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比较柔红霉素+阿糖胞苷与柔红霉素+阿糖胞苷作为新诊断的急性髓细胞白血病患者诱导化疗的随机临床试验的荟萃分析。

Meta-analysis of randomised clinical trials comparing idarubicin + cytarabine with daunorubicin + cytarabine as the induction chemotherapy in patients with newly diagnosed acute myeloid leukaemia.

机构信息

Department of Hematology, the Affiliated DrumTower Hospital of Nanjing University Medical School, Nanjing, Jiangsu, PR China.

出版信息

PLoS One. 2013 Apr 5;8(4):e60699. doi: 10.1371/journal.pone.0060699. Print 2013.

Abstract

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.

摘要

背景

为了确定柔红霉素+阿糖胞苷(IA)的使用是否比柔红霉素+阿糖胞苷(DA)更有效作为新诊断的急性髓细胞性白血病患者的诱导化疗。

方法

进行了基于计算机的检索。本荟萃分析纳入了比较 IA 与 DA 作为新诊断 AML 诱导治疗的随机试验。我们分析的主要终点是生存(无病生存、无事件生存和总生存);次要终点是完全缓解。

结果

10 项试验共 4060 例患者符合本荟萃分析的条件。我们的汇总结果表明,IA 与 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)和 OS(HR=0.88;95%CI=0.81-0.95,p=0.02)显著相关,但与DFS 无关(HR=0.90;95%CI=0.80-1.00,p=0.06)。亚组分析表明,年龄与 OS 和 CR 获益有显著交互作用。

结论

我们的分析表明,与 DA 相比,IA 可作为年轻新诊断 AML 患者的诱导治疗,改善总生存时间。需要进一步研究确定 IA 是否能在年轻 AML 患者的特定遗传或分子亚组中产生临床获益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86dc/3622517/6cb3be521135/pone.0060699.g001.jpg

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