Pretherapeutic Expression of the hOCT1 Gene Predicts a Complete Molecular Response to Imatinib Mesylate in Chronic-Phase Chronic Myeloid Leukemia
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
17/09/2013
17/09/2013
01/08/2012
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Resumo |
In this retrospective study we evaluated the pretherapeutic mRNA expression of the hOCT1 (human organic cation transporter 1) gene in patients with chronic-phase (CP) chronic myeloid leukemia (CML) who varied in terms of their response to imatinib (IM). hOCT1 mRNA was quantified by real-time PCR. Patients were classified as expressing either high (n = 44) or low hOCT1 mRNA (n = 44). The complete cytogenetic response rates observed at 6, 12 and 18 months were 47.7, 84.1 and 91%, respectively, in patients with high hOCT1 mRNA and 47.5, 81.8 and 86.3%, respectively, in patients with low hOCT1 transcripts. The major molecular response rates were not significantly different between patients with high and low hOCT1 mRNA after 6 months of therapy (22.7 vs. 9.1%; p = 0.07), but they were significantly different after 12 months (54.5 vs. 31.8%; p = 0.026) and 18 months (77.2 vs. 56.8%; p = 0.034). Complete molecular responses were observed in 5 patients with low and 17 patients with high hOCT1 mRNA (p = 0.003). The 5-year event-free and overall survival analyses revealed no significant differences between the groups. These data imply that knowledge of the pretherapeutic level of hOCT1 could be a useful marker to predict IM therapy outcome in treatment-naive CP CML patients. Copyright (C) 2012 S. Karger AG, Basel Maria Cecilia Souto Vidigal Foundation, Sao Paulo, Brazil Maria Cecilia Souto Vidigal Foundation, Sao Paulo, Brazil |
Identificador |
ACTA HAEMATOLOGICA, BASEL, v. 127, n. 4, pp. 228-234, AUG, 2012 0001-5792 http://www.producao.usp.br/handle/BDPI/33424 10.1159/000336610 |
Idioma(s) |
eng |
Publicador |
KARGER BASEL |
Relação |
ACTA HAEMATOLOGICA |
Direitos |
restrictedAccess Copyright KARGER |
Palavras-Chave | #CHRONIC MYELOID LEUKEMIA #HOCT1 GENE #IMATINIB #CHRONIC MYELOGENOUS LEUKEMIA #ABL TYROSINE KINASE #ACUTE LYMPHOBLASTIC-LEUKEMIA #BCR-ABL #DRUG-RESISTANCE #OCT-1 ACTIVITY #INHIBITOR #CELLS #THERAPY #MUTATIONS #HEMATOLOGY |
Tipo |
article original article publishedVersion |