Suga Takayoshi, Kakizaki Satoru, Naganuma Atsushi, Hatanaka Takeshi, Takakusagi Satoshi, Takizawa Daichi, Arai Hirotaka, Ueno Takashi, Iizuka Keisuke, Fukuchi Toru, Saito Shuichi, Tojima Hiroki, Yamazaki Yuichi, Uraoka Toshio
Department of Gastroenterology NHO Shibukawa Medical Center Shibukawa Japan.
Department of Clinical Research NHO Takasaki General Medical Center Takasaki Japan.
JGH Open. 2024 Dec 31;9(1):e70081. doi: 10.1002/jgh3.70081. eCollection 2025 Jan.
Oral thrombopoietin receptor agonists are used to treat thrombocytopenia in patients with chronic liver disease who are scheduled for invasive procedures. The efficacy of lusutrombopag based on the pretreatment platelet count was investigated.
Patients treated at nine hospitals from December 2015 to December 2023 were included. Efficacy was assessed by comparing the proportion of patients achieving a platelet count ≥ 50 000/μL and the change in platelet count.
Seventy patients were eligible for evaluation. Patients with a pretreatment platelet count < 40 000/μL had a significantly lower rate of achieving a platelet count of ≥ 50 000/μL than those with a pretreatment count of 40 000-50 000/μL (62.5% vs. 84.2%, = 0.038); however, there was no significant difference in the change in platelet count (25 700 vs. 24 400/μL, = 0.972). Patients with viral-related cirrhosis showed a significantly greater change in platelet count than the others (29 100 vs. 19 200/μL, = 0.012). For patients receiving multiple lusutrombopag treatments, the change in platelet count was significantly lower in the second treatment than in the first treatment (26 900 vs. 20 800/μL, = 0.041). The main adverse event observed was thrombosis (2.9%).
Lusutrombopag increases platelet count regardless of pretreatment levels, but efficacy, defined as achieving a platelet count of ≥ 50 000/μL, may be insufficient in patients with a pretreatment platelet count < 40 000/μL. Additionally, patients with non-viral liver disease responded less well to treatment compared to those with viral liver disease. Therefore, treatment strategies should be tailored based on pretreatment platelet counts and the etiology of liver disease.
口服血小板生成素受体激动剂用于治疗计划接受侵入性操作的慢性肝病患者的血小板减少症。研究了基于治疗前血小板计数的芦曲泊帕的疗效。
纳入2015年12月至2023年12月在9家医院接受治疗的患者。通过比较血小板计数≥50000/μL的患者比例和血小板计数变化来评估疗效。
70例患者符合评估条件。治疗前血小板计数<40000/μL的患者达到血小板计数≥50000/μL的比例显著低于治疗前计数为40000-50000/μL的患者(62.5%对84.2%,P=0.038);然而,血小板计数变化无显著差异(25700对24400/μL,P=0.972)。病毒相关性肝硬化患者的血小板计数变化显著大于其他患者(29100对19200/μL,P=0.012)。对于接受多次芦曲泊帕治疗的患者,第二次治疗时血小板计数变化显著低于第一次治疗(26900对20800/μL,P=0.041)。观察到的主要不良事件是血栓形成(2.9%)。
无论治疗前水平如何,芦曲泊帕均可增加血小板计数,但对于治疗前血小板计数<40000/μL的患者,定义为达到血小板计数≥50000/μL的疗效可能不足。此外,与病毒性肝病患者相比,非病毒性肝病患者对治疗的反应较差。因此,应根据治疗前血小板计数和肝病病因制定个性化的治疗策略。