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Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia

The treatment of Ph-positive acute lymphoblastic leukemia (Ph+ ALL) has entranced tyrosine kinase inhibitors (TKIs) era. Currently both imatinib and dasatinib are registered as the front-line treatment for Ph+ ALL, and the other 2(nd)-generation TKIs are suggested as an alternative for those who fai...

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Autores principales: Yu, Guopan, Chen, Fang, Yin, Changxin, Liu, Qifa, Sun, Jing, Xuan, Li, Fan, Zhiping, Wang, Qiang, Liu, Xiaoli, Jiang, Qianli, Xu, Dan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739793/
https://www.ncbi.nlm.nih.gov/pubmed/29291008
http://dx.doi.org/10.18632/oncotarget.22206
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author Yu, Guopan
Chen, Fang
Yin, Changxin
Liu, Qifa
Sun, Jing
Xuan, Li
Fan, Zhiping
Wang, Qiang
Liu, Xiaoli
Jiang, Qianli
Xu, Dan
author_facet Yu, Guopan
Chen, Fang
Yin, Changxin
Liu, Qifa
Sun, Jing
Xuan, Li
Fan, Zhiping
Wang, Qiang
Liu, Xiaoli
Jiang, Qianli
Xu, Dan
author_sort Yu, Guopan
collection PubMed
description The treatment of Ph-positive acute lymphoblastic leukemia (Ph+ ALL) has entranced tyrosine kinase inhibitors (TKIs) era. Currently both imatinib and dasatinib are registered as the front-line treatment for Ph+ ALL, and the other 2(nd)-generation TKIs are suggested as an alternative for those who failed the first-line treatment. However, it remains unclear who could benefit from the 2(nd)-generation TKIs as the first-line treatment for Ph+ ALL. In this study we compared the efficacy and safety of the 1(st) and 2(nd)-generation TKIs in the front-line treatment of Ph+ ALL and found a trend toward better disease-free survival (DFS) in the 2(nd)-generation TKIs group, though no significant difference in early response and long-term survival between the two groups. Furthermore, subgroup analysis showed that if allogeneic hematopoietic stem cell transplantation (allo-HSCT) was incorporated as consolidation, the 2(nd)-generation TKIs benefited patients with better DFS and overall survival (OS). The two generation TKIs were well tolerated. Higher incidence of acquiring T315I mutation was observed in the patients relapsed on the 2(nd)-generation TKIs. These findings suggested front-line treatment of Ph+ ALL with the 2(nd)-generation TKIs might benefit patients with better survival when allo-HSCT was incorporated as consolidation therapy; meanwhile, the higher incidence of T315I mutation in patients relapsed on the 2(nd)-generation TKIs deserved further attention.
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spelling pubmed-57397932017-12-29 Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia Yu, Guopan Chen, Fang Yin, Changxin Liu, Qifa Sun, Jing Xuan, Li Fan, Zhiping Wang, Qiang Liu, Xiaoli Jiang, Qianli Xu, Dan Oncotarget Research Paper The treatment of Ph-positive acute lymphoblastic leukemia (Ph+ ALL) has entranced tyrosine kinase inhibitors (TKIs) era. Currently both imatinib and dasatinib are registered as the front-line treatment for Ph+ ALL, and the other 2(nd)-generation TKIs are suggested as an alternative for those who failed the first-line treatment. However, it remains unclear who could benefit from the 2(nd)-generation TKIs as the first-line treatment for Ph+ ALL. In this study we compared the efficacy and safety of the 1(st) and 2(nd)-generation TKIs in the front-line treatment of Ph+ ALL and found a trend toward better disease-free survival (DFS) in the 2(nd)-generation TKIs group, though no significant difference in early response and long-term survival between the two groups. Furthermore, subgroup analysis showed that if allogeneic hematopoietic stem cell transplantation (allo-HSCT) was incorporated as consolidation, the 2(nd)-generation TKIs benefited patients with better DFS and overall survival (OS). The two generation TKIs were well tolerated. Higher incidence of acquiring T315I mutation was observed in the patients relapsed on the 2(nd)-generation TKIs. These findings suggested front-line treatment of Ph+ ALL with the 2(nd)-generation TKIs might benefit patients with better survival when allo-HSCT was incorporated as consolidation therapy; meanwhile, the higher incidence of T315I mutation in patients relapsed on the 2(nd)-generation TKIs deserved further attention. Impact Journals LLC 2017-10-31 /pmc/articles/PMC5739793/ /pubmed/29291008 http://dx.doi.org/10.18632/oncotarget.22206 Text en Copyright: © 2017 Yu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Yu, Guopan
Chen, Fang
Yin, Changxin
Liu, Qifa
Sun, Jing
Xuan, Li
Fan, Zhiping
Wang, Qiang
Liu, Xiaoli
Jiang, Qianli
Xu, Dan
Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia
title Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia
title_full Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia
title_fullStr Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia
title_full_unstemmed Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia
title_short Upfront treatment with the first and second-generation tyrosine kinase inhibitors in Ph-positive acute lymphoblastic leukemia
title_sort upfront treatment with the first and second-generation tyrosine kinase inhibitors in ph-positive acute lymphoblastic leukemia
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5739793/
https://www.ncbi.nlm.nih.gov/pubmed/29291008
http://dx.doi.org/10.18632/oncotarget.22206
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