunesystem,peoplewithaweakenedimmunesystemsuchasfromHIVinfectionorfromcertaindrugsormedicationalsohaveahighernumberofcasesoflymphoma.[73] History[edit] ThomasHodgkin ThomasHodgkinpublishedthefirstdescriptionoflymphomain1832,specificallyoftheformnamedafterhim.[74]Sincethen,manyotherformsoflymphomahavebeendescribed. Theterm"lymphoma"isfromLatinlympha("water")andfromGreek-oma("morbidgrowth,tumor").[75] Research[edit] Thetwotypesoflymphomaresearchareclinicalortranslationalresearchandbasicresearch.Clinical/translationalresearchfocusesonstudyingthediseaseinadefinedandgenerallyimmediatelyapplicableway,suchastestinganewdruginpeople.Studiesmayfocusoneffectivemeansoftreatment,betterwaysoftreatingthedisease,improvingthequalityoflifeforpeople,orappropriatecareinremissionoraftercures.Hundredsofclinicaltrialsarebeingplannedorconductedatanygiventime.[76] Basicscienceresearchstudiesthediseaseprocessatadistance,suchasseeingwhetherasuspectedcarcinogencancausehealthycellstoturnintolymphomacellsinthelaboratoryorhowtheDNAchangesinsidelymphomacellsasthediseaseprogresses.Theresultsfrombasicresearchstudiesaregenerallylessimmediatelyusefultopeoplewiththedisease,[77]butcanimprovescientists'understandingoflymphomaandformthefoundationforfuture,moreeffectivetreatments. 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Externallinks[edit] LymphomaatCurlie ClassificationDICD-10:C81–C96ICD-9-CM:202.8ICD-O:9590–9999MeSH:D008223ExternalresourcesMedlinePlus:000580 Authoritycontrol:Nationallibraries France(data) Israel UnitedStates Latvia CzechRepublic Retrievedfrom"https://en.wikipedia.org/w/index.php?title=Lymphoma&oldid=1108763779" Categories:LymphomaAnatomicalpathologyHematologyPediatriccancersHiddencategories:CS1errors:missingperiodicalCS1maint:archivedcopyastitleCS1maint:bot:originalURLstatusunknownArticleswithshortdescriptionShortdescriptionmatchesWikidataShortdescriptionisdifferentfromWikidataAllarticleswithunsourcedstatementsArticleswithunsourcedstatementsfromNovember2021ArticleswithunsourcedstatementsfromJuly2013Allarticleswithspecificallymarkedweasel-wordedphrasesArticleswithspecificallymarkedweasel-wordedphrasesfromJuly2013ArticleswithCurlielinksArticleswithBNFidentifiersArticleswithJ9UidentifiersArticleswithLCCNidentifiersArticleswithLNBidentifiersArticleswithNKCidentifiersWikipediamedicinearticlesreadytotranslate Navigationmenu Personaltools NotloggedinTalkContributionsCreateaccountLogin Namespaces ArticleTalk English Views ReadEditViewhistory More Search Navigation MainpageContentsCurrenteventsRandomarticleAboutWikipediaContactusDonate Contribute HelpLearntoeditCommunityportalRecentchangesUploadfile Tools WhatlinkshereRelatedchangesUploadfileSpecialpagesPermanentlinkPageinformationCitethispageWikidataitem Print/export DownloadasPDFPrintableversion Inotherprojects WikimediaCommons Languages العربيةঅসমীয়াAsturianuAzərbaycancaБългарскиBosanskiCatalàČeštinaDanskDeutschދިވެހިބަސްΕλληνικάEspañolEuskaraفارسیFrançaisGaeilgeGalego한국어ՀայերենHrvatskiBahasaIndonesiaInterlinguaItalianoעבריתКыргызчаLatinaLatviešuLietuviųМакедонскиമലയാളംBahasaMelayuNederlandsनेपालभाषा日本語Norskbokmålଓଡ଼ିଆPolskiPortuguêsRomânăРусскийSimpleEnglishSlovenščinaСрпски/srpskiSrpskohrvatski/српскохрватскиSuomiSvenskaதமிழ்Татарча/tatarçaไทยTürkçeУкраїнськаVahcuenghTiếngViệt粵語中文 Editlinks



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