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rev bras hematol hemoter. 2017;39(4):299–300

w w w . r b h h . o r g

Revista

Brasileira

de

Hematologia

e

Hemoterapia

Brazilian

Journal

of

Hematology

and

Hemotherapy

Scientific

Comment

Hodgkin’s

lymphoma

in

developing

countries:

can

we

go

further?

Rafael

Dezen

Gaiolla

UniversidadeEstadual“JúliodeMesquitaFilho”(UNESP),Botucatu,SP,Brazil

Hodgkin’slymphoma(HL)isaBcellmalignancythataffects approximately 8000 new patients in the United States annually.1 This is the most common lymphoma affecting

theyoungpopulationwithahigherincidenceatages15to 35years.Becauseofitsparticularhistologicalfeaturesand biologicalbehavior,HLishighlyresponsivetochemotherapy andradiation,andthereforeisconsideredamodelof success-fulcancertreatment.Infact,inthelastdecades,important advances were made regarding HL treatment resulting in unprecedented high cure rates. Elegantly designed clinical trialsconductedbyimportantcooperativegroupsinEurope andNorthAmericahavesetthebasisfortreatmentand estab-lishedtheguidelinesforHLmanagementinthemodernera. Inearly-stagedisease,treatmentbasedontheABVD (Doxoru-bicin,Bleomycin,Vinblastine,Dacarbazine)regimenremains thestandardofcare.Short-coursechemotherapy(2–4cycles) followedbyradiotherapy (20–30Gy) hasdemonstrated high efficacy and acceptable acute and long-term toxicity, with cureratesthatexceed90%.2Durationoftreatmentanddoses

ofradiationdependonthepresenceofsomeadverse prognos-ticfactors.3Inadvanced-stageHL,thebesttreatmentchoice

hasbeenamatterofexhaustivedebate.IntheUnitedStates, 6–8cyclesofABVDremainsthestandardofcare,resultingin 5-yearfailure-freesurvivalof60%and5-yearOSof73%.4,5In

Europe,theGerman HodgkinStudyGrouphas developeda moreintensiveprotocol,theescalatedBEACOPP(bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine,

DOIoforiginalarticle:http://dx.doi.org/10.1016/j.bjhh.2017.08.001.

SeepaperbyJaime-Pérezetal.onpages325–30.

Correspondenceto:HospitaldasClínicasdaFaculdadedeMedicinadeBotucatudaUniversidadeEstadual“JúliodeMesquitaFilho”

(HCFMB-UNESP),DistritodeRubiãoJuniorS/N,Botucatu,SP,Brazil. E-mailaddress:[email protected]

procarbazine,andprednisone)regimen,whichiswidelyused inmany centers.When comparedtoABVD,escalated BEA-COPP resultsinbetterprogression-freeand overallsurvival but withmore acute and late toxicities.6–8 Defining which

patientsreallydobenefitfrommoreintensiveregimensisstill achallenge.9Morerecently,theconceptofresponse-adapted

therapy based on interim positron emission tomography-computedtomography(PET-CT)hasproventobeofprognostic importanceand seemstoimprove outcomesbyidentifying patients who are most likelyto benefit from morepotent treatmentregimens.10

In developing countries, however, the outcomes of HL treatment are notsoexciting. Althoughdataisscarce and mostly comes from small population-based and retrospec-tivestudies,thereportedprogression-freesurvivalandoverall survivalaresignificantlylowerthanthoseobservedin devel-opedcountries,especiallyforadvanced-stagedisease.11,12In

this issue of the Revista Brasileira de Hematologia e Hemoter-apia,Jaime-Pérezetal.13presentthedataof128HLpatients

retrospectivelystudiedatauniversityhospitalinMonterrey, Mexico.Theauthorsfoundahighrateofprimaryrefractory disease(43%oftheentirecohort)andpoor5-year progression-freesurvival(PFS)evenfortheearly-stagepopulation(median: 42.7%; 95% confidence interval: 27.5–57.9).Noteworthy, the majorityofpatientspresentedwithadvanceddiseaseandup to20%experiencedchemotherapydosereductionsdueto tox-icityordidnotcompletetheplanedtreatment.Somerobust

http://dx.doi.org/10.1016/j.bjhh.2017.08.004

(2)

