Giordano Paola, Lassandro Giuseppe, Barone Angelica, Cesaro Simone, Fotzi Ilaria, Giona Fiorina, Ladogana Saverio, Miano Maurizio, Marzollo Antonio, Nardi Margherita, Notarangelo Lucia Dora, Pession Andrea, Ruggiero Antonio, Russo Giovanna, Saracco Paola, Spinelli Marco, Tolva Alessandra, Tornesello Assunta, Palladino Valentina, Del Vecchio Giovanni Carlo
Pediatric Unit, Department of Biomedical Science and Human Oncology, University of Bari "Aldo Moro", Bari, Italy.
Department of Pediatric Onco-Hematology, University Hospital of Parma, Parma, Italy.
Front Med (Lausanne). 2020 Feb 28;7:66. doi: 10.3389/fmed.2020.00066. eCollection 2020.
The thrombopoietin receptor agonist eltrombopag has been shown to be safe and effective for children with chronic immune thrombocytopenia (ITP). The aim of the present study was to characterize eltrombopag use in current clinical practice. This is a retrospective multicenter study conducted in 17 centers affiliated to the Italian Association of Pediatric Hematology and Oncology (AIEOP). The primary objective of the study was to determine the prevalence of eltrombopag use in Italian children affected by chronic ITP, after EMA authorization for pediatric age. The secondary objective was to assess efficacy in the first 6 months and safety during the whole period of eltrombopag treatment in current clinical practice. A total of 386 children with chronic ITP were retrospectively enrolled and eligible for analysis. Among these patients, 71 received eltrombopag. The prevalence of eltrombopag use was 19% (95% CI 0.15-0.23). Thirty-one patients (44%) were male and 40 patients (56%) were female. The median age at the first dose of eltrombopag was 12 years (3-17 years). The median duration of eltrombopag treatment was 11 months (1-32 months) and the median starting dose was 50 mg/day (12, 5-75 mg/day). Thirty-two patients (45%) required one or more concomitant ITP medications during the first 6 months of treatment with eltrombopag. Thirty-nine patients (55%) never required concomitant medications. Median platelet counts and proportion of patients achieving the target platelet count of at least 30 × 10/L and 100 × 10/L significantly increased during the first 6 months of treatment ( < 0.0001). Additionally, eltrombopag has been proved effective in the absence of concomitant therapies. The most common Adverse Events were headache (7%) and thrombocytosis (6%). Our study highlighted the crucial role of eltrombopag as second line treatment in children with chronic ITP.
血小板生成素受体激动剂艾曲泊帕已被证明对慢性免疫性血小板减少症(ITP)患儿安全有效。本研究的目的是描述艾曲泊帕在当前临床实践中的使用情况。这是一项在意大利儿科血液学和肿瘤学协会(AIEOP)下属的17个中心进行的回顾性多中心研究。该研究的主要目的是确定在欧洲药品管理局(EMA)批准用于儿科年龄后,意大利慢性ITP患儿中使用艾曲泊帕的患病率。次要目的是评估当前临床实践中艾曲泊帕治疗前6个月的疗效和整个治疗期间 的安全性。共有386例慢性ITP患儿被回顾性纳入并符合分析条件。在这些患者中,71例接受了艾曲泊帕治疗。艾曲泊帕的使用率为19%(95%CI 0.15 - 0.23)。31例患者(44%)为男性,40例患者(56%)为女性。首次服用艾曲泊帕的中位年龄为12岁(3 - 17岁)。艾曲泊帕治疗的中位持续时间为11个月(1 - 32个月),中位起始剂量为50mg/天(12.5 - 75mg/天)。32例患者(45%)在使用艾曲泊帕治疗的前6个月需要一种或多种ITP伴随药物。39例患者(55%)从未需要伴随药物。治疗前6个月期间,血小板计数中位数和达到至少30×10⁹/L和100×10⁹/L目标血小板计数的患者比例显著增加(P < 0.0001)。此外,在没有伴随治疗的情况下,艾曲泊帕也已被证明是有效的。最常见的不良事件是头痛(7%)和血小板增多症(6%)。我们的研究强调了艾曲泊帕作为慢性ITP患儿二线治疗的关键作用。