rev bras hematol hemoter. 2015;37(1):3–4
Revista
Brasileira
de
Hematologia
e
Hemoterapia
Brazilian
Journal
of
Hematology
and
Hemotherapy
w w w . r b h h . o r g
Scientific
comment
Myeloid
leukemia:
are
we
getting
better?
夽
Nelson
Hamerschlak
∗HospitalIsraelitaAlbertEinstein,SãoPaulo,SP,Brazil
a
r
t
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c
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i
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f
o
Articlehistory:
Availableonline21November2014
Thestudy by Callera et al., published in this issue of the
Revista Brasileira de Hematologia e Hemoterapia (RBHH),1
revealsevidence ofacontinuous decrease inthe mortality
rateinadultpatientswithmyeloidleukemias from1994to
2011insoutheastBrazil.Undoubtedly,thisdeclineisrelated
tothebetterunderstandingandtreatmentofchronicmyeloid
leukemia(CML),acutemyeloidleukemia(AML)and
promy-elocyticleukemia(APL, M3).2–4 Thewordsmyeloid retirara
palavraandleukemiarefertoaverywiderangeofdisorders
withvaryingseverityand manifestations.Weaddress here
CML,AMLandAPLmainlytobetterunderstandtheadvances
ineachofthem.
IbelievethatthereisreallyatrendinBraziltofollow
devel-opedcountries which havereported significant changes in
prognosis.Unfortunately,westill experiencemany
difficul-ties,butwehavehadprogressaswell:first,tyrosinekinase
iswidelydistributedtopatientswithCMLinBrazil;second,
thehealthauthoritieshavejustopenedapublicconsultation
aboutAMLtreatment,includingcytogeneticsandthe
recom-mendation forthe useofmolecular testsin thetreatment
protocol;andthird,theresultsoftreatmentsofLPAshow
sub-stantialimprovement.3
Evolution in the treatment of leukemia has greatly
improvedthechancesofcureanddiseasecontrol.Morethan
7500peopledevelopleukemiainthecountrytodayand9000
DOIoforiginalarticle:http://dx.doi.org/10.1016/j.bjhh.2014.11.011.
夽
SeepaperbyCalleraetal.onpages7–11.
∗ Correspondenceto:CentrodePesquisaClínica,InstitutoIsraelitadeEnsinoePesquisaAlbertEinstein,Av.AlbertEinstein,627/520,
05651-901SãoPaulo,SP,Brazil.
E-mailaddress:hamer@einstein.br
people die ofthe disease every year in Brazilaccording to
the National Cancer Institute (INCA). Despite the lethality,
leukemiaisnowacurabletypeofcancer.
Prognosisofleukemiapatientstodayisgenerallygood.CML
iscontrolledwithadailypillandacuteleukemiasarecuredin
50–80%ofcases.In recentyears,greatadvanceshavebeen
made intreatment, including chemotherapy,bone marrow
transplantation and targeted-treatments.2 Theintroduction
oftyrosinekinaseinhibitorsinthetreatmentofCML,which
waspreviouslytreatedwithtransplantation,isanevolution.In
addition,greaterknowledgeofthegeneticsbehindthedisease
leads to betterchoices and individualization of treatment.
These improvements intreatment have increasedchances
ofcureanddiseasecontrol,andbetterqualityoflifeforthe
patients. Hence,themostusedtreatmentforCMLtodayis
targetedtherapywiththedrugsimatinib,dasatinibor
niloti-nib.Thetreatmentmustbecontinuedforlife,ensuringthat
thepersonstaysinremissionwhiletakingthedrugs.Thisis
calledfunctionalcure.2
For acute cases, treatment is planned in stages. First
chemotherapyisproposed,usuallywithagood resultfora
shorttime.Thereisaneedtoprovideapostremission
ther-apy.Duringthisperiod,certaincombineddrugsareusedto
extend and maintaindisease remission. In AML,the main
inductionregimen(3+7)hasbeenusedformorethan40years.
