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骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义
OBJECTIVE: To monitor the WT1 mRNA level and its dynamic changes in patients with myelodysplastic syndromes (MDS) after hypomethylating agents (HMA), as well as to assess the significance of WT1 mRNA levels and its dynamic changes in evaluating the efficacy of HMA and distinguishing the disease stat...
Formato: | Online Artículo Texto |
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Lenguaje: | English |
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Editorial office of Chinese Journal of Hematology
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342245/ https://www.ncbi.nlm.nih.gov/pubmed/31207708 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.05.013 |
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collection | PubMed |
description | OBJECTIVE: To monitor the WT1 mRNA level and its dynamic changes in patients with myelodysplastic syndromes (MDS) after hypomethylating agents (HMA), as well as to assess the significance of WT1 mRNA levels and its dynamic changes in evaluating the efficacy of HMA and distinguishing the disease status of heterogeneous patients with stable disease (SD). METHODS: Bone marrow or peripheral blood samples of 56 patients with MDS who underwent hypomethylating agents (≥4 cycles) from November 2009 to March 2018 were tested by real-time quantitative polymerase chain reaction (PCR) to detect the expression of WT1 mRNA, and to observe the correlation between the dynamic changes of WT1 mRNA expression and clinical efficacy and prognosis of patients. RESULTS: WT1 mRNA expression levels of MDS patients decreased significantly after 3 cycles of hypomethylating agent treatment. Besides, the WT1 mRNA expression levels of patients increased significantly after diseases progression. According to the dynamic changes of WT1 mRNA expression levels during SD, 45 cases could be further divided into increased group and non-increased group. In those SD patients with increased WT1 mRNA expression level, the ratio of suffering disease progression or transformation to AML was 95.65% (22/23), whereas the ratio turned to be 9.09% (2/22) for the non-increased group (χ(2)=33.852, P<0.001). Compared with those SD patients reporting no increase in WT1 mRNA expression level, the overall survival [17 (95%CI 11–23) months vs not reached, P<0.001] and progression-free survival [13 (95%CI 8–18) months vs not reached, P<0.001] of those SD patients reporting increase in WT1 mRNA expression level were significantly shorter. CONCLUSION: WT1 mRNA expression level is a useful indicator to assess the efficacy of hypomethylating agents in MDS patients. Especially in patients with SD, detection of the changes in WT1 mRNA expression level is able to predict disease progression and help to make clinical decision. |
format | Online Article Text |
id | pubmed-7342245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Editorial office of Chinese Journal of Hematology |
record_format | MEDLINE/PubMed |
spelling | pubmed-73422452020-07-16 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To monitor the WT1 mRNA level and its dynamic changes in patients with myelodysplastic syndromes (MDS) after hypomethylating agents (HMA), as well as to assess the significance of WT1 mRNA levels and its dynamic changes in evaluating the efficacy of HMA and distinguishing the disease status of heterogeneous patients with stable disease (SD). METHODS: Bone marrow or peripheral blood samples of 56 patients with MDS who underwent hypomethylating agents (≥4 cycles) from November 2009 to March 2018 were tested by real-time quantitative polymerase chain reaction (PCR) to detect the expression of WT1 mRNA, and to observe the correlation between the dynamic changes of WT1 mRNA expression and clinical efficacy and prognosis of patients. RESULTS: WT1 mRNA expression levels of MDS patients decreased significantly after 3 cycles of hypomethylating agent treatment. Besides, the WT1 mRNA expression levels of patients increased significantly after diseases progression. According to the dynamic changes of WT1 mRNA expression levels during SD, 45 cases could be further divided into increased group and non-increased group. In those SD patients with increased WT1 mRNA expression level, the ratio of suffering disease progression or transformation to AML was 95.65% (22/23), whereas the ratio turned to be 9.09% (2/22) for the non-increased group (χ(2)=33.852, P<0.001). Compared with those SD patients reporting no increase in WT1 mRNA expression level, the overall survival [17 (95%CI 11–23) months vs not reached, P<0.001] and progression-free survival [13 (95%CI 8–18) months vs not reached, P<0.001] of those SD patients reporting increase in WT1 mRNA expression level were significantly shorter. CONCLUSION: WT1 mRNA expression level is a useful indicator to assess the efficacy of hypomethylating agents in MDS patients. Especially in patients with SD, detection of the changes in WT1 mRNA expression level is able to predict disease progression and help to make clinical decision. Editorial office of Chinese Journal of Hematology 2019-05 /pmc/articles/PMC7342245/ /pubmed/31207708 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.05.013 Text en 2019年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal. |
spellingShingle | 论著 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 |
title | 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 |
title_full | 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 |
title_fullStr | 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 |
title_full_unstemmed | 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 |
title_short | 骨髓增生异常综合征患者去甲基化治疗后WT1 mRNA水平的变化及其预后意义 |
title_sort | 骨髓增生异常综合征患者去甲基化治疗后wt1 mrna水平的变化及其预后意义 |
topic | 论著 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342245/ https://www.ncbi.nlm.nih.gov/pubmed/31207708 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.05.013 |
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