• Nenhum resultado encontrado

Rev. Bras. Hematol. Hemoter. vol.39 número3

N/A
N/A
Protected

Academic year: 2018

Share "Rev. Bras. Hematol. Hemoter. vol.39 número3"

Copied!
2
0
0

Texto

(1)

rev bras hematol hemoter. 2017;39(3):197–198

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

Revista

Brasileira

de

Hematologia

e

Hemoterapia

Brazilian

Journal

of

Hematology

and

Hemotherapy

Scientific

Comment

BCR-ABL1

level

monitoring

in

chronic

myeloid

leukemia

by

real

time

polymerase

chain

reaction

in

Brazil

not

so

real

Katia

Borgia

Barbosa

Pagnano

UniversidadeEstadualdeCampinas(Unicamp),Campinas,SP,Brazil

Chronicmyeloidleukemia(CML)hasbeensuccessfully man-agedsincetyrosinekinaseinhibitors(TKI)becameavailable. Quantitativemonitoringofthepercentageofthefusion tran-scriptBCR-ABL1(breakpointclusterregion–c-Abelsonmurine leukemiaoncogene1,non-receptortyrosinekinase)byreverse transcription-quantitativereal-timepolymerase chain reac-tion(RQ-PCR)iscurrentlythestandardofcareafterstarting TKIs,asrecommendedbytheEuropeanLeukemia Netand Associac¸ãoBrasileiradeHematologia,HemoterapiaeTerapia Cel-lular(ABHH)guidelines.1,2

Theprognostic value of early molecular responses was demonstratedinseveraltrials, infirst andsecond-line sce-narios.PatientswithBCR-ABL levels>10% atthreemonths havelowerratesofoverallandprogression-freesurvivaland increasedriskofdiseaseprogression.3–6

TheEuropeanLeukemiaNetrecommendsRQ-PCRto deter-minetheBCR-ABL1transcriptlevelontheinternationalscale everythreemonthsuntilamajormolecularresponse(MMR –BCR-ABL ≤0.1%,or MR3.0)hasbeen achieved,then every

threetosixmonths.2 Patientswithfailureofcurrent

treat-mentshouldswitchtherapytoavoiddiseaseprogressionto advancedphases.

DOIoforiginalarticle:http://dx.doi.org/10.1016/j.bjhh.2017.04.007. 夽

SeepaperbyVieira-Mionetal.onpages210–5.

Correspondingauthorat:CentrodeHematologiaeHemoterapia,UniversidadeEstadualdeCampinas(Unicamp),RuaCarlosChagas480,

CidadeUniversitáriaZeferinoVaz,13092-801Campinas,SP,Brazil.Tel.:+551935218740. E-mailaddress:kborgia@unicamp.br

More recently, the successful results of international discontinuationtrialsdemonstratedthatitispossibleto dis-continueTKItreatmentinapproximately40–50%ofpatients thatachievestabledeepmolecularresponses.7,8Thiskindof

approachisnotfeasiblewithoutclosemonitoringofBCR-ABL levelsbyRQ-PCR.

ThestandardizationofRQ-PCRischallengingandinvolves sample exchanges with reference laboratories, equipment, trainedstaff,reagentsandcalibrators,allofwhichhavean impactonthecostofthetest.9,10InBrazil,therearenotmany

standardizedlaboratoriesabletoperformBCR-ABL monitor-ing andtoreportthe resultsaccording tothe international scale.

In the current issue of the Revista Brasileira de Hema-tologia e Hemoterapia, in the article “Molecular response to imatinibmesylateofBrazilianpatientswithchronicmyeloid leukemia”,Mionetal.describetheresultsofRQ-PCR mon-itoring in a large group of patients and demonstrate the importanceofthistestinmanagingCMLpatients.11

Unfortunately,RQ-PCRisnotwidelyavailableforallCML patients in Brazil, where most are treated by the public nationalhealth system(SUS).ThecostofTKIs ishigh and

http://dx.doi.org/10.1016/j.bjhh.2017.05.005

(2)

198

revbrashematolhemoter.2017;39(3):197–198

paidforbythe government. However,RQ-PCR isnot reim-bursed, and,as aconsequence,who will paythe cost? An additionalproblemisthestandardizationoflaboratoriesand thedistancefrommanycenterstoareferencelaboratory.

Adequate BCR-ABL monitoring may save costs in CML treatmentbyallowingchanges intreatmentbeforedisease progression and allowing for some patients to safely stop treatmentatthecorrectpointintime.Butsofar,itisnota realityformostCMLpatientsinBrazil.

Conflicts

of

interest

Theauthordeclaresnoconflictsofinterest

r

e

f

e

r

e

n

c

e

s

1. BaccaraniM,DeiningerMW,RostiG,HochhausA,SoveriniS,

ApperleyJF,etal.EuropeanLeukemiaNetrecommendations

forthemanagementofchronicmyeloidleukemia:2013.

