一项关于FLT3抑制剂在急性髓性白血病治疗使用和反应率的GIMEMA调查:来自意大利现实世界实践的见解。

EJHaem Pub Date : 2024-11-22 DOI:10.1002/jha2.1045
Monica Messina, Alfonso Piciocchi, Leonardo M. Siena, Stefano Soddu, Francesco Buccisano, Cristina Mecucci, Giovanni Martinelli, Antonio Curti, Roberto Cairoli, Paola Fazi, Marco Vignetti, Maria Teresa Voso, Adriano Venditti, Anna Candoni
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摘要

鉴于意大利猫麦克多诺肉瘤(FMS)样酪氨酸激酶3 (FLT3)抑制剂在现实生活中的治疗应用数据有限,我们调查了意大利59个血液学中心的研究人员,以了解接受FLT3抑制剂的急性髓性白血病(AML)患者的比例,并收集了这些药物的疗效和安全性数据。调查结果显示,在现实环境中,3/7 + midoin方案对新诊断的flt3突变AML的反应率和吉特替尼方案对复发/难治性AML的反应率与注册临床试验报告的反应率相当。3/7 + midoin治疗导致63%的完全缓解(CR)率,吉特替尼导致44%的CR率。吉特替尼因不耐受或毒性而停药的比率很低(占治疗病例的4%)。
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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A GIMEMA survey on therapeutic use and response rates of FLT3 inhibitors in acute myeloid leukemia: Insights from Italian real-world practice

Given the limited data on the real-life therapeutic use of feline McDonough sarcoma (FMS)-like tyrosine kinase 3 (FLT3) inhibitors in Italy, we surveyed investigators at 59 Italian hematology centers to gain insight into the proportion of acute myeloid leukemia (AML) patients receiving FLT3 inhibitors and we collected data on the efficacy and safety of these agents. The survey results showed that in the real-life setting the response rate of the 3/7 + midostaurin regimen in newly diagnosed FLT3-mutated AML and of gilteritinib in the relapsed/refractory AML were comparable to that reported in the registrative clinical trials. The 3/7 + midostaurin treatment resulted in a 63% of complete remission (CR) rates and gilteritinib in a 44% of CR rates. The discontinuation rate of gilteritinib for intolerance or toxicity was low (accounting for 4% of treated cases).

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