美度舒林和吉妥珠单抗联合诱导化疗治疗FLT3突变AML的安全性和有效性。

IF 7.1 1区 医学 Q1 HEMATOLOGY
Nigel H Russell, Jad Othman, Oliver Sebastian Cumming, Abin Thomas, Aditya Tedjaseputra, Nicola Potter, Jelena Jovanovic, Amanda Frances Gilkes, Leona Batten, Joanna Canham, Emily L Hinson, Manohursingh Runglall, Phoebe Aucken, Panagiotis Kottaridis, James Durrell Cavenagh, Claire Arnold, Sylvie D Freeman, Mike Dennis, Steven Knapper, Richard James Dillon
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引用次数: 0

摘要

尽管使用了FLT3抑制剂,但由于高复发率,FLT3突变(FLT3mut) AML患者的预后仍然不理想。在英国NCRI AML19试验中,我们评估了柔红霉素、阿糖胞苷(DA)、吉妥珠单抗ozogamicin (GO)和midoshuin (DAGO+m)联合治疗新诊断的年轻FLT3mut AML患者的安全性和有效性。195名患者随机接受DA和一剂或两剂GO (DAGO1和DAGO2)。77例有FLT3突变(60例有FLT3- itd),每次化疗后接受两周midoin治疗,然后维持一年,除非进行移植。midoin联合DAGO1 (DAGO1+m) 39例,DAGO2 (DAGO2+m) 38例。年龄中位数为51岁(20 ~ 74岁),16例(20%)年龄在60 ~ 60岁之间。总有效率(CR + CRi)为91%。第30天和第60天的死亡率为0%,与同时使用DAGO1和DAGO2而不使用midoin的患者相比,毒性没有增加。2y总生存率为77%。2y无事件生存率和累计复发发生率分别为62%和31%。与使用DAGO1和DAGO2不使用midoin治疗的flt3突变AML患者相比,MRD清除率增强。疗程2后,81%的可评估患者外周血NPM1 MRD呈阴性(DAGO2+m为76%,DAGO2+m为86%),79%的患者骨髓FLT3-ITD NGS呈阴性,所有患者FLT3-MRD水平均低于0.01%。DAGO+m安全有效。DAGO2+m现在将在一项随机研究中进行评估(optimize - flt3, ISRCTN 34016918)。试验:ISRCTN78449203。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and Efficacy of Combining Midostaurin and Gemtuzumab Ozogamicin with Induction Chemotherapy in FLT3 mutated AML.

Despite the use of FLT3 inhibitors, outcomes for patients with FLT3 mutated (FLT3mut) AML remain suboptimal because of high rates of relapse. We evaluated the safety and efficacy of the combination of daunorubicin, cytarabine (DA), gemtuzumab ozogamicin (GO) and midostaurin (DAGO+m) for younger patients with newly diagnosed FLT3mut AML in the UK NCRI AML19 trial. 195 patients were randomised to receive DA with either one or two doses of GO (DAGO1 and DAGO2). 77 had a FLT3 mutation (60 had FLT3-ITD) and received midostaurin for two weeks after each chemotherapy course and then as maintainance for one year unless transplanted. 39 patients received midostaurin with DAGO1 (DAGO1+m) and 38 with DAGO2 (DAGO2+m). Their median age was 51y (range 20-74) and 16 (20%) were aged >60y. The overall response rate (CR + CRi) was 91%. Day 30 and day 60 mortality was 0% with no increase in toxicity compared to patients treated contemporaneously with DAGO1 and DAGO2 without midostaurin. 2y overall survival was 77%. 2y event-free survival and cumulative incidence of relapse were 62% and 31% respectively. MRD clearance was enhanced compared to patients with FLT3-mutated AML treated with DAGO1 and DAGO2 without midostaurin. 81% of evaluable patients were NPM1 MRD negative by RT-qPCR in the peripheral blood after course 2 (76% with DAGO1+m and 86% with DAGO2+m), 79% were MRD negative in the bone marrow by FLT3-ITD NGS, and all patients had FLT3-MRD levels below 0.01%. DAGO+m appears safe and effective . DAGO2+m will now be evaluated in a randomised study (OPTIMISE-FLT3, ISRCTN 34016918). Trial: ISRCTN78449203.

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来源期刊
Blood advances
Blood advances Medicine-Hematology
CiteScore
12.70
自引率
2.70%
发文量
840
期刊介绍: Blood Advances, a semimonthly medical journal published by the American Society of Hematology, marks the first addition to the Blood family in 70 years. This peer-reviewed, online-only, open-access journal was launched under the leadership of founding editor-in-chief Robert Negrin, MD, from Stanford University Medical Center in Stanford, CA, with its inaugural issue released on November 29, 2016. Blood Advances serves as an international platform for original articles detailing basic laboratory, translational, and clinical investigations in hematology. The journal comprehensively covers all aspects of hematology, including disorders of leukocytes (both benign and malignant), erythrocytes, platelets, hemostatic mechanisms, vascular biology, immunology, and hematologic oncology. Each article undergoes a rigorous peer-review process, with selection based on the originality of the findings, the high quality of the work presented, and the clarity of the presentation.
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