300

revbrashematolhemoter.2017;39(4):299–300

datahasrecentlybeen publishedbythe Brazilian Prospec-tiveHodgkin’sLymphomaRegistry,14similarlyshowingahigh

proportionofadvanced-stageHLatthemomentof diagno-sisinBrazil.However,the3-yearPFSandoverallsurvival(OS) were74%and90%,respectively,betterthan thoseobserved intheMexicanstudy.Withsmalldifferences,similarfindings have been observed inother developing countries.11,12,15,16

Altogether,thesedatasuggestthatoutcomesofHLtreatment areveryheterogeneousacrossdifferentregionsoftheworld. Onepossibleexplanationisthatinmanydevelopingcountries patients may not have easy access to public healthcare, whichcouldpostponediagnosisandincreasethenumberof moreadvanced-stageHL.Oncediagnosed,patientsnotalways havefullaccesstoadequatestagingprocedures(even com-puted tomography), resulting in a considerable number of under staged and,therefore, undertreated cases. Addition-ally,somehospitalsnotalwayshaveappropriateemergency supportive careto deal with chemotherapy complications, therebyincreasingmorbidityandmortalityrates.Finally, dif-ferences in the economic and social environment, pattern ofEpstein–Barrvirusinfectionandgeneticbackgroundmay alsoexplainsomedifferencesinHLbehavioratdifferent geo-graphiclocations.17Indeed,lowereconomicstatushasbeen

associatedwithmoreaggressivediseaseandworseoutcomes inHL.18

AlthoughJaime-Pérezetal.describedasingleinstitution experience,theirworkbringsintofocusaveryimportant con-cernaboutthemanagementofHLincountrieswithlimited resources.Alltheeffortsnecessarytoimprovediagnosisand treatmentoutcomesareofextremeimportanceandstrongly desirableinthecontextofahighlycurabledisease.

Conflicts

of

interest

Theauthordeclaresnoconflictofinterest

r

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f

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r

e

n

c

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s

1. NationalCancerInstituteSurveillance.Epidemiology,and EndResults(SEER)ProgramPopulations(1969–2015).DCCPS, SurveillanceResearchProgram,releasedDecember;2016. Availablefrom:www.seer.cancer.gov/popdata

2. EngertA,PlütschowA,EichHT,LohriA,DörkenB,

BorchmannP,etal.Reducedtreatmentintensityinpatients

withearly-stageHodgkin’slymphoma.NEnglJMed.

2010;363(7):640–52.

3. EichHT,DiehlV,GorgenH,PabstT,MarkovaJ,DebusJ,etal.

Intensifiedchemotherapyanddose-reducedinvolved-field

radiotherapyinpatientswithearlyunfavorableHodgkin’s

lymphoma:finalanalysisoftheGermanHodgkinStudy

GroupHD11trial.JClinOncol.2010;28(27):4199–206.

4. VivianiS,BonadonnaG,SantoroA,BonfanteV,ZaniniM,

DevizziL,etal.AlternatingversushybridMOPPandABVD

combinationsinadvancedHodgkin’sdisease:ten-year

results.JClinOncol.1996;14(5):1421–30.

5. DugganDB,PetroniGR,JohnsonJL,GlickJH,FisherRI,

ConnorsJM,etal.RandomizedcomparisonofABVDand

MOPP/ABVhybridforthetreatmentofadvancedHodgkin’s

disease:reportofanintergrouptrial.JClinOncol.

2003;21(4):607–14.

6.EngertA,DiehlV,FranklinJ,LohriA,DörkenB,LudwigW-D,

etal.Escalated-doseBEACOPPinthetreatmentofpatients

withadvanced-stageHodgkin’slymphoma:10yearsof

follow-upoftheGHSGHD9study.JClinOncol.

