Intensified conditioning containing decitabine versus standard myeloablative conditioning for adult patients with KMT2A-rearranged leukemia: a multicenter retrospective study

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablati...

Full description

Saved in:
Bibliographic Details
Published inBMC medicine Vol. 22; no. 1; pp. 605 - 11
Main Authors Hu, Zhongli, Feng, Zinan, Liu, Shiqi, He, Hai, Dong, Ying, Fan, Zhiping, Li, Yiqing, Huang, Fen, Xu, Na, Liu, Can, Zeng, Yunxin, Zhu, Ping, Lin, Ren, Jin, Hua, Zhang, Xiong, Sun, Ruijuan, Liu, Qifa, Xuan, Li
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 31.12.2024
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia. We performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m /day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m /day on days -10 to -6; the same dose of TBI-Cy). Between April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups. These results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.
AbstractList Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia. Methods We performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m.sup.2/day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m.sup.2/day on days -10 to -6; the same dose of TBI-Cy). Results Between April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups. Conclusions These results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT. Keywords: Decitabine, Intensified conditioning, Allo-HSCT, KMT2A-r leukemia
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia. We performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m /day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m /day on days -10 to -6; the same dose of TBI-Cy). Between April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups. These results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.
Abstract Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia. Methods We performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m2/day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m2/day on days -10 to -6; the same dose of TBI-Cy). Results Between April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups. Conclusions These results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia.BACKGROUNDAllogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia.We performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m2/day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m2/day on days -10 to -6; the same dose of TBI-Cy).METHODSWe performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m2/day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m2/day on days -10 to -6; the same dose of TBI-Cy).Between April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups.RESULTSBetween April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups.These results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.CONCLUSIONSThese results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.
BackgroundAllogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia.MethodsWe performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m2/day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m2/day on days -10 to -6; the same dose of TBI-Cy).ResultsBetween April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups.ConclusionsThese results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains high. We aimed to determine whether intensified conditioning containing decitabine (Dec) could reduce relapse compared with standard myeloablative conditioning in adult patients with KMT2A-r leukemia. We performed a multicenter retrospective study at seven institutions in China. Eligible patients were aged 14 years or older at transplantation, had a diagnosis of KMT2A-r leukemia, and underwent the first allo-HSCT. Standard myeloablative conditioning regimens (standard group) included BuCy (busulfan 3.2 mg/kg/day on days -7 to -4; cyclophosphamide 60 mg/kg/day on days -3 to -2) and TBI-Cy (total body irradiation 4.5 Gy/day on days -5 to -4; Cy 60 mg/kg/day on days -3 to -2). Intensified conditioning regimens containing Dec (intensified group) consisted of Dec-BuCy (Dec 20 mg/m.sup.2/day on days -14 to -10; the same dose of BuCy) and Dec-TBI-Cy (Dec 20 mg/m.sup.2/day on days -10 to -6; the same dose of TBI-Cy). Between April 2009 and December 2019, 218 patients were included in this study, of whom 105 were in the intensified group and 113 were in the standard group. The 3-year cumulative incidence of relapse was 17.6% and 34.5%, overall survival was 71.3% and 61.0%, disease-free survival was 70.1% and 56.0%, and non-relapse mortality was 12.3% and 9.5% in the intensified and standard groups, respectively (P = 0.001; P = 0.034; P = 0.005; P = 0.629). Subgroup analysis showed that the relapse rate of intensified conditioning was lower than that of standard conditioning in multiple subgroups, including different leukemia types, disease status at transplantation, high-risk cytogenetics and Bu-based regimens. There was no difference in regimen-related toxicity, engraftment, or graft-versus-host disease between the intensified and standard groups. These results suggest that intensified conditioning containing Dec might be a better strategy than standard myeloablative conditioning for adult patients with KMT2A-r leukemia undergoing allo-HSCT.