http://dx.doi.org/10.1016/j.bjhh.2014.11.006
1516-8484/©2014Associac¸ãoBrasileiradeHematologia,HemoterapiaeTerapiaCelular.PublishedbyElsevierEditoraLtda.Allrights
4
revbrashematolhemoter.2015;37(1):3–4Forcaseswithgoodprognosis,consolidationchemotherapy
orautologoustransplantationhasbeenused.Forcaseswith
badprognosisorwhenrelapseoccurs,allogeneicbone
mar-rowtransplantshavebroughtgoodresults.Theseprocedures
todayareverysafeandrecommended.3
Thus,acytogeneticevaluationthataddressestheso-called
molecular factors, in particular FMS-like tyrosine kinase-3
(FLT3),nucleophosmin(NPM1)andCantharidin-binding
pro-tein(CBP)alphasubunit,isessential,astheyallocatepatients
toreceive consolidationwith chemotherapyand/or
autolo-goustransplants,whenprognosisisfavorable,ortoundergo
allogeneictransplantsincasesofpoorprognosis.Properuse
ofalgorithmsimprovesprognosis.3
Elderlypatients,amongwhomleukemiaismoreprevalent,
startedtobetreatedmoreaggressively,justlikeyoung
peo-ple,becausetheinfrastructureofcarehasimprovedgreatlyin
recentyears.Thisyieldsahighrateofremissionand,inthose
patientswithbetterperformancestatusand lower ratesof
fragility,thepossibilityofundergoinglowtoxicity,allogeneic,
non-myeloablativetransplantation.Data from ourgroup in
partnershipwithMDAndersonHospitalshowresultsinthe
elderlysimilartothoseobtainedwithyoungerpatients.5
Fur-thermore,theadventofhypomethylatingagentsopensnew
perspectivesforthetreatmentofAMLinelderlypatients.6–8
Finally,theeffortinBraziltoimprovethecareofpatients
withAPL throughthe programheadedbyDr.Eduardo Rego
usingaBrazilianprotocolbasedonthatoftheSpanishgroup
(PETHEMA),broughtouroutcomesuptointernationallevels.4
Forallthat,hopefully,inafewyears,myeloidleukemiaswill
becurablediseases
Conflicts
of
interest
Theauthordeclaresnoconflictsofinterest
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2015;37(1):7–11.
2.CortesJ,DeSouzaC,Ayala-SanchezM,BenditI,Best-Aguilera C,EnricoA,etal.Currentpatientmanagementofchronic myeloidleukemiainLatinAmerica:astudybytheLatin AmericanLeukemiaNet(LALNET).Cancer.
2010;116(21):4991–5000.
3.SillaLM,DulleyF,SaboyaR,PatonE,KerbauyF,ArantesAde M,etal.Bonemarrowtransplantationandacuteleukemia: Brazilianguidelines.RevBrasHematolHemoter.
2013;35(1):56–61.
4.RegoEM,KimHT,Ruiz-ArgüellesGJ,UndurragaMS,Uriarte MdelR,JacomoRH,etal.Improvingacutepromyelocytic leukemia(APL)outcomeindevelopingcountriesthrough networking,resultsoftheInternationalConsortiumonAPL. Blood.2013;121(11):1935–43.
5.AlatrashG,deLimaM,HamerschlakN,PelosiniM,WangX, XiaoL,etal.Myeloablativereduced-toxicityi.v.
busulfan-fludarabineandallogeneichematopoieticstemcell transplantforpatientswithacutemyeloidleukemiaor myelodysplasticsyndromeinthesixththrougheighthdecades oflife.BiolBloodMarrowTransplant.2011;17(10):1490–6.
6.KirschbaumM,GojoI,GoldbergSL,BredesonC,KujawskiLA, YangA,etal.Aphase1studyofvorinostatincombination withdecitabineinpatientswithacuteleukaemiaor
myelodysplasticsyndrome.BrJHaematol.2014[Epubaheadof print].
7.MalikP,CashenAF.Decitabineinthetreatmentofacute myeloideleukemiainelderlypatients.CancerManagRes. 2014;6:53–61.