| Literature DB >> 26159458 |
Beatriz Felicio Ribeiro, Bruna Rocha Vergílio, Eliana Cristina Martins Miranda, Maria Helena Almeida, Marcia Torresan Delamain, Rosana Antunes da Silveira, Carmino Antonio de Souza, Dulcinéia Martins Albuquerque, Andrey Dos Santos, Vagner Oliveira Duarte, Gislaine Borba Oliveira-Duarte, Irene Lorand-Metze, Katia Borgia Barbosa Pagnano.
Abstract
Early reduction of BCR-ABL1 transcript levels has been associated with improved outcome in chronic myeloid leukemia (CML) treatment. We evaluated 54 chronic-phase CML patients treated with imatinib who switched therapy to dasatinib (n = 33) or nilotinib (n = 21). BCR-ABL1 transcript levels were measured in peripheral blood using real-time quantitative PCR (RQ-PCR) every 3 months from the start of second-line treatment. Patients with BCR-ABL transcript levels >10% at 3 months and >1% at 6 months had significantly inferior progression-free (PFS) and event-free survival (EFS) than patients with RQ-PCR <10% at 3 months and <1% at 6 months (66 vs. 100%, p = 0.01, and 33 vs. 73%, p = 0.02, respectively). Patients with RQ-PCR <10% at 3 months and >1% at 6 months also had inferior PFS and EFS than patients with RQ-PCR <10% at 3 months and <1% at 6 months (48 vs. 100%, p = 0.002, and 25 vs. 73%, p < 0.0001, respectively). Two measurements of BCR-ABL levels were better than a single one to stratify chronic-phase CML patients as failure after second-line therapy.Entities:
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Year: 2015 PMID: 26159458 DOI: 10.1159/000430835
Source DB: PubMed Journal: Acta Haematol ISSN: 0001-5792 Impact factor: 2.195