ArticleNumber 605
Audience Academic
Author Huang, Fen
Li, Yiqing
Zeng, Yunxin
Jin, Hua
He, Hai
Xu, Na
Sun, Ruijuan
Zhu, Ping
Liu, Can
Lin, Ren
Fan, Zhiping
Hu, Zhongli
Dong, Ying
Xuan, Li
Feng, Zinan
Liu, Shiqi
Liu, Qifa
Zhang, Xiong
Author_xml – sequence: 1
  givenname: Zhongli
  surname: Hu
  fullname: Hu, Zhongli
– sequence: 2
  givenname: Zinan
  surname: Feng
  fullname: Feng, Zinan
– sequence: 3
  givenname: Shiqi
  surname: Liu
  fullname: Liu, Shiqi
– sequence: 4
  givenname: Hai
  surname: He
  fullname: He, Hai
– sequence: 5
  givenname: Ying
  surname: Dong
  fullname: Dong, Ying
– sequence: 6
  givenname: Zhiping
  surname: Fan
  fullname: Fan, Zhiping
– sequence: 7
  givenname: Yiqing
  surname: Li
  fullname: Li, Yiqing
– sequence: 8
  givenname: Fen
  surname: Huang
  fullname: Huang, Fen
– sequence: 9
  givenname: Na
  surname: Xu
  fullname: Xu, Na
– sequence: 10
  givenname: Can
  surname: Liu
  fullname: Liu, Can
– sequence: 11
  givenname: Yunxin
  surname: Zeng
  fullname: Zeng, Yunxin
– sequence: 12
  givenname: Ping
  surname: Zhu
  fullname: Zhu, Ping
– sequence: 13
  givenname: Ren
  surname: Lin
  fullname: Lin, Ren
– sequence: 14
  givenname: Hua
  surname: Jin
  fullname: Jin, Hua
– sequence: 15
  givenname: Xiong
  surname: Zhang
  fullname: Zhang, Xiong
– sequence: 16
  givenname: Ruijuan
  surname: Sun
  fullname: Sun, Ruijuan
– sequence: 17
  givenname: Qifa
  surname: Liu
  fullname: Liu, Qifa
– sequence: 18
  givenname: Li
  surname: Xuan
  fullname: Xuan, Li
BackLink https://www.ncbi.nlm.nih.gov/pubmed/39736728$$D View this record in MEDLINE/PubMed
BookMark eNptktuO0zAQhiO0iD3AC3CBIiEhbrLYjuO43KyqFYeKRdws19bEnrReUrvYTlFfimfEbZeqRciSj5__8Yz_y-LMeYdF8ZKSa0qleBcpm1BREcYrUsuaVORJcUFbTquW0ObsaH5eXMb4QAhr2pY_K87rSVuLlsmL4vfMJXTR9hZNqb0zNlnvrJtvFwnsbmpQ2wSddViuMcQxljGBMxBMudzg4KEbINk1ngr0PpRgxiGVq3yKLsXyl02L8svXezatAkII4OY57IDjD1xaeF9Cucy81RnGUAZMwccV6p12TKPZPC-e9jBEfPE4XhXfP364v_1c3X37NLud3lW64SJVvGOCcQAKnQEjmO641BSNyQOjWmvTsRo6IppGcylBT0zTMEmE7JFAjfVVMdvrGg8PahXsEsJGebBqt-HDXEHIDx1Q9R0VGlrR5ECckaYjugOY1FLnUIKyrHWz11qN3RLNNrkAw4no6YmzCzX3a0WpkC3hIiu8fVQI_ueIMamljRqHARz6MaqaNqTmOQGe0df_oA9-DC7XaksxMWl5Zg_UHHIG1vU-B9ZbUTWVjErZTGSdqev_ULmZ_Fv5q7G3ef_kwpujCwuEIS2iH8atI-Ip-Oq4JIda_PVlBtge0NkBMWB_QChRW_OrvflVNr_amT_3fwDCE_rB
Cites_doi 10.1038/s41408-021-00557-6
10.1016/j.canlet.2024.217264
10.1182/blood.2022017645
10.6004/jnccn.2023.0025
10.1016/j.bbmt.2014.12.001
10.1200/JCO.2008.16.7981
10.1038/s41375-021-01218-0
10.1038/s41375-021-01135-2
10.1002/sim.7501
10.3389/fonc.2022.844937
10.1038/s41409-021-01238-5
10.6004/jnccn.2021.0042
10.1002/(SICI)1097-0258(19990330)18:6<695::AID-SIM60>3.0.CO;2-O
10.1038/s41375-023-01877-1
10.1200/JCO.1988.6.10.1562
10.1016/j.bbmt.2018.07.021
10.6004/jnccn.2020.0021
10.1016/j.exphem.2018.08.002
10.1200/JCO.22.01297
10.1200/JCO.19.03011
10.1016/S2352-3026(23)00117-5
10.1002/(SICI)1096-8652(199806)58:2<130::AID-AJH8>3.0.CO;2-T
10.12659/MSM.899186
10.1038/leu.2015.143
10.1038/s41409-020-0803-y
10.1186/s13045-020-00859-5
10.1158/1078-0432.CCR-06-2762
10.1038/s41591-022-01720-7
10.2147/CMAR.S229768
10.1038/s41586-023-05812-3
10.1126/scitranslmed.abc4834
10.1016/S2352-3026(22)00375-1
10.1186/s13045-021-01159-2
10.1182/blood-2009-04-215152
10.1200/JCO.22.02120
10.1186/s13045-021-01057-7
10.1016/j.blre.2016.08.005
10.1038/s43018-022-00366-1
10.1056/NEJMoa2004444
ContentType Journal Article
Copyright 2024. The Author(s).
