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基于治疗药物监测的个体化艾曲泊帕在儿童免疫性血小板减少症中的应用探索性研究。

Exploratory study on the individualized application of eltrombopag in paediatric immune thrombocytopenia guided by therapeutic drug monitoring.

机构信息

Hematology Oncology Center, Beijing Children's Hospital, Capital Medical University, Beijing, China.

Department of Pharmacy, Beijing Children's Hospital, Capital Medical University, Beijing, China.

出版信息

Br J Haematol. 2024 Nov;205(5):1930-1937. doi: 10.1111/bjh.19735. Epub 2024 Sep 2.

Abstract

There are variations in individual eltrombopag concentrations that may impact efficacy and adverse drug reactions (ADRs) in paediatric immune thrombocytopenia (ITP). To solve this problem, we tailored the eltrombopag dosage refer to concentration, then followed up to assess concentration value in paediatric ITP. This is a single-centre, prospective, observational study. The eltrombopag dosage was adjusted, and children were divided into three groups: the maintenance, discontinuation, and increase groups. Concentration and other data were compared to explore concentration value in guiding the individualized treatment of paediatric ITP. Thirty-nine patients were enrolled, including 23 in the maintenance group, 3 in the discontinued group and 13 in the increase group. 3 patients discontinued eltrombopag due to ADRs, which was significantly higher than patients in the maintenance group (t = 3.606, p = 0.001). In all, 13 patients increased their dosage due to poor response, whose concentration and platelet count were significantly lower than patients in the maintenance group (t = 2.461, p = 0.019; t = 4.633, p < 0.001). Two months after the increase, the number of patients reaching CR and R respectively increased by 2 and 3, while the median platelet count was significantly raised (Z = -2.411, p = 0.016). Concentration could be used as a reference index for the individualized treatment of eltrombopag in paediatric ITP.

摘要

个体依泊帕的浓度存在差异,可能会影响儿童免疫性血小板减少症 (ITP) 的疗效和药物不良反应 (ADR)。为了解决这个问题,我们根据浓度调整了依泊帕的剂量,然后进行随访以评估儿童 ITP 中的浓度值。这是一项单中心、前瞻性、观察性研究。调整了依泊帕的剂量,将儿童分为三组:维持组、停药组和加量组。比较了浓度和其他数据,以探讨浓度值在指导儿童 ITP 个体化治疗中的作用。共纳入 39 例患者,其中维持组 23 例,停药组 3 例,加量组 13 例。3 例患者因 ADR 停止使用依泊帕,明显高于维持组患者(t=3.606,p=0.001)。共有 13 例患者因反应不佳而增加剂量,其浓度和血小板计数明显低于维持组患者(t=2.461,p=0.019;t=4.633,p<0.001)。增加剂量后 2 个月,达到完全缓解和部分缓解的患者数分别增加了 2 例和 3 例,血小板计数中位数明显升高(Z=-2.411,p=0.016)。浓度可作为儿童 ITP 依泊帕个体化治疗的参考指标。

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