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A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors
Whether tyrosine kinase inhibitors (TKIs) can be safely discontinued is a key focus of chronic myelogenous leukemia (CML) at present. We report a clinical observation of TKIs cessation in Chinese CML patients and a probable connection between CML leukemia stem cells (LSCs) and relapse. In all, 22 of...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295427/ https://www.ncbi.nlm.nih.gov/pubmed/27533462 http://dx.doi.org/10.18632/oncotarget.11281 |
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author | Li, Qing Zhong, Zhaodong Zeng, Chen Meng, Li Li, Chunrui Luo, Yi Wang, Hongxiang Li, Weiming Wang, Jue Cheng, Fanjun Guo, Anyuan Liu, Songya Jin, Caibao Zhu, Xiaojian You, Yong Zou, Ping |
author_facet | Li, Qing Zhong, Zhaodong Zeng, Chen Meng, Li Li, Chunrui Luo, Yi Wang, Hongxiang Li, Weiming Wang, Jue Cheng, Fanjun Guo, Anyuan Liu, Songya Jin, Caibao Zhu, Xiaojian You, Yong Zou, Ping |
author_sort | Li, Qing |
collection | PubMed |
description | Whether tyrosine kinase inhibitors (TKIs) can be safely discontinued is a key focus of chronic myelogenous leukemia (CML) at present. We report a clinical observation of TKIs cessation in Chinese CML patients and a probable connection between CML leukemia stem cells (LSCs) and relapse. In all, 22 of 1057 patients consented to participate in this observation. The average time of complete molecular response was 12.73 months after TKI withdrawal. LSCs could be flow cytometrically detected in most of the patients. However, the number of LSCs did not differ between the relapsers and non-relapsers. We evaluated the leukemogenetic ability of the LSCs by transplanting bone marrow into irradiated NOD/SCID mice. The results indicated that part of the bone marrow from the relapsers lead to leukemogensis in the mice. Besides, we found that LSCs-derived microvesicles might serve as a novel factor for the stratification of undetectable minimal residual disease and an early warning sign of relapse. In summary, post-TKI cessation relapse seems to show none association with the number of LSCs. A mouse xenograft model would provide a novel and useful method of analyzing LSCs function and predicting relapse. Microvesicles may provide important information about optimal molecular monitoring schedules in TKI discontinuation strategies. |
format | Online Article Text |
id | pubmed-5295427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52954272017-02-08 A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors Li, Qing Zhong, Zhaodong Zeng, Chen Meng, Li Li, Chunrui Luo, Yi Wang, Hongxiang Li, Weiming Wang, Jue Cheng, Fanjun Guo, Anyuan Liu, Songya Jin, Caibao Zhu, Xiaojian You, Yong Zou, Ping Oncotarget Research Paper Whether tyrosine kinase inhibitors (TKIs) can be safely discontinued is a key focus of chronic myelogenous leukemia (CML) at present. We report a clinical observation of TKIs cessation in Chinese CML patients and a probable connection between CML leukemia stem cells (LSCs) and relapse. In all, 22 of 1057 patients consented to participate in this observation. The average time of complete molecular response was 12.73 months after TKI withdrawal. LSCs could be flow cytometrically detected in most of the patients. However, the number of LSCs did not differ between the relapsers and non-relapsers. We evaluated the leukemogenetic ability of the LSCs by transplanting bone marrow into irradiated NOD/SCID mice. The results indicated that part of the bone marrow from the relapsers lead to leukemogensis in the mice. Besides, we found that LSCs-derived microvesicles might serve as a novel factor for the stratification of undetectable minimal residual disease and an early warning sign of relapse. In summary, post-TKI cessation relapse seems to show none association with the number of LSCs. A mouse xenograft model would provide a novel and useful method of analyzing LSCs function and predicting relapse. Microvesicles may provide important information about optimal molecular monitoring schedules in TKI discontinuation strategies. Impact Journals LLC 2016-08-13 /pmc/articles/PMC5295427/ /pubmed/27533462 http://dx.doi.org/10.18632/oncotarget.11281 Text en Copyright: © 2016 Li et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Li, Qing Zhong, Zhaodong Zeng, Chen Meng, Li Li, Chunrui Luo, Yi Wang, Hongxiang Li, Weiming Wang, Jue Cheng, Fanjun Guo, Anyuan Liu, Songya Jin, Caibao Zhu, Xiaojian You, Yong Zou, Ping A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
title | A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
title_full | A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
title_fullStr | A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
title_full_unstemmed | A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
title_short | A clinical observation of Chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
title_sort | clinical observation of chinese chronic myelogenous leukemia patients after discontinuation of tyrosine kinase inhibitors |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5295427/ https://www.ncbi.nlm.nih.gov/pubmed/27533462 http://dx.doi.org/10.18632/oncotarget.11281 |
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