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Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia

To investigate the association of 3- and 6-month BCR-ABL transcript levels on the international scale (BCR-ABL(IS)) and other factors with deep molecular response (DMR) achievement in chronic myeloid leukemia (CML)-chronic phase (CP) patients receiving tyrosine kinase inhibitor (TKI) therapy. We ret...

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Autores principales: Wang, Rui, Cong, Yue, Li, Caili, Zhang, Chen, Lin, Hai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485861/
https://www.ncbi.nlm.nih.gov/pubmed/30985724
http://dx.doi.org/10.1097/MD.0000000000015222
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author Wang, Rui
Cong, Yue
Li, Caili
Zhang, Chen
Lin, Hai
author_facet Wang, Rui
Cong, Yue
Li, Caili
Zhang, Chen
Lin, Hai
author_sort Wang, Rui
collection PubMed
description To investigate the association of 3- and 6-month BCR-ABL transcript levels on the international scale (BCR-ABL(IS)) and other factors with deep molecular response (DMR) achievement in chronic myeloid leukemia (CML)-chronic phase (CP) patients receiving tyrosine kinase inhibitor (TKI) therapy. We retrospectively analyzed the clinical data of 206 patients enrolled in our hospital between January 2010 and July 2018. These patients were initially diagnosed with CML-CP and received imatinib or nilotinib therapy. Early molecular response (EMR) was assessed based on BCR-ABL(IS) (IS: on the international scale) transcript level at 3 and 6 months. Potential factors impacting DMR achievement were identified using Cox proportional hazard regression models. The effects of EMR achievement on the cumulative incidence of MR4.0 were investigated via Kaplan–Meier analysis. Multivariate Cox regression analysis showed that a BCR-ABL(IS) transcript level at 3 and 6 months of TKI therapy was an independent factor for the achievement of MR4.0, which was nevertheless not related to age, gender, Sokal score, hemoglobin level, or white blood cell (WBC) count at the initial time of diagnosis. Patients achieving an EMR (EMR: 3-month BCR-ABL(IS) ≤10%, 6-month BCR-ABL(IS) <1%) were more likely to reach MR4.0 than patients failing to achieve EMR (P(1) <.001, P(2) <.001). Patients who had 3-month BCR-ABL(IS) ≤1% were more likely to reach MR4.0 than those who had 3-month BCR-ABL(IS) of 1% to 10% or >10% (P(1) = .001, P(2) <.001). Similarly, patients who had 6-month BCR-ABL(IS) ≤0.1% were more likely to achieve MR4.0 than those in the 0.1% to 1% and ≥1% groups (P(1) <.001, P(2) <.001). Also, a higher percentage of patients on nilotinib therapy achieved EMR compared with patients on imatinib therapy (93.3% vs 63.6% on 3-month nilotinib therapy, P = .001; 88.9% vs 59.9% on 6-month nilotinib therapy, P = .004). This study demonstrates that EMR, especially a 3-month BCR-ABL(IS) ≤1% and 6-month BCR-ABL(IS) ≤0.1%, have predictive value for DMR achievement. In addition, there is a higher percentage of patients receiving nilotinib therapy achieved EMR than that of those receiving imatinib therapy.
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spelling pubmed-64858612019-05-29 Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia Wang, Rui Cong, Yue Li, Caili Zhang, Chen Lin, Hai Medicine (Baltimore) Research Article To investigate the association of 3- and 6-month BCR-ABL transcript levels on the international scale (BCR-ABL(IS)) and other factors with deep molecular response (DMR) achievement in chronic myeloid leukemia (CML)-chronic phase (CP) patients receiving tyrosine kinase inhibitor (TKI) therapy. We retrospectively analyzed the clinical data of 206 patients enrolled in our hospital between January 2010 and July 2018. These patients were initially diagnosed with CML-CP and received imatinib or nilotinib therapy. Early molecular response (EMR) was assessed based on BCR-ABL(IS) (IS: on the international scale) transcript level at 3 and 6 months. Potential factors impacting DMR achievement were identified using Cox proportional hazard regression models. The effects of EMR achievement on the cumulative incidence of MR4.0 were investigated via Kaplan–Meier analysis. Multivariate Cox regression analysis showed that a BCR-ABL(IS) transcript level at 3 and 6 months of TKI therapy was an independent factor for the achievement of MR4.0, which was nevertheless not related to age, gender, Sokal score, hemoglobin level, or white blood cell (WBC) count at the initial time of diagnosis. Patients achieving an EMR (EMR: 3-month BCR-ABL(IS) ≤10%, 6-month BCR-ABL(IS) <1%) were more likely to reach MR4.0 than patients failing to achieve EMR (P(1) <.001, P(2) <.001). Patients who had 3-month BCR-ABL(IS) ≤1% were more likely to reach MR4.0 than those who had 3-month BCR-ABL(IS) of 1% to 10% or >10% (P(1) = .001, P(2) <.001). Similarly, patients who had 6-month BCR-ABL(IS) ≤0.1% were more likely to achieve MR4.0 than those in the 0.1% to 1% and ≥1% groups (P(1) <.001, P(2) <.001). Also, a higher percentage of patients on nilotinib therapy achieved EMR compared with patients on imatinib therapy (93.3% vs 63.6% on 3-month nilotinib therapy, P = .001; 88.9% vs 59.9% on 6-month nilotinib therapy, P = .004). This study demonstrates that EMR, especially a 3-month BCR-ABL(IS) ≤1% and 6-month BCR-ABL(IS) ≤0.1%, have predictive value for DMR achievement. In addition, there is a higher percentage of patients receiving nilotinib therapy achieved EMR than that of those receiving imatinib therapy. Wolters Kluwer Health 2019-04-12 /pmc/articles/PMC6485861/ /pubmed/30985724 http://dx.doi.org/10.1097/MD.0000000000015222 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Wang, Rui
Cong, Yue
Li, Caili
Zhang, Chen
Lin, Hai
Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
title Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
title_full Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
title_fullStr Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
title_full_unstemmed Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
title_short Predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
title_sort predictive value of early molecular response for deep molecular response in chronic phase of chronic myeloid leukemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6485861/
https://www.ncbi.nlm.nih.gov/pubmed/30985724
http://dx.doi.org/10.1097/MD.0000000000015222
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