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Gender and BCR-ABL transcript type are correlated with molecular response to imatinib treatment in patients with chronic myeloid leukemia.
Lin, Han-Xin; Sjaarda, Jenny; Dyck, Jocob; Stringer, Randa; Hillis, Chris; Harvey, Maria; Carter, Ronald; Ainsworth, Peter; Leber, Brian; Pare, Guillaume; Sadikovic, Bekim.
Afiliação
  • Lin HX; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Sjaarda J; Hamilton Regional Laboratory Medicine Program, Hamilton Health Science, Hamilton, ON, Canada.
  • Dyck J; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Stringer R; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Hillis C; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Harvey M; Department of Oncology, McMaster University, Juravinski Hospital, Hamilton, ON, Canada.
  • Carter R; Hamilton Regional Laboratory Medicine Program, Hamilton Health Science, Hamilton, ON, Canada.
  • Ainsworth P; Department of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
  • Leber B; Hamilton Regional Laboratory Medicine Program, Hamilton Health Science, Hamilton, ON, Canada.
  • Pare G; Department of Pathology and Laboratory Medicine, Western University, London, ON, Canada.
  • Sadikovic B; Molecular Genetics Laboratory, London Health Sciences Centre, London, ON, Canada.
Eur J Haematol ; 96(4): 360-6, 2016 Apr.
Article em En | MEDLINE | ID: mdl-26059983
ABSTRACT

OBJECTIVES:

Achieving a major molecular response (MMR) is the goal of imatinib therapy for chronic myeloid leukemia. However, the association between gender, BCR-ABL transcript type, and age with MMR is not well understood and often controversial.

METHODS:

We retrospectively analyzed 166 patients who have been treated with imatinib for up to 10 yr.

RESULTS:

Men had a lower MMR rate than women (63.3% vs. 81.6%, P = 0.006) and a shorter time to relapse (median 354 vs. 675 d, P = 0.049), while patients with b3a2 or with both b3a2 and b2a2 break point transcripts had higher MMR rate than those with b2a2 (81.8%, 77.1% vs. 60.7%, P = 0.023 for b3a2 vs. b2a2, P = 0.043 for both vs. b2a2). A striking difference was found between men with b2a2 and women with both b2a2 and b3a2 in terms of MMR rate (43.8% vs. 88.9%), MMR rate within 6 months (7.1% vs. 62.5%) and the time to MMR (median d 493 vs. 159, P = 0.036).

CONCLUSIONS:

Both gender and BCR-ABL transcript, but not age, were significantly associated with the molecular response. Men with b2a2 represent a less favorable group in their response to imatinib treatment and may need alternative therapy regimen and closer monitoring.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Leucemia Mielogênica Crônica BCR-ABL Positiva / Proteínas de Fusão bcr-abl / Inibidores de Proteínas Quinases / Mesilato de Imatinib / Antineoplásicos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: RNA Mensageiro / Leucemia Mielogênica Crônica BCR-ABL Positiva / Proteínas de Fusão bcr-abl / Inibidores de Proteínas Quinases / Mesilato de Imatinib / Antineoplásicos Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2016 Tipo de documento: Article