Department of Pediatrics, Faculty of Medicine, Saint George Hospital University Medical Center, Balamand University, Beirut, Lebanon.
Department of Pediatric Hematology Oncology, School of Medicine, Byblos, and Nini Hospital, Lebanese American University, Tripoli, Lebanon.
Ann Hematol. 2022 May;101(5):991-997. doi: 10.1007/s00277-022-04804-z. Epub 2022 Mar 12.
About 20% to 30% of pediatric patients with immune thrombocytopenia (ITP) develop chronic or refractory disease lasting 12 months or more that can be challenging to treat. Eltrombopag is being used after failure of previous lines of therapy with good results at tertiary healthcare centers in Lebanon, a developing country with available multidisciplinary treatment modalities. This is a retrospective multicenter observational study that analyzed data on pediatric patients with chronic or refractory ITP who were given eltrombopag as second- or third-line therapy in 6 large referral hospitals in Beirut (country capital located in mid Lebanon), South, North, and Mount Lebanon between October 2016 and May 2020. The primary end point of the study was a proportion of patients achieving platelet counts of ≥ 50 × 10/L for at least 6 weeks without requiring rescue therapy during the observation period. Data from 36 patients treated for chronic and refractory ITP, 20 (55.6%) males and 16 (44.4%) females, were analyzed. The median age at the eltrombopag dose was 11 years (2-18 years). All the patients had failure of the first-line therapy with steroids, 3 patients received eltrombopag as second-line therapy, and the remaining patients had failure of at least 2 previous lines of therapy, including steroids. The primary end point was achieved in 21 (58.3%) of 36 patients. The treatment was discontinued in 3 patients due to no response. Hepatotoxicity and all other adverse events (headache, weakness, and diarrhea) were mild and transient. All the patients who achieved the target platelet count of ≥ 50 × 10/L maintained the response for the treatment duration, which was a minimum of 5 months up to 3 years, with median/mean observation periods of 12 months and 14 months, respectively. This study confirms the findings of randomized controlled trials that eltrombopag as second- or third-line therapy in pediatric patients with chronic and refractory ITP is effective and safe, reinforcing its role in the real-world management of these patients.
约 20%至 30%患有免疫性血小板减少症 (ITP)的儿科患者会发展为持续 12 个月或更长时间的慢性或难治性疾病,这可能难以治疗。在黎巴嫩的三级保健中心,在前一线治疗失败后,使用艾曲波帕治疗取得了良好的效果,而黎巴嫩是一个拥有多种多学科治疗方式的发展中国家。这是一项回顾性多中心观察性研究,分析了 2016 年 10 月至 2020 年 5 月期间在贝鲁特 (位于黎巴嫩中部的该国首都)、南部、北部和黎巴嫩山的 6 家大型转诊医院接受艾曲波帕作为二线或三线治疗的慢性或难治性 ITP 儿科患者的数据。该研究的主要终点是在观察期间无需抢救治疗即可达到血小板计数至少为 50×10/L 且持续至少 6 周的患者比例。分析了 36 例接受慢性和难治性 ITP 治疗的患者的数据,其中 20 例(55.6%)为男性,16 例(44.4%)为女性。艾曲波帕剂量的中位年龄为 11 岁(2-18 岁)。所有患者在前一线类固醇治疗失败后,3 例患者接受了艾曲波帕作为二线治疗,其余患者在前一线治疗至少失败 2 次,包括类固醇。36 例患者中的 21 例(58.3%)达到了主要终点。由于无反应,有 3 例患者停止了治疗。肝毒性和所有其他不良事件(头痛、乏力和腹泻)均为轻度和短暂的。所有达到血小板计数≥50×10/L 目标的患者在治疗期间均保持了反应,治疗持续时间最短为 5 个月,最长为 3 年,中位/平均观察期分别为 12 个月和 14 个月。这项研究证实了随机对照试验的结果,即艾曲波帕作为二线或三线治疗慢性和难治性 ITP 的儿科患者是有效和安全的,这加强了它在这些患者的实际管理中的作用。