Cargando…

HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析

OBJECTIVE: To evaluate the outcomes of myelodysplastic syndromes (MDS) patients who received HLA-matched sibling donor allogeneic peripheral blood stem cell transplantation (MSD-PBSCT). METHODS: The clinical data of 138 MDS patients received MSD-PBSCT from Sep. 2005 to Dec. 2017 were retrospectively...

Descripción completa

Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357951/
https://www.ncbi.nlm.nih.gov/pubmed/32135630
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.02.009
_version_ 1783558768597925888
collection PubMed
description OBJECTIVE: To evaluate the outcomes of myelodysplastic syndromes (MDS) patients who received HLA-matched sibling donor allogeneic peripheral blood stem cell transplantation (MSD-PBSCT). METHODS: The clinical data of 138 MDS patients received MSD-PBSCT from Sep. 2005 to Dec. 2017 were retrospectively analyzed, and the overall survival (OS) rate, disease-free survival (DFS) rate, relapse rate (RR), non-relapse mortality (NRM) rate and the related risk factors were explored. RESULTS: ①After a median follow-up of 1 050 (range 4 to 4 988) days, the 3-year OS and DFS rates were (66.6±4.1) % and (63.3±4.1) %, respectively. The 3-year cumulative incidence of RR and NRM rates were (13.9±0.1) % and (22.2±0.1) %, respectively. ②Univariate analysis showed that patients with grade Ⅲ–Ⅳ acute graft-versus-host disease (aGVHD) or hematopoietic cell transplantation comorbidity index (HCT-CI) ≥2 points or patients in very high-risk group of the Revised International Prognostic Scoring System (IPSS-R) had significantly decreased OS [(42.9±13.2) %vs (72.9±4.2) %, χ(2)=8.620, P=0.003; (53.3±7.6) %vs (72.6±4.7) %, χ(2)=6.681, P=0.010; (53.8±6.8) %vs (76.6±6.2) %vs (73.3±7.7) %, χ(2)=6.337, P=0.042]. For MDS patients with excess blasts-2 (MDS-EB2) and acute myeloid leukemia patients derived from MDS (MDS-AML), pre-transplant chemotherapy or hypomethylating agents (HMA) therapy could not improve the OS rate [(60.4±7.8) %vs (59.2±9.6) %, χ(2)=0.042, P=0.838]. ③Multivariate analysis indicated that the HCT-CI was an independent risk factor for OS and DFS (P=0.012, HR=2.108, 95%CI 1.174–3.785; P=0.008, HR=2.128, 95%CI 1.219–3.712). CONCLUSIONS: HCT-CI was better than the IPSS-R in predicting the outcomes after transplantation. The occurrence of grade Ⅲ–Ⅳ aGVHD is a poor prognostic factor for OS. For patients of MDS-EB2 and MDS-AML, immediate transplantation was recommended instead of receiving pre-transplant chemotherapy or HMA therapy.
format Online
Article
Text
id pubmed-7357951
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Editorial office of Chinese Journal of Hematology
record_format MEDLINE/PubMed
spelling pubmed-73579512020-07-16 HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: To evaluate the outcomes of myelodysplastic syndromes (MDS) patients who received HLA-matched sibling donor allogeneic peripheral blood stem cell transplantation (MSD-PBSCT). METHODS: The clinical data of 138 MDS patients received MSD-PBSCT from Sep. 2005 to Dec. 2017 were retrospectively analyzed, and the overall survival (OS) rate, disease-free survival (DFS) rate, relapse rate (RR), non-relapse mortality (NRM) rate and the related risk factors were explored. RESULTS: ①After a median follow-up of 1 050 (range 4 to 4 988) days, the 3-year OS and DFS rates were (66.6±4.1) % and (63.3±4.1) %, respectively. The 3-year cumulative incidence of RR and NRM rates were (13.9±0.1) % and (22.2±0.1) %, respectively. ②Univariate analysis showed that patients with grade Ⅲ–Ⅳ acute graft-versus-host disease (aGVHD) or hematopoietic cell transplantation comorbidity index (HCT-CI) ≥2 points or patients in very high-risk group of the Revised International Prognostic Scoring System (IPSS-R) had significantly decreased OS [(42.9±13.2) %vs (72.9±4.2) %, χ(2)=8.620, P=0.003; (53.3±7.6) %vs (72.6±4.7) %, χ(2)=6.681, P=0.010; (53.8±6.8) %vs (76.6±6.2) %vs (73.3±7.7) %, χ(2)=6.337, P=0.042]. For MDS patients with excess blasts-2 (MDS-EB2) and acute myeloid leukemia patients derived from MDS (MDS-AML), pre-transplant chemotherapy or hypomethylating agents (HMA) therapy could not improve the OS rate [(60.4±7.8) %vs (59.2±9.6) %, χ(2)=0.042, P=0.838]. ③Multivariate analysis indicated that the HCT-CI was an independent risk factor for OS and DFS (P=0.012, HR=2.108, 95%CI 1.174–3.785; P=0.008, HR=2.128, 95%CI 1.219–3.712). CONCLUSIONS: HCT-CI was better than the IPSS-R in predicting the outcomes after transplantation. The occurrence of grade Ⅲ–Ⅳ aGVHD is a poor prognostic factor for OS. For patients of MDS-EB2 and MDS-AML, immediate transplantation was recommended instead of receiving pre-transplant chemotherapy or HMA therapy. Editorial office of Chinese Journal of Hematology 2020-02 /pmc/articles/PMC7357951/ /pubmed/32135630 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.02.009 Text en 2020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
HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
title HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
title_full HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
title_fullStr HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
title_full_unstemmed HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
title_short HLA匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
title_sort hla匹配同胞供者异基因外周血干细胞移植治疗骨髓增生异常综合征138例疗效分析
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357951/
https://www.ncbi.nlm.nih.gov/pubmed/32135630
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.02.009
work_keys_str_mv AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī
AT hlapǐpèitóngbāogōngzhěyìjīyīnwàizhōuxuègànxìbāoyízhízhìliáogǔsuǐzēngshēngyìchángzōnghézhēng138lìliáoxiàofēnxī