COPYRIGHT 2024 BioMed Central Ltd.
2024. This work is licensed under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
The Author(s) 2024 2024
Copyright_xml – notice: 2024. The Author(s).
– notice: COPYRIGHT 2024 BioMed Central Ltd.
– notice: 2024. This work is licensed under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: The Author(s) 2024 2024
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7QL
7U9
7X7
7XB
88E
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
C1K
CCPQU
DWQXO
FYUFA
GHDGH
H94
K9.
M0S
M1P
M7N
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1186/s12916-024-03830-0
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Bacteriology Abstracts (Microbiology B)
Virology and AIDS Abstracts
ProQuest Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
Environmental Sciences and Pollution Management
ProQuest One
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Health & Medical Collection (Alumni)
Medical Database
Algology Mycology and Protozoology Abstracts (Microbiology C)
ProQuest Central Premium
ProQuest One Academic
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central China
Environmental Sciences and Pollution Management
ProQuest Central
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Bacteriology Abstracts (Microbiology B)
Algology Mycology and Protozoology Abstracts (Microbiology C)
Health & Medical Research Collection
AIDS and Cancer Research Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
Virology and AIDS Abstracts
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList

MEDLINE

MEDLINE - Academic
Publicly Available Content Database

Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1741-7015
EndPage 11
ExternalDocumentID oai_doaj_org_article_fb16ca765ad64205b0cbaa938cc21612
PMC11687046
A821885983
39736728
10_1186_s12916_024_03830_0
Genre Multicenter Study
Comparative Study
Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations China
GeographicLocations_xml – name: China
GrantInformation_xml – fundername: National Natural Science Foundation of China
  grantid: 82293634
– fundername: National Key Research and Development Program of China
  grantid: 2021YFC2500300-4
– fundername: National Key Research and Development Program of China
  grantid: 2022YFC2502600-5
– fundername: Natural Science Foundation of Guangdong Province
  grantid: 2024A1515010794
– fundername: National Natural Science Foundation of China
  grantid: 82170213
GroupedDBID ---
0R~
23N
2WC
4.4
53G
5GY
5VS
6J9
6PF
7X7
88E
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAWTL
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AENEX
AFKRA
AFPKN
AFRAH
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
DU5
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
IHW
INH
INR
ITC
KQ8
M1P
M48
MK0
M~E
O5R
O5S
OK1
OVT
P2P
PGMZT
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SMD
SOJ
SV3
TR2
TUS
UKHRP
WOQ
WOW
XSB
CGR
CUY
CVF
ECM
EIF
NPM
PJZUB
PPXIY
PUEGO
PMFND
3V.
7QL
7U9
7XB
8FK
AZQEC
C1K
DWQXO
H94
K9.
M7N
PKEHL
PQEST
PQUKI
PRINS
7X8
5PM
ID FETCH-LOGICAL-c546t-4b2624aa1abdad62cb48c1edd48c21cccdb23ab0655c488ac9d5528068fe0a3e3
IEDL.DBID M48
ISSN 1741-7015
IngestDate Wed Aug 27 01:18:58 EDT 2025
Thu Aug 21 18:35:44 EDT 2025
Fri Jul 11 10:58:26 EDT 2025
Fri Jul 25 21:48:41 EDT 2025
Tue Jun 17 21:59:12 EDT 2025
Tue Jun 10 20:58:39 EDT 2025
Thu May 22 21:23:36 EDT 2025
Thu Aug 28 04:45:46 EDT 2025
Tue Jul 01 02:51:43 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Decitabine
Intensified conditioning
Allo-HSCT
KMT2A-r leukemia
Language English
License 2024. The Author(s).
Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c546t-4b2624aa1abdad62cb48c1edd48c21cccdb23ab0655c488ac9d5528068fe0a3e3
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://www.proquest.com/docview/3152697450?pq-origsite=%requestingapplication%
PMID 39736728
PQID 3152697450
PQPubID 42775
PageCount 11
ParticipantIDs doaj_primary_oai_doaj_org_article_fb16ca765ad64205b0cbaa938cc21612
pubmedcentral_primary_oai_pubmedcentral_nih_gov_11687046
proquest_miscellaneous_3150345284
proquest_journals_3152697450
gale_infotracmisc_A821885983
gale_infotracacademiconefile_A821885983
gale_healthsolutions_A821885983
pubmed_primary_39736728
crossref_primary_10_1186_s12916_024_03830_0
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-12-31
PublicationDateYYYYMMDD 2024-12-31
PublicationDate_xml – month: 12
  year: 2024
  text: 2024-12-31
  day: 31
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle BMC medicine
PublicationTitleAlternate BMC Med
PublicationYear 2024
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References J Krauter (3830_CR42) 2009; 27
X Tang (3830_CR16) 2021; 56
GC Issa (3830_CR6) 2021; 11
A Spyridonidis (3830_CR15) 2020; 55
L Xuan (3830_CR23) 2023; 10
DA Pollyea (3830_CR27) 2023; 21
R Zhang (3830_CR40) 2019; 25
BC Valdez (3830_CR37) 2018; 67
3830_CR24
C Meyer (3830_CR29) 2023; 37
HZ Qi (3830_CR11) 2021; 11
PC Austin (3830_CR34) 2017; 36
PA Brown (3830_CR28) 2021; 19
I Iacobucci (3830_CR8) 2022; 140
QY Wang (3830_CR22) 2019; 11
Y Wang (3830_CR10) 2014; 89
S Yu (3830_CR17) 2020; 13
H Zhang (3830_CR25) 2023; 41
BJ Aubrey (3830_CR7) 2022; 3
E Khabirova (3830_CR2) 2022; 28
AH Wei (3830_CR39) 2020; 383
GC Issa (3830_CR1) 2023; 615
3830_CR12
XH Zhang (3830_CR18) 2021; 14
3830_CR30
A Attarbaschi (3830_CR4) 2023; 41
3830_CR31
Y Wang (3830_CR19) 2024; 2024
L Xuan (3830_CR26) 2023; 10
BV Balgobind (3830_CR41) 2009; 114
TA Gooley (3830_CR33) 1999; 18
X Li (3830_CR5) 2021; 14
SI Bearman (3830_CR32) 1988; 6
H Yang (3830_CR9) 2016; 22
T Qin (3830_CR38) 2007; 13
RE van Weelderen (3830_CR3) 2023; 41
CS Hourigan (3830_CR14) 2020; 38
J Prada-Arismendy (3830_CR36) 2017; 31
J Stomper (3830_CR20) 2021; 35
Z Li (3830_CR21) 2022; 12
A Touzart (3830_CR35) 2021; 13
A Pigneux (3830_CR13) 2015; 29
References_xml – volume: 11
  start-page: 162
  issue: 9
  year: 2021
  ident: 3830_CR6
  publication-title: Blood Cancer J
  doi: 10.1038/s41408-021-00557-6
– volume: 11
  start-page: 1683
  issue: 4
  year: 2021
  ident: 3830_CR11
  publication-title: Am J Cancer Res
– volume: 2024
  start-page: 217264
  year: 2024
  ident: 3830_CR19
  publication-title: Cancer Lett
  doi: 10.1016/j.canlet.2024.217264
– volume: 140
  start-page: 1833
  issue: 17
  year: 2022
  ident: 3830_CR8
  publication-title: Blood
  doi: 10.1182/blood.2022017645
– volume: 21
  start-page: 503
  issue: 5
  year: 2023
  ident: 3830_CR27
  publication-title: J Natl Compr Canc Netw.
  doi: 10.6004/jnccn.2023.0025
– ident: 3830_CR31
  doi: 10.1016/j.bbmt.2014.12.001
– volume: 41
  start-page: 343
  issue: 2
  year: 2023
  ident: 3830_CR25
  publication-title: Phase III Trial J Clin Oncol
– volume: 27
  start-page: 3000
  issue: 18
  year: 2009
  ident: 3830_CR42
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.2008.16.7981
– volume: 35
  start-page: 1873
  issue: 7
  year: 2021
  ident: 3830_CR20
  publication-title: Leukemia
  doi: 10.1038/s41375-021-01218-0
– ident: 3830_CR12
  doi: 10.1038/s41375-021-01135-2
– volume: 36
  start-page: 4391
  issue: 27
  year: 2017
  ident: 3830_CR34
  publication-title: Stat Med
  doi: 10.1002/sim.7501
– volume: 12
  start-page: 844937
  year: 2022
  ident: 3830_CR21
  publication-title: Front Oncol
  doi: 10.3389/fonc.2022.844937
– volume: 56
  start-page: 1674
  issue: 7
  year: 2021
  ident: 3830_CR16
  publication-title: Bone Marrow Transplant
  doi: 10.1038/s41409-021-01238-5
– volume: 19
  start-page: 1079
  issue: 9
  year: 2021
  ident: 3830_CR28
  publication-title: J Natl Compr Canc Netw.
  doi: 10.6004/jnccn.2021.0042
– volume: 18
  start-page: 695
  issue: 6
  year: 1999
  ident: 3830_CR33
  publication-title: Stat Med
  doi: 10.1002/(SICI)1097-0258(19990330)18:6<695::AID-SIM60>3.0.CO;2-O
– volume: 37
  start-page: 988
  issue: 5
  year: 2023
  ident: 3830_CR29
  publication-title: Leukemia
  doi: 10.1038/s41375-023-01877-1
– volume: 6
  start-page: 1562
  issue: 10
  year: 1988
  ident: 3830_CR32
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.1988.6.10.1562
– volume: 25
  start-page: 47
  issue: 1
  year: 2019
  ident: 3830_CR40
  publication-title: Biol Blood Marrow Transplant
  doi: 10.1016/j.bbmt.2018.07.021
– ident: 3830_CR24
  doi: 10.6004/jnccn.2020.0021
– ident: 3830_CR30
– volume: 67
  start-page: 49
  year: 2018
  ident: 3830_CR37
  publication-title: Exp Hematol
  doi: 10.1016/j.exphem.2018.08.002
– volume: 41
  start-page: 1404
  issue: 7
  year: 2023
  ident: 3830_CR4
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.22.01297
– volume: 38
  start-page: 1273
  issue: 12
  year: 2020
  ident: 3830_CR14
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.19.03011
– volume: 10
  start-page: e600
  issue: 8
  year: 2023
  ident: 3830_CR26
  publication-title: Lancet Haematol
  doi: 10.1016/S2352-3026(23)00117-5
– volume: 89
  start-page: 130
  issue: 2
  year: 2014
  ident: 3830_CR10
  publication-title: Am J Hematol
  doi: 10.1002/(SICI)1096-8652(199806)58:2<130::AID-AJH8>3.0.CO;2-T
– volume: 22
  start-page: 2315
  year: 2016
  ident: 3830_CR9
  publication-title: Med Sci Monit
  doi: 10.12659/MSM.899186
– volume: 29
  start-page: 2375
  issue: 12
  year: 2015
  ident: 3830_CR13
  publication-title: Leukemia
  doi: 10.1038/leu.2015.143
– volume: 55
  start-page: 1114
  issue: 6
  year: 2020
  ident: 3830_CR15
  publication-title: Bone Marrow Transplant
  doi: 10.1038/s41409-020-0803-y
– volume: 13
  start-page: 18
  issue: 1
  year: 2020
  ident: 3830_CR17
  publication-title: J Hematol Oncol
  doi: 10.1186/s13045-020-00859-5
– volume: 13
  start-page: 4225
  issue: 14
  year: 2007
  ident: 3830_CR38
  publication-title: Clin Cancer Res
  doi: 10.1158/1078-0432.CCR-06-2762
– volume: 28
  start-page: 743
  issue: 4
  year: 2022
  ident: 3830_CR2
  publication-title: Nat Med
  doi: 10.1038/s41591-022-01720-7
– volume: 11
  start-page: 10195
  year: 2019
  ident: 3830_CR22
  publication-title: Cancer Manag Res
  doi: 10.2147/CMAR.S229768
– volume: 615
  start-page: 920
  issue: 7954
  year: 2023
  ident: 3830_CR1
  publication-title: Nature
  doi: 10.1038/s41586-023-05812-3
– volume: 13
  start-page: eabc4834
  issue: 595
  year: 2021
  ident: 3830_CR35
  publication-title: Sci Transl Med.
  doi: 10.1126/scitranslmed.abc4834
– volume: 10
  start-page: e178
  issue: 3
  year: 2023
  ident: 3830_CR23
  publication-title: Lancet Haematol
  doi: 10.1016/S2352-3026(22)00375-1
– volume: 14
  start-page: 145
  issue: 1
  year: 2021
  ident: 3830_CR18
  publication-title: J Hematol Oncol
  doi: 10.1186/s13045-021-01159-2
– volume: 114
  start-page: 2489
  issue: 12
  year: 2009
  ident: 3830_CR41
  publication-title: Blood
  doi: 10.1182/blood-2009-04-215152
– volume: 41
  start-page: 2963
  issue: 16
  year: 2023
  ident: 3830_CR3
  publication-title: J Clin Oncol
  doi: 10.1200/JCO.22.02120
– volume: 14
  start-page: 56
  issue: 1
  year: 2021
  ident: 3830_CR5
  publication-title: J Hematol Oncol
  doi: 10.1186/s13045-021-01057-7
– volume: 31
  start-page: 63
  issue: 1
  year: 2017
  ident: 3830_CR36
  publication-title: Blood Rev
  doi: 10.1016/j.blre.2016.08.005
– volume: 3
  start-page: 595
  issue: 5
  year: 2022
  ident: 3830_CR7
  publication-title: Nat Cancer
  doi: 10.1038/s43018-022-00366-1
– volume: 383
  start-page: 2526
  issue: 26
  year: 2020
  ident: 3830_CR39
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa2004444
SSID ssj0025774
Score 2.424157
Snippet Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse remains...
Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse...
BackgroundAllogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas relapse...
Abstract Background Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is recommended for patients with KMT2A-rearranged (KMT2A-r) leukemia whereas...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
StartPage 605
SubjectTerms 5-aza-2'-deoxycytidine
Acute leukemia
Adolescent
Adult
Aged
Allo-HSCT
Allografts
Blood
Blood platelets
Bone marrow
Busulfan
Cancer
Care and treatment
China - epidemiology
Conditioning
Cyclophosphamide
Cytogenetics
Decitabine
Decitabine - administration & dosage
Decitabine - therapeutic use
Disease prevention
Female
Gene Rearrangement
Graft versus host disease
Graft-versus-host reaction
Hematopoietic Stem Cell Transplantation - methods
Hematopoietic stem cells
Histone-Lysine N-Methyltransferase - genetics
Humans
Intensified conditioning
Irradiation
KMT2A-r leukemia
Leukemia
Leukemia - therapy
Male
Medical diagnosis
Medical prognosis
Middle Aged
Myeloid-Lymphoid Leukemia Protein - genetics
Neutrophils
Patient outcomes
Patients
Relapse
Remission (Medicine)
Retrospective Studies
Stem cell transplantation
Stem cells
Subgroups
Survival
Toxicity
Transplantation
Transplantation Conditioning - methods
Transplantation, Homologous - methods
Transplants & implants
Young Adult
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Lj9MwELbQHhAXxJvAAkZC4oCitR3bcbgVxGoFKqddaW-WPXZFRTddpemBP8VvZOwkVSMOXDhVradV7Xl944w_E_JOaQeOcaxOGmVKGSCWjWtCCTzUgfEYed4aWH7XF1fy67W6PrrqK_WEDfTAw8KdrTzX4GqtXECozJRn4J1rKgMgEK3k6Is5byqmxlJLIaqZjsgYfbbDrMZTs60sGZZkrGSzNJTZ-v-OyUdJad4weZSBzh-Q-yN0pIvhLz8kd2L7iNxdjg_HH5PfYzv6ClElxTI3rMfN1vSmH26CoCHCundYDkeaGjL2OzptJtCbX3GzdX6TqcDnP4DIlmamDjrysO5o2sCl35aXYlF2qd83HVIIdBP3P-PN2n2kjuZexTSX2NEu9t12OtVJM6ftE3J1_uXy80U5XsdQgpK6L6UXWkjnuPMBlSHASwM8hoAvggNA8KJyHjGNAgwLDpqgVHpwa1aRuSpWT8lJu23jc0IlIE4ySgCWl7IBY3TQzgDjXsTaRFOQD5N27O3AumFztWK0HXRpUZc269KygnxKCjxIJsbs_AHakR3tyP7LjgryJqnfDsdPD35vFwZBkFGNqQryPkskz0crADceYMApJQ6tmeTpTBI9FubDk4nZMWLsbMXTXe-1VDidt4fh9M3UBdfG7T7LsErimsqCPBss8jBpxJWVrgUunZnZ6mxV5iPt-kfmE-dcY9SW-sX_WMeX5J5Ifpa5ME_JSd_t4yvEbb1_nV30Dx-2RSo
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: ProQuest Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1Lb9QwELagSIgL4k2ggJGQOKCotmM7Dhe0IKoKtJxaaW-WXwsrtpuSzR76p_obGTvOthESp1XWk8j2PDwzHn9G6J2QxhlCITpphCq5d6FsTONLR33tCQ2BptTA_Ic8OePfFmKRE27bXFY52sRkqH3rYo78qKLxLuyaC_Lp4k8Zb42Ku6v5Co3b6E6ELotSXS-uAy4Bvs14UEbJoy2sbTSW3PKSQGBGSjJZjBJm_7-W-cbSNC2bvLEOHT9A97MDiWcDxx-iW2HzCN2d5y3yx-gqF6UvwbfEEOz6VU65xod-uA8C--BWvYGgOOBYlrHb4jGlgM8vw7o1dp0AwacfAP8WJ7wOnNFYtzimcfH3-SmblV2s-o1HFTxeh93vcL4yH7HBqWIxjiV0uAt9145nO3FCtn2Czo6_nn45KfOlDKUTXPYlt0wybgw11hsvmbNcORq8hx9GnXPesspY8GyEA-NgXOOFiNu3ahmIqUL1FB1s2k14jjB34C0pwRwEmbxxSkkvjXKEWhZqFVSBPozc0RcD9oZOMYuSeuClBl7qxEtNCvQ5MnBPGXGz0x9t91NnNdRLS6UztRTQdc6IsMRZY5pKOeg8OHsFehPZr4dDqHvt1zMFrpASjaoK9D5RRP0HKXAmH2OAIUUkrQnl4YQS9NZNm0cR09lubPW1lBfo7b45vhlr4Tah3SUaUnGYU16gZ4NE7gcN3mUlawZTpyayOpmVactm9SuhilMqwXZz-eL__XqJ7rGoQQnr8hAd9N0uvAK_rLevk_L9BYI1PGY
  priority: 102
  providerName: ProQuest
Title Intensified conditioning containing decitabine versus standard myeloablative conditioning for adult patients with KMT2A-rearranged leukemia: a multicenter retrospective study
URI https://www.ncbi.nlm.nih.gov/pubmed/39736728
https://www.proquest.com/docview/3152697450
https://www.proquest.com/docview/3150345284
https://pubmed.ncbi.nlm.nih.gov/PMC11687046
https://doaj.org/article/fb16ca765ad64205b0cbaa938cc21612
Volume 22
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV3di9QwEA_nHYgv4rfVc40g-CDVJk3SVBDZlTsOZQ85bmHxJeRrdXFvq90ueP-Uf6OTtF2ueC--bNkmLU1mJjOTzPwGoZdcaKszAt5JyWXKnPVpqUuXWuIKlxHvSdwamJ6Kkxn7NOfzPdSXO-omcHOtaxfqSc3q1Zvfvy4_gMC_jwIvxdsN6CwSQmlZmoHDlaXgwh-AZipCRYMp250qAHdGVGYwwklagB7sk2iufcdAUUU8_39X7StqaxhSeUVHHd9BtzvjEo9bbriL9vz6Hro57Y7P76M_XcD6AuxODI6wW3bbseFP09aKwM7bZaPBYfY4hGxsN7jfbsAXl35VabOKYOHDF4DtiyOWB-6QWjc4bPHiz9NzOk7rEBEc0hgcXvntD3-x1O-wxjGaMYzF17j2TV31eZ84ot4-QLPjo_OPJ2lXsCG1nIkmZYYKyrQm2jjtBLWGSUu8c3ChxFrrDM21AauHW1g4tC0d5-FoVy58pnOfP0T762rtHyPMLFhSklMLDigrrZTCCS1tRgz1hfQyQa976qifLS6Hiv6MFKqlpQJaqkhLlSVoEgi46xkwteONqv6mOhFVC0OE1YXg8OmMZtxk1mhd5tLCx4MhmKDngfyqTVDdrQxqLMFMkryUeYJexR6BW4ELrO5SHGBIAWVr0PNw0BNk2g6bexZTvUionIRq8AXjMJwXu-bwZIiTW_tqG_tkOYM5ZQl61HLkbtBgeeaioDB1csCrg1kZtqyX3yPiOCEC1nUmnvzXrD9Ft2gQqAiLeYj2m3rrn4EJ15gRulHMixE6mBydfjkbxY2QUZRV-D2bfP0L8bZJpw
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtR3bbtMw1BpDAl4QdwKDGQnEA4pmO7bjICFULlNH1z110t6MY7tQ0TWjTYX2U_tGjp2kW4TE256ixqeR7XN8bj4XhF4LaawhFKyTQqiUO-vTwhQutdTljlDvaXQNjI_k8Jh_OxEnW-iiy4UJYZUdT4yM2lU2-Mj3Mhp6YedckI9nv9PQNSrcrnYtNBqyGPnzP2CyrT4cfAH8vmFs_-vk8zBtuwqkVnBZp7xkknFjqCmdcZLZkitLvXPwYNRa60qWmRJEs7BA3cYWTohw_6imnpjMZ_DdG-gmCF4SjL385NLAE6BLdYk5Su6tQJbSEOLLUwKGIElJT_jFHgH_SoIrorAfpnlF7u3fQ3dbhRUPGgq7j7b84gG6NW6v5B-iizYIfgq6LAbj2s1aF2_4UTf9J7DzdlYbMMI9DmEg6xXuXBj49NzPK1POYwHy_gdAn8axPghuq7-ucHAb49F4wgbpMkQZh9QIh-d-_cufzsx7bHCMkAxr8Uu89PWy6nJJcayk-wgdXwu6HqPtRbXwTxHmFrQzJZgFo5YXVinppFGW0JL5XHmVoHcddvRZU-tDRxtJSd3gUgMudcSlJgn6FBC4gQx1uuOLavlDt8deT0sqrcmlgKlzRkRJbGlMkSkLkwflMkG7Af26SXrdcBs9UKB6KVGoLEFvI0TgN0AF1rRpE7CkULmrB7nTgwQ-YfvDHYnplk-t9OWpStCrzXD4Z4i9W_hqHWFIxmFPeYKeNBS5WTRos5nMGWyd6tFqb1f6I4vZz1jFnFIJsoLLZ_-f1y66PZyMD_XhwdHoObrDwmmKdTZ30Ha9XPsXoBPW5ct4EDH6ft0n_y8a-HsJ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Intensified+conditioning+containing+decitabine+versus+standard+myeloablative+conditioning+for+adult+patients+with+KMT2A-rearranged+leukemia%3A+a+multicenter+retrospective+study&rft.jtitle=BMC+medicine&rft.au=Hu%2C+Zhongli&rft.au=Feng%2C+Zinan&rft.au=Liu%2C+Shiqi&rft.au=He%2C+Hai&rft.date=2024-12-31&rft.issn=1741-7015&rft.eissn=1741-7015&rft.volume=22&rft.issue=1&rft_id=info:doi/10.1186%2Fs12916-024-03830-0&rft.externalDBID=n%2Fa&rft.externalDocID=10_1186_s12916_024_03830_0
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1741-7015&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1741-7015&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1741-7015&client=summon