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一项关于急性髓系白血病中FLT3抑制剂治疗用途和缓解率的GIMEMA调查:来自意大利真实世界实践的见解

A GIMEMA survey on therapeutic use and response rates of FLT3 inhibitors in acute myeloid leukemia: Insights from Italian real-world practice.

作者信息

Messina Monica, Piciocchi Alfonso, Siena Leonardo M, Soddu Stefano, Buccisano Francesco, Mecucci Cristina, Martinelli Giovanni, Curti Antonio, Cairoli Roberto, Fazi Paola, Vignetti Marco, Voso Maria Teresa, Venditti Adriano, Candoni Anna

机构信息

Fondazione GIMEMA Rome Italy.

Department of Public Health and Infectious Diseases Sapienza University of Rome Rome Italy.

出版信息

EJHaem. 2024 Nov 22;5(6):1274-1277. doi: 10.1002/jha2.1045. eCollection 2024 Dec.

DOI:10.1002/jha2.1045
PMID:39691247
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11647686/
Abstract

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).

摘要

鉴于意大利关于猫 McDonough 肉瘤(FMS)样酪氨酸激酶 3(FLT3)抑制剂实际治疗应用的数据有限,我们对意大利 59 家血液学中心的研究人员进行了调查,以深入了解接受 FLT3 抑制剂治疗的急性髓系白血病(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,在实际临床中,新诊断的 FLT3 突变型 AML 患者使用 3/7 + 米哚妥林方案以及复发/难治性 AML 患者使用吉瑞替尼的缓解率与注册临床试验中报告的缓解率相当。3/7 + 米哚妥林治疗的完全缓解(CR)率为 63%,吉瑞替尼治疗的 CR 率为 44%。吉瑞替尼因不耐受或毒性而停药的比例较低(占治疗病例的 4%)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0143/11647686/dfa6c06bc9ec/JHA2-5-1274-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0143/11647686/875ce42bb753/JHA2-5-1274-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0143/11647686/dfa6c06bc9ec/JHA2-5-1274-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0143/11647686/875ce42bb753/JHA2-5-1274-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0143/11647686/dfa6c06bc9ec/JHA2-5-1274-g002.jpg

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本文引用的文献

1
Efficacy and toxicity of midostaurin with idarubicin and cytarabine induction in <i>FLT3</I>-mutated acute myeloid leukemia.米哚妥林联合伊达比星及阿糖胞苷诱导治疗FLT3突变型急性髓系白血病的疗效与毒性
Haematologica. 2023 Dec 1;108(12):3460-3463. doi: 10.3324/haematol.2022.281967.
2
Gilteritinib activity in refractory or relapsed FLT3-mutated acute myeloid leukemia patients previously treated by intensive chemotherapy and midostaurin: a study from the French AML Intergroup ALFA/FILO.吉瑞替尼在先前接受过强化化疗和米哚妥林治疗的难治性或复发性FLT3突变急性髓系白血病患者中的活性:来自法国急性髓系白血病协作组ALFA/FILO的一项研究
Leukemia. 2023 Jan;37(1):91-101. doi: 10.1038/s41375-022-01742-7. Epub 2022 Nov 14.
3
Gilteritinib monotherapy for relapsed/refractory FLT3 mutated acute myeloid leukemia: a real-world, multi-center, matched analysis.
吉特替尼单药治疗复发/难治性 FLT3 突变急性髓系白血病:一项真实世界、多中心、匹配分析。
Ann Hematol. 2022 Sep;101(9):2001-2010. doi: 10.1007/s00277-022-04895-8. Epub 2022 Jun 24.
4
Gilteritinib or Chemotherapy for Relapsed or Refractory -Mutated AML.吉特替尼与化疗用于治疗复发/难治性 - 突变型 AML。
N Engl J Med. 2019 Oct 31;381(18):1728-1740. doi: 10.1056/NEJMoa1902688.
5
The REDCap consortium: Building an international community of software platform partners.REDCap 联盟:构建软件平台合作伙伴的国际社区。
J Biomed Inform. 2019 Jul;95:103208. doi: 10.1016/j.jbi.2019.103208. Epub 2019 May 9.
6
Midostaurin plus Chemotherapy for Acute Myeloid Leukemia with a FLT3 Mutation.米哚妥林联合化疗治疗伴有FLT3突变的急性髓系白血病
N Engl J Med. 2017 Aug 3;377(5):454-464. doi: 10.1056/NEJMoa1614359. Epub 2017 Jun 23.
7
Genomics of Acute Myeloid Leukemia Diagnosis and Pathways.急性髓系白血病的诊断与通路的基因组学
J Clin Oncol. 2017 Mar 20;35(9):934-946. doi: 10.1200/JCO.2016.71.2208. Epub 2017 Feb 13.