González-López Tomás José, Alvarez-Román María Teresa, Pascual Cristina, Sánchez-González Blanca, Fernández-Fuentes Fernando, Jarque Isidro, Pérez-Rus Gloria, Pérez-Crespo Susana, Bernat Silvia, Hernández-Rivas José Angel, Andrade Marcio M, Cortés Montserrat, Gómez-Nuñez Marta, Olivera Pavel, Martínez-Robles Violeta, Fernández-Rodríguez Angeles, Fuertes-Palacio Miguel Angel, Fernández-Miñano Carmen, de Cabo Erik, Fisac Rosa, Aguilar Carlos, Bárez Abelardo, Peñarrubia María Jesús, García-Frade Luis Javier, González-Porras José Ramón
Department of Hematology, Hospital Universitario de Burgos, Burgos, Spain.
Department of Hematology, Hospital Universitario La Paz, Madrid, Spain.
Eur J Haematol. 2016 Sep;97(3):297-302. doi: 10.1111/ejh.12725. Epub 2016 Jan 27.
Eltrombopag is effective and safe in chronic immune thrombocytopenia (ITP). However, clinical trials may not accurately reflect what happens in clinical practice. We evaluated the efficacy and safety of eltrombopag in primary chronic ITP in a real-world setting.
A total of 164 primary patients with chronic ITP from 40 Spanish centers, who had been treated with eltrombopag, were retrospectively evaluated.
The median age of our cohort (72% women) was 63 yr (interquartile range, IQR, 45-75 yr). The median time with ITP diagnosis was 81 months (IQR, 30-192 months). The median number of therapies prior to eltrombopag was 3 (IQR, 2-4). At the time of eltrombopag start, 45 patients (30%) were receiving concomitant treatment for ITP. Forty-six patients (30%) had bleeding signs/symptoms the month before the treatment started. The median platelet count at eltrombopag initiation was 22 × 10(9) /L (IQR, 8-39 × 10(9) /L). A total of 135 patients (88.8%) achieved a platelet response. The median time to platelet response was 12 d (95% CI, 9-13 d). Maintained platelet response rate during the 15-month period under examination was 75.2%. Twenty-eight patients (18.4%) experienced adverse events, mainly grades 1-2.
Eltrombopag is highly effective and well tolerated in unselected patients with primary chronic ITP.
艾曲泊帕在慢性免疫性血小板减少症(ITP)中有效且安全。然而,临床试验可能无法准确反映临床实践中的情况。我们评估了艾曲泊帕在真实世界中治疗原发性慢性ITP的疗效和安全性。
回顾性评估了来自西班牙40个中心的164例接受过艾曲泊帕治疗的原发性慢性ITP患者。
我们队列的中位年龄为63岁(四分位间距,IQR,45 - 75岁),其中女性占72%。ITP诊断后的中位时间为81个月(IQR,30 - 192个月)。在开始使用艾曲泊帕之前,治疗的中位次数为3次(IQR,2 - 4次)。开始使用艾曲泊帕时,45例患者(30%)正在接受ITP的联合治疗。46例患者(30%)在治疗开始前一个月有出血体征/症状。开始使用艾曲泊帕时的中位血小板计数为22×10⁹/L(IQR,8 - 39×10⁹/L)。共有135例患者(88.8%)获得了血小板反应。达到血小板反应的中位时间为12天(95%CI,9 - 13天)。在检查的15个月期间,维持血小板反应率为75.2%。28例患者(18.4%)发生不良事件,主要为1 - 2级。
艾曲泊帕在未经选择的原发性慢性ITP患者中高效且耐受性良好。