Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
Department of Gastroenterology and Hepatology, Japanese Red Cross Society Musashino Hospital, Musashino, Japan.
Clin Gastroenterol Hepatol. 2019 May;17(6):1192-1200. doi: 10.1016/j.cgh.2018.11.047. Epub 2018 Nov 28.
BACKGROUND & AIMS: Platelet transfusion is used to prevent hemorrhagic events in patients with thrombocytopenia undergoing invasive procedures, but there are many disadvantages. We evaluated the efficacy and safety of lusutrombopag in patients with chronic liver disease and thrombocytopenia undergoing invasive procedures.
We performed a double-blind, parallel-group, phase 3 study of 96 patients with chronic liver disease and thrombocytopenia (platelet counts below 50,000/μL) undergoing invasive procedures from October 2013 to May 2014 at 81 centers in Japan. Patients were randomly assigned (1:1) to groups given once-daily lusutrombopag (3 mg) or placebo for up to 7 days. The primary efficacy endpoint was the proportion of patients not requiring platelet transfusion before the invasive procedure. The protocol-defined response (platelet count 50,000/μL or more with an increase of 20,000/μL or more from baseline) and the time course of the change in platelet count were also evaluated. Adverse events were recorded.
The proportions of patients who did not require preoperative platelet transfusion were 79.2% (38/48) in the lusutrombopag group and 12.5% (6/48) in the placebo group (P < .0001). A response was observed in 77.1% (37/48) of patients in the lusutrombopag group and 6.3% (3/48) of patients in the placebo group (P < .0001). In the lusutrombopag group without platelet transfusion, the median platelet count was 50,000/μL or more after 5 days; the mean time to reach the maximum platelet count was 13.4 days; and the number of days (adjusted mean) during which the platelet count was 50,000/μL or more was 21.09 days. Adverse drug reactions were reported in 8.3% of patients in the lusutrombopag group and 2.1% of patients in the placebo group. Two patients (1 per group) had a thrombotic event, but neither were associated with an excessive increase in platelet count (200,000/μL or more).
In a placebo-controlled trial, lusutrombopag was effective in achieving and maintaining the target platelet count in patients with chronic liver disease and thrombocytopenia undergoing invasive procedures. No significant safety concerns were raised. Japanese clinical trial registration no: JapicCTI-132323.
血小板输注用于预防接受有创操作的血小板减少症患者发生出血事件,但存在许多缺点。我们评估了 lusutrombopag 在接受有创操作的慢性肝病和血小板减少症(血小板计数<50,000/μL)患者中的疗效和安全性。
我们在日本 81 个中心进行了一项 96 例慢性肝病和血小板减少症(血小板计数<50,000/μL)患者的双盲、平行组、3 期研究,这些患者于 2013 年 10 月至 2014 年 5 月期间接受有创操作。患者按 1:1 随机分为 lusutrombopag(3 mg)组或安慰剂组,每天一次,最多用药 7 天。主要疗效终点是在接受有创操作前无需血小板输注的患者比例。还评估了方案定义的反应(血小板计数 50,000/μL 或更高,且与基线相比增加 20,000/μL 或更高)和血小板计数变化的时间过程。记录不良事件。
lusutrombopag 组 48 例患者中 79.2%(38/48)无需术前血小板输注,安慰剂组为 12.5%(6/48)(P<0.0001)。 lusutrombopag 组 77.1%(37/48)的患者有反应,安慰剂组为 6.3%(3/48)(P<0.0001)。在无需血小板输注的 lusutrombopag 组中,中位血小板计数在 5 天后达到 50,000/μL 或更高;达到最大血小板计数的平均时间为 13.4 天;血小板计数达到 50,000/μL 或更高的天数(调整均值)为 21.09 天。 lusutrombopag 组 8.3%的患者和安慰剂组 2.1%的患者报告有药物不良反应。2 例患者(每组 1 例)发生血栓事件,但均与血小板计数过度增加(200,000/μL 或更高)无关。
在安慰剂对照试验中, lusutrombopag 可有效实现并维持接受有创操作的慢性肝病和血小板减少症患者的目标血小板计数,且未出现显著的安全性问题。日本临床试验注册编号:JapicCTI-132323。