Meta-Analysis of Randomised Clinical Trials Comparing Idarubicin plus Cytarabine with Daunorubicin plus Cytarabine as the Induction Chemotherapy in Patients with Newly Diagnosed Acute Myeloid Leukaemia

被引:20
作者
Wang, Jing [1 ]
Yang, Yong-Gong [1 ]
Zhou, Min [1 ]
Xu, Jing-Yan [1 ]
Zhang, Qi-Guo [1 ]
Zhou, Rong-Fu [1 ]
Chen, Bing [1 ]
Ouyang, Jian [1 ]
机构
[1] Nanjing Univ, Dept Hematol, Affiliated DrumTower Hosp, Sch Med, Nanjing 210008, Jiangsu, Peoples R China
来源
PLOS ONE | 2013年 / 8卷 / 04期
关键词
ACUTE MYELOGENOUS LEUKEMIA; 1ST COMPLETE REMISSION; HIGH-DOSE DAUNORUBICIN; PUBLICATION BIAS; ADULT PATIENTS; THERAPY; MULTICENTER; COMBINATION; RECOMMENDATIONS; FLUDARABINE;
D O I
10.1371/journal.pone.0060699
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: To determine whether the use of idarubicin+cytarabine (IA) is more effective than the use of daunorubicin+cytarabine (DA) as induction chemotherapy for patients with newly diagnosed acute myeloid leukaemia. Methods: A computer-based search was performed. Randomised trials comparing IA with DA as induction therapy for newly diagnosed AML were included in this meta-analysis. The primary outcome of interest for our analysis was survival (disease-free survival, event-free survival and overall survival); the secondary endpoint was complete remission. Results: Ten trials with 4,060 patients were eligible for this meta-analysis. Our pooled results suggest that IA is associated with a significant advantage in CR (RR = 1.23; 95% CI = 1.07-1.41, p = 0.004), EFS (HR = 0.64; 95% CI = 0.45-0.91, p = 0.013), and OS (HR = 0.88; 95% CI = 0.81-0.95, p = 0.02) but not in DFS (HR = 0.90; 95% CI = 0.80-1.00, p = 0.06). In the subgroup analysis, age had a significant interaction with OS and CR benefits. Conclusion: Our analysis indicated that IA could improve the duration of overall survival compared to DA as induction therapy for young patients with newly diagnosed AML. Further study is needed to determine whether IA can produce clinical benefits in selected genetic or molecular subgroups of young AML patients.
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页数:9
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