Dong Shuyue, Wang Zhifa, Wang Nan, Ma Jingyao, Meng Jinxi, Sun Yixin, Cheng Xiaoling, Wu Runhui
Hematology Oncology Center Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Department of Pharmacy Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Pediatr Investig. 2024 Jan 29;8(1):44-52. doi: 10.1002/ped4.12411. eCollection 2024 Mar.
Eltrombopag has been recommended for pediatric immune thrombocytopenia (ITP). Response and adverse drug reactions (ADRs) varied widely between individuals, even at the same dose of eltrombopag. The appropriate eltrombopag concentration in ITP has not been reported.
This study aims to explore the appropriate eltrombopag concentration in pediatric ITP.
This was a single-center, prospective cohort study. Children diagnosed with refractory persistent/chronic ITP and platelet count < 30×10/L were treated with eltrombopag and followed up for at least 2 months. Concentration was detected by high-performance liquid chromatography-mass spectrometry at least 2 weeks after eltrombopag. The clinical characteristics-concentration, concentration-response, and concentration-ADRs were analyzed.
A total of 30 patients were enrolled, comprising 13 males and 17 females, with a median age of 72 (45‒94) months. The median dose and concentration were 1.39 (1.09‒1.56) mg/kg and 2.70 (2.25‒4.13) mg/L, respectively. Of the enrolled patients, 14 responded to treatment, whereas 16 did not. Additionally, five experienced adverse drug reactions. No linear correlation was observed between eltrombopag concentration and clinical characteristics. The concentration was lower in the response group than in the nonresponse group, but there was no significant difference ( = 0.755, = 0.457). Patients who experienced ADRs had a higher concentration than those without ADRs ( = 2.538, = 0.017). The area under the receiver operating characteristic curve of ADRs was 0.78 (95% confidence interval: 0.56‒1.00). Youden's index identified the cutoff point as 4.33 mg/L, with a sensitivity of 88% and a specificity of 60%. Logistic regression analysis demonstrated that a higher platelet count before eltrombopag predicted a favorable response.
Eltrombopag proves efficacious and well-tolerated for treating pediatric ITP. However, prolonged and high-dose administration may increase the likelihood of ADRs. Thus, examining the appropriate eltrombopag concentration assists in directing individualized management of pediatric ITP.
艾曲泊帕已被推荐用于治疗儿童免疫性血小板减少症(ITP)。即使使用相同剂量的艾曲泊帕,个体之间的反应和药物不良反应(ADR)差异也很大。目前尚未报道ITP患者中艾曲泊帕的合适浓度。
本研究旨在探索儿童ITP患者中艾曲泊帕的合适浓度。
这是一项单中心前瞻性队列研究。对诊断为难治性持续性/慢性ITP且血小板计数<30×10⁹/L的儿童使用艾曲泊帕进行治疗,并随访至少2个月。在使用艾曲泊帕至少2周后,采用高效液相色谱-质谱法检测浓度。分析临床特征-浓度、浓度-反应及浓度-ADR之间的关系。
共纳入30例患者,其中男性13例,女性17例,中位年龄为72(45 - 94)个月。中位剂量和浓度分别为1.39(1.09 - 1.56)mg/kg和2.70(2.25 - 4.13)mg/L。纳入的患者中,14例治疗有效,16例无效。此外,5例出现药物不良反应。未观察到艾曲泊帕浓度与临床特征之间存在线性相关性。反应组的浓度低于无反应组,但差异无统计学意义(P = 0.755,95%CI = 0.457)。出现ADR的患者浓度高于未出现ADR的患者(P = 2.538,95%CI = 0.017)。ADR的受试者工作特征曲线下面积为0.78(95%置信区间:0.56 - 1.00)。约登指数确定的截断点为4.33mg/L,灵敏度为88%,特异度为60%。逻辑回归分析表明,使用艾曲泊帕前较高的血小板计数预示着良好的反应。
艾曲泊帕被证明对治疗儿童ITP有效且耐受性良好。然而,长期高剂量给药可能会增加ADR的发生可能性。因此,检测艾曲泊帕的合适浓度有助于指导儿童ITP的个体化管理。