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Efficacy and toxicity of cladribine for the treatment of refractory acute myeloid leukemia: a meta-analysis

机译:克拉屈滨治疗难治性急性髓细胞白血病的疗效和毒性:一项荟萃分析

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Purpose: To investigate the overall efficacy and toxicity of cladribine and cladribine-based chemotherapy in the treatment of patients with refractory acute myeloid leukemia (AML) based on meta-analysis. Methods: PubMed, EMBASE database, and the Cochrane Library were searched for relevant studies. Eligible studies were clinical trials of refractory AML assigned to cladribine with data on efficacy including complete remission (CR) rate, overall response rate (ORR) and overall survival. Toxicity was evaluated based on the early death rate and the incidence of grade 3 and 4 adverse events (AEs). Results: A total of 10 clinical trials including 422 refractory AML patients were analyzed. The overall CR rate was 42.2% (95% CI: 31.0–54.3%). And the ORR of seven trials including 235 patients was 49.7% (95% CI: 33.5–66.0%). The overall early death rate of 260 patients enrolled in five trials was 6.8% (95% CI: 4.3–10.6%). Thrombocytopenia, anemia, neutropenia, and infection were the most common grade 3 and 4 AEs. Conclusion: Cladribine is effective for refractory AML, and its efficacy can be increased with the combination of cladribine, cytarabine, and granulocyte-colony stimulating factor regimen.
机译:目的:基于荟萃分析,研究克拉屈滨和克拉屈滨为基础的化学疗法治疗难治性急性髓细胞白血病(AML)患者的整体疗效和毒性。方法:检索PubMed,EMBASE数据库和Cochrane库以进行相关研究。合格的研究是分配给克拉屈滨的难治性AML临床试验,其疗效数据包括完全缓解(CR)率,总缓解率(ORR)和总生存期。根据早期死亡率以及3级和4级不良事件(AE)的发生率评估毒性。结果:共分析了10项临床试验,包括422例难治性AML患者。总体CR率为42.2%(95%CI:31.0-54.3%)。包括235名患者在内的7项试验的ORR为49.7%(95%CI:33.5-66.0%)。参加五项试验的260名患者的总早期死亡率为6.8%(95%CI:4.3-10.6%)。血小板减少,贫血,中性粒细胞减少和感染是最常见的3级和4级AE。结论:克拉屈滨治疗难治性AML有效,克拉屈滨,阿糖胞苷,粒细胞集落刺激因子联合治疗可提高疗效。

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