The impact of different FLT3-inhibitors on overall survival of de novo acute myeloid leukemia: A network meta-analysis

IF 2.1 4区 医学 Q3 HEMATOLOGY
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引用次数: 0

Abstract

FLT3 inhibitors combined with chemotherapy are the standard of care for newly diagnosed FLT3-mutated acute myeloid leukemia (AML). However, no head-to-head studies have established the superiority of one FLT3 inhibitor over another. We conducted a network meta-analysis (NMA) to evaluate overall survival (OS) among different FLT3 inhibitors. Three relevant randomized controlled trials (RCTs), involving 1.358 patients treated with midostaurin, quizartinib, and sorafenib, were included in our analysis. The hazard ratios (HRs) revealed no significant differences in OS between midostaurin and quizartinib (HR, 1.00; 95 % CI, 0.73–1.36), midostaurin and sorafenib (HR, 0.97; 95 % CI, 0.52–1.84), or quizartinib and sorafenib (HR, 0.97; 95 % CI, 0.51–1.85). This NMA, the first to explore this issue, found no OS differences among the different FLT3 inhibitors. In the absence of direct comparison trials, our findings provide practical insights for clinical decision-making.

不同FLT3抑制剂对新发急性髓性白血病总生存期的影响:网络荟萃分析
FLT3抑制剂联合化疗是治疗新诊断的FLT3突变急性髓性白血病(AML)的标准疗法。然而,目前还没有头对头研究证实一种FLT3抑制剂优于另一种FLT3抑制剂。我们进行了一项网络荟萃分析(NMA),以评估不同FLT3抑制剂的总生存期(OS)。我们的分析纳入了三项相关的随机对照试验(RCT),涉及接受米哚妥林、奎沙替尼和索拉非尼治疗的 1,358 名患者。危险比(HR)显示,米哚妥林与奎沙替尼(HR,1.00;95 % CI,0.73-1.36)、米哚妥林与索拉非尼(HR,0.97;95 % CI,0.52-1.84)或奎沙替尼与索拉非尼(HR,0.97;95 % CI,0.51-1.85)的OS无显著差异。该NMA是首次探讨这一问题的研究,它发现不同的FLT3抑制剂在OS方面没有差异。在缺乏直接对比试验的情况下,我们的研究结果为临床决策提供了实用的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Leukemia research
Leukemia research 医学-血液学
CiteScore
4.00
自引率
3.70%
发文量
259
审稿时长
1 months
期刊介绍: Leukemia Research an international journal which brings comprehensive and current information to all health care professionals involved in basic and applied clinical research in hematological malignancies. The editors encourage the submission of articles relevant to hematological malignancies. The Journal scope includes reporting studies of cellular and molecular biology, genetics, immunology, epidemiology, clinical evaluation, and therapy of these diseases.
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