Evaluation of the Toxicity and Outcomes of the Combination of Midostaurin and CLAG-M in Patients With FLT3-Mutated Acute Myeloid Leukemia (AML): A Multicenter Retrospective Analysis.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Ashley Chen, Grace Baek, Kathryn Russell, Carole Shaw, Megan Othus, Jonathan Cohen, Shannon Palmer, Jack Rasmussen, Joseph Bubalo, Tenzin Tsomo, Tenley Schwarz, Swathi Namburi, Anna Halpern
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引用次数: 0

Abstract

Background: Addition of midostaurin to standard "7+3" (cytarabine and anthracycline) significantly prolongs overall and event-free survival. At University of Washington/Fred Hutchinson Cancer Center (UW/FHCC), the standard regimen for newly diagnosed (ND) and relapsed/refractory (R/R) AML is cladribine, high-dose cytarabine, GCSF, and mitoxantrone (CLAG-M); midostaurin is added if FLT3-mutated. There is limited data on the use of FLT3-inhibitors with high-dose cytarabine regimens in AML.

Objective: This study aimed to evaluate the safety and efficacy of the combination of midostaurin with CLAG-M versus midostaurin plus 7+3 in FLT3-mutated AML patients.

Methods: This is a retrospective, multicenter review including FLT3-mutated AML patients undergoing (re)induction chemotherapy with either CLAG-M or 7+3 at UW/FHCC, Oregon Health & Science University, and Swedish Cancer Institute. The primary outcome was incidence of adverse events. Secondary outcomes included disease response per ELN2017 criteria and 28-day mortality. Excluded were patients on clinical trials or who started midostaurin 30 days after chemotherapy.

Results: Eighty patients treated from September 2016 to December 2023 were included; 36 patients received CLAG-M, and 44 patients 7+3. Baseline characteristics were similar across all institutions. Adverse event rates were similar between the 2 cohorts, except diarrhea and bleeding which were more common in the 7+3 cohort. The rate of complete remission (CR) plus CR with incomplete blood count recovery did not significantly differ between the 2 cohorts: CLAG-M, 86% versus 7+3, 70% (P = 0.11).

Conclusion & relevance: The toxicity profile of CLAG-M combined with midostaurin is comparable with the combination of 7+3 with midostaurin, and induces high remissions rates in adults with FLT3-mutated AML.

评价midoin联合CLAG-M治疗flt3突变急性髓性白血病(AML)患者的毒性和预后:一项多中心回顾性分析
背景:在标准的“7+3”(阿糖胞苷和蒽环类)中加入米多舒林可显著延长总生存期和无事件生存期。在华盛顿大学/弗雷德·哈钦森癌症中心(UW/FHCC),新诊断(ND)和复发/难治性(R/R) AML的标准方案是克拉德里滨、大剂量阿糖胞苷、GCSF和米托蒽醌(CLAG-M);如果flt3突变,则添加midoin。flt3抑制剂与高剂量阿糖胞苷治疗AML的数据有限。目的:本研究旨在评价midoin联合CLAG-M与midoin + 7+3联合治疗flt3突变AML患者的安全性和有效性。方法:这是一项回顾性、多中心的综述,包括在UW/FHCC、俄勒冈健康与科学大学和瑞典癌症研究所接受CLAG-M或7+3(再)诱导化疗的flt3突变AML患者。主要结局是不良事件的发生率。次要结局包括按ELN2017标准的疾病缓解和28天死亡率。排除临床试验患者或化疗后30天开始服药的患者。结果:纳入2016年9月至2023年12月收治的患者80例;CLAG-M 36例,7+3 44例。所有机构的基线特征相似。除了腹泻和出血在7+3队列中更为常见外,两个队列的不良事件发生率相似。完全缓解率(CR)加上不完全血细胞恢复的CR率在两个队列之间没有显著差异:CLAG-M组为86%,而7+ 3,70 % (P = 0.11)。结论及相关性:CLAG-M联合midoschuin的毒性与7+3联合midoschuin相当,并且在成人flt3突变AML患者中具有较高的缓解率。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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