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Vol. 39. Núm. 3.Julho - Setembro 2017
Páginas 187-292
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Vol. 39. Núm. 3.Julho - Setembro 2017
Páginas 187-292
Scientific Comment
DOI: 10.1016/j.bjhh.2017.05.005
Open Access
BCR-ABL1 level monitoring in chronic myeloid leukemia by real time polymerase chain reaction in Brazil – not so real
Katia Borgia Barbosa Pagnano
Autor para correspondência

Corresponding author at: Centro de Hematologia e Hemoterapia, Universidade Estadual de Campinas (Unicamp), Rua Carlos Chagas 480, Cidade Universitária Zeferino Vaz, 13092-801 Campinas, SP, Brazil. Tel.: +55 19 35218740.
Universidade Estadual de Campinas (Unicamp), Campinas, SP, Brazil
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Rev Bras Hematol Hemoter 2017;39:210-510.1016/j.bjhh.2017.04.007
Ana Lucia Vieira-Mion, Noemi Farah Pereira, Vaneuza Araujo Moreira Funke, Ricardo Pasquini
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Chronic myeloid leukemia (CML) has been successfully managed since tyrosine kinase inhibitors (TKI) became available. Quantitative monitoring of the percentage of the fusion transcript BCR-ABL1 (breakpoint cluster region – c-Abelson murine leukemia oncogene 1, non-receptor tyrosine kinase) by reverse transcription-quantitative real-time polymerase chain reaction (RQ-PCR) is currently the standard of care after starting TKIs, as recommended by the European Leukemia Net and Associação Brasileira de Hematologia, Hemoterapia e Terapia Cellular (ABHH) guidelines.1,2

The prognostic value of early molecular responses was demonstrated in several trials, in first and second-line scenarios. Patients with BCR-ABL levels >10% at three months have lower rates of overall and progression-free survival and increased risk of disease progression.3–6

The European Leukemia Net recommends RQ-PCR to determine the BCR-ABL1 transcript level on the international scale every three months until a major molecular response (MMR – BCR-ABL ≤0.1%, or MR3.0) has been achieved, then every three to six months.2 Patients with failure of current treatment should switch therapy to avoid disease progression to advanced phases.

More recently, the successful results of international discontinuation trials demonstrated that it is possible to discontinue TKI treatment in approximately 40–50% of patients that achieve stable deep molecular responses.7,8 This kind of approach is not feasible without close monitoring of BCR-ABL levels by RQ-PCR.

The standardization of RQ-PCR is challenging and involves sample exchanges with reference laboratories, equipment, trained staff, reagents and calibrators, all of which have an impact on the cost of the test.9,10 In Brazil, there are not many standardized laboratories able to perform BCR-ABL monitoring and to report the results according to the international scale.

In the current issue of the Revista Brasileira de Hematologia e Hemoterapia, in the article “Molecular response to imatinib mesylate of Brazilian patients with chronic myeloid leukemia”, Mion et al. describe the results of RQ-PCR monitoring in a large group of patients and demonstrate the importance of this test in managing CML patients.11

Unfortunately, RQ-PCR is not widely available for all CML patients in Brazil, where most are treated by the public national health system (SUS). The cost of TKIs is high and paid for by the government. However, RQ-PCR is not reimbursed, and, as a consequence, who will pay the cost? An additional problem is the standardization of laboratories and the distance from many centers to a reference laboratory.

Adequate BCR-ABL monitoring may save costs in CML treatment by allowing changes in treatment before disease progression and allowing for some patients to safely stop treatment at the correct point in time. But so far, it is not a reality for most CML patients in Brazil.

Conflicts of interest

The author declares no conflicts of interest

M. Baccarani,M.W. Deininger,G. Rosti,A. Hochhaus,S. Soverini,J.F. Apperley
European LeukemiaNet recommendations for the management of chronic myeloid leukemia: 2013
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Rev Bras Hematol Hemoter, 34 (2012), pp. 367-382
S. Branford,D.W. Kim,S. Soverini,A. Haque,Y. Shou,R.C. Woodman
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Early molecular and cytogenetic response is predictive for long-term progression-free and overall survival in chronic myeloid leukemia (CML)
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Blood, 120 (2012), pp. 1675
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BCR-ABL1 transcript levels at 3 and 6 months are better for identifying chronic myeloid leukemia patients with poor outcome in response to second-line second-generation tyrosine kinase inhibitors after imatinib failure: a report from a single institution
Acta Haematol, 134 (2015), pp. 248-254
D.M. Ross,S. Branford,J.F. Seymour,A.P. Schwarer,C. Arthur,D.T. Yeung
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G. Etienne,J. Guilhot,D. Rea,F. Rigal-Huguet,F. Nicolini,A. Charbonnier
Long-term follow-up of the French stop imatinib (STIM1) study in patients with chronic myeloid leukemia
J Clin Oncol, 35 (2017), pp. 298-305
T. Hughes,M. Deininger,A. Hochhaus,S. Branford,J. Radich,J. Kaeda
Monitoring CML patients responding to treatment with tyrosine kinase inhibitors: review and recommendations for harmonizing current methodology for detecting BCR-ABL transcripts and kinase domain mutations and for expressing results
N.C. Cross,H. White,D. Colomer,H. Ehrencrona,L. Foroni,E. Got-tardi
Laboratory recommendations for scoring deep molecular responses following treatment for chronic myeloid leukemia
Leukemia, 29 (2015), pp. 999-1003
A.L. Mion,N.F. Pereira,V.A. Funke,R. Pasquini
Molecular response to imatinib mesylate of Brazilian patients with chronic myeloid leukemia
Rev Bras Hematol Hemoter, 39 (2017), pp. 210-215

See paper by Vieira-Mion et al. on pages 210–5.

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Hematology, Transfusion and Cell Therapy

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