2009;27(27):4548–54.

7.EngertA,HaverkampH,KobeC,MarkovaJ,RennerC,HoA,

etal.Reduced-intensitychemotherapyandPET-guided

radiotherapyinpatientswithadvancedstageHodgkin’s

lymphoma(HD15trial):arandomised,open-label,phase3

non-inferioritytrial.Lancet.2012;379(9828):1791–9.

8.SkoetzN,WillA,MonsefI,BrillantC,EngertA,vonTresckow B.Comparisonoffirst-linechemotherapyincludingescalated BEACOPPversuschemotherapyincludingABVDforpeople withearlyunfavourableoradvancedstageHodgkin

lymphoma.In:TheCochraneCollaboration,editor.Cochrane DatabaseofSystematicReviews[Internet].JohnWiley&Sons, Ltd.;2017.Availablefrom:

http://doi.wiley.com/10.1002/14651858.CD007941.pub3[cited

27.8.17].

9.VassilakopoulosTP,JohnsonPW.Treatmentof

advanced-stageHodgkinlymphoma.SeminHematol.

2016;53(3):171–9.

10.MoghbelMC,MittraE,GallaminiA,NiederkohrR,ChenDL,

ZukotynskiK,etal.Responseassessmentcriteriaandtheir

applicationsinlymphoma:Part2.JNuclMed.

2017;58(1):13–22.

11.MaddiRN,LingaVG,IyerKK,ChowdaryJS,GundetiS,

DigumartiR,etal.Clinicalprofileandoutcomeofadult

Hodgkinlymphoma:experiencefromatertiarycare

institution.IndianJMedPaediatrOncol.2015;36(4):255–60.

12.ChatenoudL,BertuccioP,BosettiC,RodriguezT,LeviF,Negri

E,etal.Hodgkin’slymphomamortalityintheAmericas,

1997–2008:achievementsandpersistentinadequacies:

Hodgkin’slymphomamortalityintheAmericas.IntJCancer.

2013;133(3):687–94.

13.Jaime-PérezJC,Gamboa-AlonsoCM,Padilla-MedinaJR,

Jiménez-CastilloRA,Olguín-RamírezLA,Gutiérrez-Aguirre

CH,etal.Highfrequencyofprimaryrefractorydiseaseand

lowprogression-freesurvivalrateofHodgkinlymphoma:a

decadeofexperienceinaLatinAmericancenter.RevBras

HematolHemoter.2017;39(4):325–30.

14.BiasoliI,CastroN,DelamainM,SilveiraT,FarleyJ,SimõesBP,

etal.TreatmentoutcomesforHodgkinlymphoma:firstreport

fromtheBrazilianProspectiveRegistry.HematolOncol.2017

(aheadofprint).

15.AndjelicB,AnticD,JakovicL,TodorovicM,BogdanovicA,

DjurasinovicV,etal.Asingleinstitutionexperienceon314

newlydiagnosedadvancedHodgkinlymphomapatients:the

roleofABVDindailypractice.EurJHaematol.

2014;93(5):392–9.

16.ShafiRG,Al-MansourMM,KanfarSS,AlHashmiH,AlsaeedA,

Al-FoheidiM,etal.Hodgkinlymphomaoutcome:a

retrospectivestudyfrom3tertiarycentersinSaudiArabia.

OncolResTreat.2017;40(5):288–92.

17.HoppeRT,MauchPT,ArmitageJO,DiehlV,WeissLM.Hodgkin

Lymphoma.2nded.Philadelphia;1999.

18.BiasoliI,CastroN,DelamainM,SilveiraT,FarleyJ,SimõesBP,

etal.Lowersocioeconomicstatusisassociatedwithshorter

survivalinHLpatients–ananalysisfromtheBrazilian

HodgkinLymphomaRegistry.Cologne,Germany:Poster

presentedat:10thinternationalSymposiumonHodgkin

Referências

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