Influence of BCR-ABL Transcript Type on Outcome in Patients with Chronic-Phase Chronic Myeloid Leukemia Treated with Imatinib

Abstract Background The prognostic significance of BCR-ABL1 transcripts in chronic myeloid leukemia (CML) is still controversial. Methods All consecutive CML patients in chronic phase treated with imatinib in a single center were analyzed (n=170). BCR-ABL1 transcript was evaluated by multiplex RT-PC...

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Published inClinical lymphoma, myeloma and leukemia Vol. 17; no. 11; pp. 728 - 733
Main Authors Pagnano, Katia Borgia Barbosa, Miranda, Eliana Cristina, Delamain, Márcia Torresan, Duarte, Gislaine Oliveira, de Paula, Erich Vinicius, Lorand-Metze, Irene, de Souza, Carmino Antonio
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.11.2017
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Summary:Abstract Background The prognostic significance of BCR-ABL1 transcripts in chronic myeloid leukemia (CML) is still controversial. Methods All consecutive CML patients in chronic phase treated with imatinib in a single center were analyzed (n=170). BCR-ABL1 transcript was evaluated by multiplex RT-PCR. Exclusively patients with BCR-ABL transcripts e13a2 and/or e14a2 were included in this analysis. Results Patients with e14a2 transcripts presented higher rates of optimal molecular responses at 3 months and higher rates of CCyR at 6 months. E13a2, e14a2 and e14a2+e13a2 groups presented similar rates of 5-year event-free, progression-free and overall survival. There was a superior 10-year overall survival in patients with transcripts e13a2 compared to e14a2 (alone or coexpressed with e13a2) (93% vs. 73%, P=0.03), although the 5-year overall survival was 96% vs. 88%, respectively (P=NS). In a multivariate analysis, high/intermediate Sokal score and e14a3/e14a3+e14a2 were independent factors for poor overall survival (HR= 4.63, P=0.023 for Sokal score and HR= 10.6, 0.041 for BCR-ABL transcript). Conclusions Patients with BCR-ABL transcripts e14a2 transcripts have higher rates of CCyR at 6 months and higher rates of optimal molecular response at 3 months when compared to e13a2 or to both transcripts, but no difference in 5-year overall, progression-free and event-free survival. There was a superior 10-year overall survival among patients with transcripts e13a2 compared to e14a2 (alone or coexpressed with e13a2).
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ISSN:2152-2650
2152-2669
DOI:10.1016/j.clml.2017.06.009