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中剂量罗替尼治疗晚期系统性肥大细胞增多症患者的疗效和安全性:一项 II 期试验的 10 年中位随访。

Efficacy and safety of midostaurin in patients with advanced systemic mastocytosis: 10-year median follow-up of a phase II trial.

机构信息

Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.

Department of Pathology, University of New Mexico, Albuquerque, NM, USA.

出版信息

Leukemia. 2018 Feb;32(2):470-478. doi: 10.1038/leu.2017.234. Epub 2017 Jul 24.

Abstract

Patients with advanced systemic mastocytosis (SM) (e.g. aggressive SM (ASM), SM with an associated hematologic neoplasm (SM-AHN) and mast cell leukemia (MCL)) have limited treatment options and exhibit reduced survival. Midostaurin is an oral multikinase inhibitor that inhibits D816V-mutated KIT, a primary driver of SM pathogenesis. We conducted a phase II trial of midostaurin 100 mg twice daily, administered as 28-day cycles, in 26 patients (ASM, n=3; SM-AHN, n= 17; MCL, n=6) with at least one sign of organ damage. During the first 12 cycles, the overall response rate was 69% (major/partial response: 50/19%) with clinical benefit in all advanced SM variants. With ongoing therapy, 2 patients achieved a complete remission of their SM. Midostaurin produced a ⩾50% reduction in bone marrow mast cell burden and serum tryptase level in 68% and 46% of patients, respectively. Median overall survival for the entire cohort was 40 months, and 18.5 months for MCL patients. Low-grade gastrointestinal side effects were common and manageable with antiemetics. The most frequent grade 3/4 nonhematologic and hematologic toxicities were asymptomatic hyperlipasemia (15%) and anemia (12%). With median follow-up of 10 years, no unexpected toxicities emerged. These data establish the durable activity and tolerability of midostaurin in advanced SM.

摘要

晚期系统性肥大细胞增多症(SM)(例如侵袭性 SM(ASM)、伴相关血液肿瘤的 SM(SM-AHN)和肥大细胞白血病(MCL))患者的治疗选择有限,生存时间缩短。米哚妥林是一种口服多激酶抑制剂,可抑制 SM 发病机制的主要驱动因素 D816V 突变型 KIT。我们开展了一项米哚妥林 100mg 每日两次、28 天为一周期的 26 例患者(ASM 患者 3 例、SM-AHN 患者 17 例、MCL 患者 6 例)的 II 期临床试验,这些患者至少存在一种器官损伤迹象。在前 12 个周期中,整体缓解率为 69%(完全缓解/部分缓解:50/19%),所有晚期 SM 变异型均具有临床获益。在持续治疗中,2 例患者的 SM 完全缓解。米哚妥林使 68%和 46%的患者骨髓肥大细胞负荷和血清胰蛋白酶水平分别降低 ⩾50%。整个队列的中位总生存期为 40 个月,MCL 患者为 18.5 个月。常见且可通过止吐药控制的是低级别胃肠道副作用。最常见的 3/4 级非血液学和血液学毒性是无症状性高脂血症(15%)和贫血(12%)。中位随访 10 年,未出现新的意外毒性。这些数据确立了米哚妥林在晚期 SM 中的持久疗效和耐受性。

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