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去纤维肽在造血干细胞移植中的应用:西班牙造血干细胞移植组(GETH)的一项多中心调查研究。

Defibrotide in hematopoietic stem cell transplantation: A multicenter survey study of the Spanish Hematopoietic Stem Cell Transplantation Group (GETH).

机构信息

BMT Unit, Hospital Niño Jesús, Madrid, Spain.

BMT Unit, Hospital Vall de Hebrón, Barcelona, Spain.

出版信息

Eur J Haematol. 2021 Jun;106(6):842-850. doi: 10.1111/ejh.13618. Epub 2021 Mar 30.

Abstract

BACKGROUND

Defibrotide is approved in European Union for the treatment of severe sinusoidal obstruction syndrome (SOS) after HSCT. However, it has also been used for SOS prophylaxis, moderate SOS and in other complications such as transplant-associated thrombotic microangiopathy (TAM). The objective of this study was to evaluate current uses, effectiveness and safety of defibrotide in patients with HSCT.

METHODS

This multicenter, retrospective study included patients treated with defibrotide for any indication at 28 HSCT centers of the Grupo Español de Trasplante Hematopoyetico (GETH) including the pediatric subgroup Grupo Español de Trasplante de Medula en Niños (GETMON).

RESULTS

Three hundred and eighty eight patients treated with defibrotide between January 2011 and December 2018 were included. 253 patients were children, and 135 patients were adults. In total, 332 transplants were allogeneic, and the remainder were autologous. Main indications for defibrotide use were severe/very severe SOS in 173 patients, SOS prophylaxis in 135 patients, moderate SOS in 41 patients, TAM in six patients and suspected SOS in 33 patients. Overall survival (OS) at day +100 in the SOS prophylaxis group was 89% (95% CI, 87%-91%). In the group of patients with moderate and severe/very severe SOS, the OS at day +100 was 80% (95% CI, 74%-86%) and 62% (95% CI, 59%-65%), respectively (P = .0015). With a longer follow-up, median of 2 years (4 months-7 years), OS was 63% (95% CI, 59%-67%) in the SOS prophylaxis patients. OS for patients with moderate and severe/very severe SOS groups was 53% (95% CI, 47%-61%) and 26% (95% CI, 22%-30%), respectively (P = .006). 191 patients died, and SOS was the main cause of death in 23 patients (12%).

CONCLUSIONS

Defibrotide has an acceptable safety profile with an improved response in severe/very severe SOS compared with historical controls, mainly in pediatric patients. Use of defibrotide for prophylaxis may improve prognosis of patients at high risk of complications due to endothelial damage such as those who receive a second transplant. SOS has an important impact on the HSCT long-term survival, as can be concluded from our study.

摘要

背景

在欧洲联盟,地西他滨被批准用于治疗造血干细胞移植(HSCT)后的严重窦状隙阻塞综合征(SOS)。然而,它也被用于 SOS 预防、中度 SOS 和其他并发症,如移植相关血栓性微血管病(TAM)。本研究的目的是评估地西他滨在 HSCT 患者中的当前用途、疗效和安全性。

方法

这是一项多中心回顾性研究,纳入了 28 个西班牙造血干细胞移植组(GETH)中心(包括儿科亚组西班牙儿童骨髓移植组(GETMON))治疗的任何适应症使用地西他滨的患者。

结果

2011 年 1 月至 2018 年 12 月期间,共纳入 388 例使用地西他滨的患者。253 例为儿童,135 例为成人。共进行了 332 例异基因移植,其余为自体移植。使用地西他滨的主要适应证为 173 例严重/非常严重 SOS、135 例 SOS 预防、41 例中度 SOS、6 例 TAM 和 33 例疑似 SOS。SOS 预防组第 +100 天的总体生存率(OS)为 89%(95%CI,87%-91%)。在中度和严重/非常严重 SOS 组的患者中,第 +100 天的 OS 分别为 80%(95%CI,74%-86%)和 62%(95%CI,59%-65%)(P=.0015)。随着更长时间的随访,中位随访时间为 2 年(4 个月至 7 年),SOS 预防患者的 OS 为 63%(95%CI,59%-67%)。中度和严重/非常严重 SOS 组患者的 OS 分别为 53%(95%CI,47%-61%)和 26%(95%CI,22%-30%)(P=.006)。191 例患者死亡,SOS 是 23 例患者(12%)死亡的主要原因。

结论

地西他滨具有可接受的安全性,与历史对照相比,严重/非常严重 SOS 的反应有所改善,主要在儿科患者中。对于内皮损伤风险较高(如接受第二次移植)的患者,使用地西他滨预防可能会改善患者的预后。从我们的研究中可以得出结论,SOS 对 HSCT 的长期生存有重要影响。

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