Blood.2013;122(6):872–84.

2. SouzaCA,PagnanoKB,BenditI,ConchonM,FreitasCM,

CoelhoAM,etal.Chronicmyeloidleukemiatreatment

guidelines:BrazilianAssociationofHematology,

HemotherapyandCellTherapy.BrazilianMedicalAssociation

GuidelinesProject–2012.RevBrasHematolHemoter.

2012;34(5):367–82.

3. BranfordS,KimDW,SoveriniS,HaqueA,ShouY,Woodman

RC,etal.Initialmolecularresponseat3monthsmaypredict

bothresponseandevent-freesurvivalat24monthsin

imatinibresistantorintolerantpatientswithPhiladelphia

chromosomepositivechronicmyeloidleukemiainchronic

phasetreatedwithnilotinib.JClinOncol.2012;30:

4323–9.

4. HanfsteinB,MullerMC,HehlmannR,ErbenP,LausekerM,

FabariusA,etal.Earlymolecularandcytogeneticresponseis

predictiveforlong-termprogression-freeandoverallsurvival

inchronicmyeloidleukemia(CML).Leukemia.

2012;26:2096–102.

5.SaglioG,KantarjianHM,ShahN,JabbourEJ,

Quintas-CardamaA,SteegmannJL,etal.Earlyresponse

(molecularandcytogenetic)andlong-termoutcomesin

newlydiagnosedchronicmyeloidleukemiainchronicphase

(CML-CP):exploratoryanalysisofDASISION3-yeardata.

Blood.2012;120:1675.

6.RibeiroBF,VergílioBR,MirandaEC,AlmeidaMH,Delamain

MT,daSilveiraRA,etal.BCR-ABL1transcriptlevelsat3and6

monthsarebetterforidentifyingchronicmyeloidleukemia

patientswithpooroutcomeinresponsetosecond-line

second-generationtyrosinekinaseinhibitorsafterimatinib

failure:areportfromasingleinstitution.ActaHaematol.

2015;134(4):248–54.

7.RossDM,BranfordS,SeymourJF,SchwarerAP,ArthurC,

YeungDT,etal.Safetyandefficacyofimatinibcessationfor

CMLpatientswithstableundetectableminimalresidual

disease:resultsfromtheTWISTERstudy.Blood.

2013;122(4):515–22.

8.EtienneG,GuilhotJ,ReaD,Rigal-HuguetF,NicoliniF,

CharbonnierA,etal.Long-termfollow-upoftheFrenchstop

imatinib(STIM1)studyinpatientswithchronicmyeloid

leukemia.JClinOncol.2017;35(3):298–305.

9.HughesT,DeiningerM,HochhausA,BranfordS,RadichJ,

KaedaJ,etal.MonitoringCMLpatientsrespondingto

treatmentwithtyrosinekinaseinhibitors:reviewand

recommendationsforharmonizingcurrentmethodologyfor

detectingBCR-ABLtranscriptsandkinasedomainmutations

andforexpressingresults.Blood.2006;108(1):28–37.

10.CrossNC,WhiteH,ColomerD,EhrencronaH,ForoniL,

Got-tardiE,etal.Laboratoryrecommendationsforscoring

deepmolecularresponsesfollowingtreatmentforchronic

myeloidleukemia.Leukemia.2015;29(5):999–1003.

11.MionAL,PereiraNF,FunkeVA,PasquiniR.Molecular

responsetoimatinibmesylateofBrazilianpatientswith

chronicmyeloidleukemia.RevBrasHematolHemoter.

Referências

Documentos relacionados

An Excel spreadsheet was sent to all participating insti- tutions, who were asked to provide the following data: patient’s initials; gender; histologic subtype; date of birth; date

Table 2 – Prevalence of chronic medical conditions in patients with and without iron deficiency anemia in elderly subjects aged 60 years and more. Chronic medical conditions

Know- ing the human leukocyte antigens allele group and haplotype frequencies as well as the linkage disequilibrium between alleles of different human leukocyte antigens loci

The objective of this study was to compare miRNA expression profiles of patients with Binet A chronic lymphocytic leukemia with those of sub- jects with high-count monoclonal

Table 1 – Original and Portuguese version of Blood/Injection Fear Scale and the results of content validity ratio (CVR). estimated for

Results: The cases included were 78 chronic lymphocytic leukemias, three atypical chronic lymphocytic leukemias, six marginal zone lymphomas, 11 splenic marginal zone lym- phomas,

Thrombin generated in the thrombin generation test can be quantified as platelet-rich or platelet-poor plasma using the calibrated automated thrombogram method, which monitors

Nutritional assessment and serum zinc and copper concentration in leukemic children. Garófolo A, Lopez FA,