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新型多激酶抑制剂SAR103168用于难治性/复发性急性白血病或高危骨髓增生异常综合征患者的I期试验

Phase I trial of SAR103168, a novel multi-kinase inhibitor, in patients with refractory/relapsed acute leukemia or high-risk myelodysplastic syndrome.

作者信息

Roboz Gail J, Khoury H Jean, Jabbour Elias, Session Wilena, Ritchie Ellen K, Miao Harry, Faderl Stefan, Zheng Wei, Feldman Eric J, Arellano Martha, Morrison J Gilmour, Ravandi Farhad

机构信息

Department of Medicine, Weill Medical College of Cornell University , New York, NY , USA.

出版信息

Leuk Lymphoma. 2015 Feb;56(2):395-400. doi: 10.3109/10428194.2014.918970.

Abstract

There is no effective treatment for relapsed/refractory acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS). We conducted a phase I dose escalation trial of SAR103168, a novel multi-targeted kinase inhibitor with activity against the Src kinase family, the BCR-Abl kinase and several angiogenic receptor kinases. Twenty-nine patients 18-83 years old were treated with SAR103168. Pharmacokinetics was characterized by plasma peak concentration (Cmax) at the end of the infusion, followed by a biphasic decline in the elimination profile. Adverse events were as expected for the patient population and there were no individual toxicities specific to SAR103168. Due to the unpredictable nature of drug exposure, the sponsor decided to discontinue the study prior to reaching the maximum tolerated dose.

摘要

对于复发/难治性急性髓系白血病(AML)或骨髓增生异常综合征(MDS),目前尚无有效的治疗方法。我们开展了一项关于SAR103168的I期剂量递增试验,SAR103168是一种新型多靶点激酶抑制剂,对Src激酶家族、BCR-Abl激酶和几种血管生成受体激酶具有活性。29名年龄在18至83岁的患者接受了SAR103168治疗。药代动力学特征为输注结束时的血浆峰浓度(Cmax),随后消除曲线呈双相下降。不良事件与该患者群体预期的情况一致,且没有SAR103168特有的个体毒性。由于药物暴露的不可预测性,申办方决定在达到最大耐受剂量之前停止该研究。

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