Cargando…

异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析

OBJECTIVE: To evaluate the outcomes and prognostic factors of myelodysplasia syndrome (MDS) patients who received allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: 165 cases of MDS who underwent allo-HSCT from Jan. 2010 to Mar. 2018 were analyzed retrospectively, focusing on t...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342395/
https://www.ncbi.nlm.nih.gov/pubmed/31340621
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.007
_version_ 1783555470799142912
collection PubMed
description OBJECTIVE: To evaluate the outcomes and prognostic factors of myelodysplasia syndrome (MDS) patients who received allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: 165 cases of MDS who underwent allo-HSCT from Jan. 2010 to Mar. 2018 were analyzed retrospectively, focusing on the overall survival (OS), disease free survival (DFS), relapse, non-relapse mortality (NRM) and their related risk factors. RESULTS: Of all the 165 cases, 105 were male and 60 were female. The 3-year OS and DFS rate were 72.5% (95%CI 64.9%–80.1%) and 67.4% (95%CI 59.17%–75.63%), respectively. The 3-year cumulative incidence of relapse and NRM were 12.11% (95%CI 7.03%–18.65%) and 20.44% (95%CI 14.15%–27.56%), respectively. HCT-comorbidity index (P=0.042, HR=2.094, 95%CI 1.026–4.274) was identified as independent risk factor for OS by the multivariate analysis. Intensive chemotherapy before HSCT or hypomethylation agents treatment had no effects on OS[ (67.0±7.5) %vs (57.7±10.9) %, χ(2)=0.025, P=0.874]. CONCLUSION: allo-HSCT is a promising means for MDS, and NRM is the major cause of treatment failure. MDS with refractory anemia with excess blasts and secondary acute myeloid leukemia patients may not benefit from intensive chemotherapy or hypomethylation agents treatment before HSCT.
format Online
Article
Text
id pubmed-7342395
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Editorial office of Chinese Journal of Hematology
record_format MEDLINE/PubMed
spelling pubmed-73423952020-07-16 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To evaluate the outcomes and prognostic factors of myelodysplasia syndrome (MDS) patients who received allogeneic hematopoietic stem cell transplantation (allo-HSCT). METHODS: 165 cases of MDS who underwent allo-HSCT from Jan. 2010 to Mar. 2018 were analyzed retrospectively, focusing on the overall survival (OS), disease free survival (DFS), relapse, non-relapse mortality (NRM) and their related risk factors. RESULTS: Of all the 165 cases, 105 were male and 60 were female. The 3-year OS and DFS rate were 72.5% (95%CI 64.9%–80.1%) and 67.4% (95%CI 59.17%–75.63%), respectively. The 3-year cumulative incidence of relapse and NRM were 12.11% (95%CI 7.03%–18.65%) and 20.44% (95%CI 14.15%–27.56%), respectively. HCT-comorbidity index (P=0.042, HR=2.094, 95%CI 1.026–4.274) was identified as independent risk factor for OS by the multivariate analysis. Intensive chemotherapy before HSCT or hypomethylation agents treatment had no effects on OS[ (67.0±7.5) %vs (57.7±10.9) %, χ(2)=0.025, P=0.874]. CONCLUSION: allo-HSCT is a promising means for MDS, and NRM is the major cause of treatment failure. MDS with refractory anemia with excess blasts and secondary acute myeloid leukemia patients may not benefit from intensive chemotherapy or hypomethylation agents treatment before HSCT. Editorial office of Chinese Journal of Hematology 2019-06 /pmc/articles/PMC7342395/ /pubmed/31340621 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.007 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
异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
title 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
title_full 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
title_fullStr 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
title_full_unstemmed 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
title_short 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
title_sort 异基因造血干细胞移植治疗骨髓增生异常综合征的预后因素分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7342395/
https://www.ncbi.nlm.nih.gov/pubmed/31340621
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2019.06.007
work_keys_str_mv AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī
AT yìjīyīnzàoxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēngdeyùhòuyīnsùfēnxī