Title Efficacy of Allogeneic Hematopoietic Stem Cell Transplantation in Intermediate-Risk Acute Myeloid Leukemia Adult Patients in First Complete Remission: A Meta-Analysis of Prospective Studies
Authors Li, Dandan
Wang, Li
Zhu, Honghu
Dou, Liping
Liu, Daihong
Fu, Lin
Ma, Cong
Ma, Xuebin
Yao, Yushi
Zhou, Lei
Wang, Qian
Wang, Lijun
Zhao, Yu
Jing, Yu
Wang, Lili
Li, Yonghui
Yu, Li
Affiliation Chinese Peoples Liberat Army Gen Hosp, Dept Hematol, Beijing, Peoples R China.
Med Coll Chinese PLA, Beijing, Peoples R China.
Peking Univ, Inst Hematol, Peoples Hosp, Dept Hematol, Beijing 100871, Peoples R China.
Peking Univ, Hosp 3, Dept Hematol, Beijing 100871, Peoples R China.
PLA Navy Gen Hosp, Dept Clin Lab, Beijing, Peoples R China.
PLA Navy Gen Hosp, Tumor Diag & Treatment Ctr, Beijing, Peoples R China.
202 Hosp PLA, Dept Hematol, Shenyang, Peoples R China.
Keywords BONE-MARROW-TRANSPLANTATION
ACUTE MYELOGENOUS LEUKEMIA
HIGH-DOSE CYTARABINE
PROSPECTIVE CONTROLLED-TRIAL
PROSPECTIVE MULTICENTER TRIAL
VERSUS-HOST-DISEASE
POSTREMISSION THERAPY
INTENSIFICATION CHEMOTHERAPY
CONSOLIDATION CHEMOTHERAPY
INTENSIVE CHEMOTHERAPY
Issue Date 2015
Publisher PLOS ONE
Citation PLOS ONE.2015,10,(7).
Abstract Hematopoietic stem cell transplantation (HSCT) and consolidation chemotherapy have been used to treat intermediate-risk acute myeloid leukemia (AML) patients in first complete remission (CR1). However, it is still unclear which treatments are most effective for these patients. The aim of our study was to analyze the relapse-free survival (RFS) and overall survival (OS) benefit of allogeneic HSCT (alloHSCT) for intermediate-risk AML patients in CR1. A meta-analysis of prospective trials comparing alloHSCT to non-alloHSCT (autologous HSCT [autoHSCT] and/or chemotherapy) was undertaken. We systematically searched PubMed, Embase, and the Cochrane Library though October 2014, using keywords and relative MeSH or Emtree terms, 'allogeneic'; 'acut*' and 'leukem*/aml/leukaem*/ leucem*/leucaem*'; and 'nonlympho*' or 'myelo*'. A total of 7053 articles were accessed. The primary outcomes were RFS and OS, while the secondary outcomes were treatment-related mortality (TRM) and relapse rate (RR). Hazard ratios (HR) and 95% confidence intervals (CI) were calculated for each outcome. The primary outcomes were RFS and OS, while the secondary outcomes were TRM and RR. We included 9 prospective controlled studies including 1950 adult patients. Patients with intermediate-risk AML in CR1 who received either alloHSCT or non-alloHSCT were considered eligible. AlloHSCT was found to be associated with significantly better RFS, OS, and RR than non-alloHSCT (HR, 0.684 [95% CI: 0.48, 0.95]; HR, 0.76 [95% CI: 0.61, 0.95]; and HR, 0.58 [95% CI: 0.45, 0.75], respectively). TRM was significantly higher following alloHSCT than non-alloHSCT (HR, 3.09 [95% CI: 1.38, 6.92]). However, subgroup analysis showed no OS benefit for alloHSCT over autoHSCT (HR, 0.99 [95% CI: 0.70, 1.39]). In conclusion, alloHSCT is associated with more favorable RFS, OS, and RR benefits (but not TRM outcomes) than non-alloHSCT generally, but does not have an OS advantage over autoHSCT specifically, in patients with intermediate-risk AML in CR1.
URI http://hdl.handle.net/20.500.11897/418178
ISSN 1932-6203
DOI 10.1371/journal.pone.0132620
Indexed SCI(E)
PubMed
Appears in Collections: 第三医院

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