Department of Haematology, Oncology, and Stem Cell Transplantation, University of Regensburg, Franz-Josef-Strauß-Allee 11, 93053, Regensburg, Germany.
NOVEL Health Strategies, Bethesda, MD, USA.
Clin Drug Investig. 2022 Jun;42(6):465-476. doi: 10.1007/s40261-022-01140-y. Epub 2022 May 20.
Defibrotide is approved to treat severe veno-occlusive disease/sinusoidal obstruction syndrome (VOD/SOS) after haematopoietic cell transplantation in patients aged > 1 month in the European Union and for VOD/SOS with renal/pulmonary dysfunction post-haematopoietic cell transplantation in the United States. This meta-analysis estimated the incidence and risk of VOD/SOS after intravenous defibrotide prophylaxis using the published literature.
PubMed, Embase and Web of Science were searched through 30 November 2021 for defibrotide studies in VOD/SOS "prevention" or "prophylaxis," excluding phase I studies, case reports, studies with fewer than ten patients and reviews.
The search identified 733 records; 24 met inclusion criteria, of which 20 (N = 3005) evaluated intravenous defibrotide for VOD/SOS prophylaxis. Overall VOD/SOS incidence with intravenous defibrotide was 5%, with incidences of 5% in adults and 8% in paediatric patients. In eight studies with data on intravenous defibrotide prophylaxis vs controls (e.g. heparin, no prophylaxis), VOD/SOS incidence in controls was 16%. The risk ratio for developing VOD/SOS with defibrotide prophylaxis vs controls was 0.30 (95% confidence interval 0.12-0.71; p = 0.006).
This analysis suggests a low incidence of VOD/SOS following intravenous defibrotide prophylaxis, regardless of age group, and a lower relative risk for VOD/SOS with defibrotide prophylaxis vs controls in patient populations at high risk of VOD/SOS.
在欧盟,对于年龄>1 个月的造血细胞移植患者,批准使用去纤维肽治疗造血细胞移植后严重的静脉阻塞性疾病/窦阻塞综合征(VOD/SOS);在美国,批准用于造血细胞移植后伴有肾/肺功能障碍的 VOD/SOS。本荟萃分析旨在根据已发表的文献评估静脉注射去纤维肽预防 VOD/SOS 的发生率和风险。
通过 PubMed、Embase 和 Web of Science,检索了截至 2021 年 11 月 30 日的去纤维肽预防 VOD/SOS 的研究,检索词包括“预防”或“预防”,排除了 I 期研究、病例报告、患者少于 10 例的研究和综述。
共检索到 733 条记录,其中 24 条符合纳入标准,其中 20 条(N=3005)评估了静脉注射去纤维肽预防 VOD/SOS。静脉注射去纤维肽预防 VOD/SOS 的总体发生率为 5%,其中成人和儿科患者的发生率分别为 5%和 8%。在 8 项研究中,静脉注射去纤维肽预防组与对照组(如肝素、无预防)的数据显示,对照组的 VOD/SOS 发生率为 16%。与对照组相比,去纤维肽预防组发生 VOD/SOS 的风险比为 0.30(95%置信区间 0.12-0.71;p=0.006)。
无论年龄组如何,静脉注射去纤维肽预防后 VOD/SOS 的发生率均较低,在 VOD/SOS 高危患者中,与对照组相比,去纤维肽预防组 VOD/SOS 的相对风险较低。