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艾曲波帕用于治疗慢性特发性血小板减少性紫癜。

Eltrombopag for the treatment of chronic idiopathic thrombocytopenic purpura.

作者信息

Bussel James B, Cheng Gregory, Saleh Mansoor N, Psaila Bethan, Kovaleva Lidia, Meddeb Balkis, Kloczko Janusz, Hassani Habib, Mayer Bhabita, Stone Nicole L, Arning Michael, Provan Drew, Jenkins Julian M

机构信息

Weill Cornell Medical College of Cornell University, New York, NY 10065, USA.

出版信息

N Engl J Med. 2007 Nov 29;357(22):2237-47. doi: 10.1056/NEJMoa073275.

Abstract

BACKGROUND

The pathogenesis of chronic idiopathic thrombocytopenic purpura (ITP) involves antibody-mediated platelet destruction and reduced platelet production. Stimulation of platelet production may be an effective treatment for this disorder.

METHODS

We conducted a trial in which 118 adults with chronic ITP and platelet counts of less than 30,000 per cubic millimeter who had had relapses or whose platelet count was refractory to at least one standard treatment for ITP were randomly assigned to receive the oral thrombopoietin-receptor agonist eltrombopag (30, 50, or 75 mg daily) or placebo. The primary end point was a platelet count of 50,000 or more per cubic millimeter on day 43.

RESULTS

In the eltrombopag groups receiving 30, 50, and 75 mg per day, the primary end point was achieved in 28%, 70%, and 81% of patients, respectively. In the placebo group, the end point was achieved in 11% of patients. The median platelet counts on day 43 for the groups receiving 30, 50, and 75 mg of eltrombopag were 26,000, 128,000, and 183,000 per cubic millimeter, respectively; for the placebo group the count was 16,000 per cubic millimeter. By day 15, more than 80% of patients receiving 50 or 75 mg of eltrombopag daily had an increased platelet count. Bleeding also decreased during treatment in these two groups. The incidence and severity of adverse events were similar in the placebo and eltrombopag groups.

CONCLUSIONS

Eltrombopag increased platelet counts in a dose-dependent manner in patients with relapsed or refractory ITP. (ClinicalTrials.gov number, NCT00102739.)

摘要

背景

慢性特发性血小板减少性紫癜(ITP)的发病机制涉及抗体介导的血小板破坏和血小板生成减少。刺激血小板生成可能是治疗该疾病的有效方法。

方法

我们进行了一项试验,将118例慢性ITP且血小板计数低于每立方毫米30,000的成年人随机分组,这些患者有复发情况或其血小板计数对至少一种ITP标准治疗无效,分别接受口服血小板生成素受体激动剂艾曲泊帕(每日30、50或75毫克)或安慰剂。主要终点是第43天时血小板计数达到每立方毫米50,000或更多。

结果

在每日接受30、50和75毫克艾曲泊帕的组中,分别有28%、70%和81%的患者达到主要终点。在安慰剂组中,11%的患者达到该终点。接受30、50和75毫克艾曲泊帕的组在第43天时的血小板计数中位数分别为每立方毫米26,000、128,000和183,000;安慰剂组的计数为每立方毫米16,000。到第15天时,每日接受50或75毫克艾曲泊帕的患者中超过80%的血小板计数增加。这两组治疗期间出血情况也有所减少。安慰剂组和艾曲泊帕组不良事件的发生率和严重程度相似。

结论

艾曲泊帕使复发或难治性ITP患者的血小板计数呈剂量依赖性增加。(ClinicalTrials.gov编号,NCT00102739。)

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