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口服艾曲波帕治疗日本既往治疗的慢性免疫性血小板减少症患者长达 3 年,安全性和耐受性良好:一项开放标签扩展研究。

Oral eltrombopag for up to three years is safe and well-tolerated in Japanese patients with previously treated chronic immune thrombocytopenia: an open-label, extension study.

机构信息

Hiroshima University, Kasumi 1-2-3, Minami-ku, Hiroshima, Hiroshima, Japan,

出版信息

Int J Hematol. 2013 Sep;98(3):323-30. doi: 10.1007/s12185-013-1401-1. Epub 2013 Jul 30.

DOI:10.1007/s12185-013-1401-1
PMID:23896965
Abstract

Eltrombopag is an oral, nonpeptide, thrombopoietin receptor agonist approved for treatment of chronic immune thrombocytopenia (ITP). The safety, tolerability, and efficacy of eltrombopag for up to 3 years were evaluated in 19 Japanese patients with chronic ITP who had completed a prior 6-month study. Patients received eltrombopag once daily at the last dosage received in the prior study (12.5, 25, or 50 mg). Dose adjustments and treatment interruptions were permitted to maintain platelet counts of 50,000-200,000/μL. Primary evaluations were safety and tolerability of long-term eltrombopag treatment. The median duration of exposure was 27.5 months (range, 9.9-32.3). Adverse events were similar to those reported with short-term use of eltrombopag, and none led to treatment discontinuation. Nine serious adverse events were reported. Median platelet counts began to increase after 1 week of treatment and remained above 50,000/μL for most assessments. Bleeding episodes decreased from 63 % at baseline to 21 % after 2 weeks of treatment and remained below baseline for all assessments. Of 15 patients receiving concomitant baseline ITP medications, 10 permanently discontinued or achieved a sustained reduction of at least one treatment without requiring rescue treatment. Long-term treatment with eltrombopag was safe, well tolerated, and effective in Japanese patients with chronic ITP.

摘要

依洛尤单抗是一种口服、非肽类、血小板生成素受体激动剂,已被批准用于治疗慢性免疫性血小板减少症(ITP)。19 名日本慢性 ITP 患者完成了一项为期 6 个月的研究后,评估了依洛尤单抗长达 3 年的安全性、耐受性和疗效。患者接受依洛尤单抗每日一次治疗,剂量为前研究中最后一次接受的剂量(12.5、25 或 50mg)。允许调整剂量和中断治疗,以维持血小板计数在 50,000-200,000/μL 之间。主要评估指标是长期依洛尤单抗治疗的安全性和耐受性。中位暴露时间为 27.5 个月(范围 9.9-32.3)。不良事件与短期使用依洛尤单抗报告的不良事件相似,且均未导致治疗中断。报告了 9 例严重不良事件。治疗 1 周后血小板计数中位数开始增加,大多数评估时血小板计数保持在 50,000/μL 以上。出血事件从基线时的 63%降至治疗 2 周后的 21%,并且在所有评估时均低于基线。在 15 名接受基线 ITP 药物治疗的患者中,10 名患者永久性停药或在无需抢救治疗的情况下实现了至少一种治疗的持续减少。在日本慢性 ITP 患者中,长期使用依洛尤单抗是安全的,耐受良好且有效。

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