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造血干细胞移植患儿静脉闭塞性疾病/窦性阻塞综合征的回顾性分析——一项多中心研究

Retrospective analysis of veno-occlusive disease/sinusoidal obstruction syndrome in paediatric patients undergoing hematopoietic cell transplantation -a multicentre study.

作者信息

Ragoonanan Dristhi, Abdel-Azim Hisham, Sharma Aditya, Bhar Saleh, McArthur Jennifer, Madden Renee, Rahrig April, Bajwa Rajinder, Wang Jian, Sun Victoria, Wright Mariah, Lassiter Rebekah, Shoberu Basirat, Kawedia Jitesh, Khazal Sajad Jawad, Mahadeo Kris Michael

机构信息

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Division of Transplant and Cell Therapy, Loma Linda University Cancer Center, Loma Linda, CA 92354, USA.

出版信息

Lancet Reg Health Am. 2024 Apr 6;33:100728. doi: 10.1016/j.lana.2024.100728. eCollection 2024 May.

Abstract

BACKGROUND

Sinusoidal obstruction syndrome is a potentially fatal complication following hematopoietic cell transplantation, high-intensity chemotherapies and increasingly seen with calicheamicin based leukemia therapies. Paediatric specific European Society for Blood and Marrow Transplantation (pEBMT) diagnostic criteria have demonstrated benefit in single center studies compared to historic criteria. Yet, the extent to which they have been universally implemented remains unclear.

METHODS

We conducted a retrospective multi-centre study to examine the potential impact of the Baltimore, modified Seattle and pEBMT criteria on the incidence, severity, and outcomes of sinusoidal obstruction syndrome among paediatric hematopoietic cell transplantation patients.

FINDINGS

The incidence of sinusoidal obstruction syndrome in this cohort (n = 488) was higher by pEBMT (21.5%) vs historic modified Seattle (15.6%) and Baltimore (7.0%) criteria (p < 0.001). Application of pEBMT criteria identified 44 patients who were not previously diagnosed with sinusoidal obstruction syndrome. Overall, 70.5% of all patients diagnosed with sinusoidal obstruction syndrome ultimately developed very severe disease and almost half of diagnosed patients required critical care support. Overall survival was significantly lower in patients who were diagnosed with sinusoidal obstruction syndrome vs those who were not.

INTERPRETATION

Taken together, pEBMT criteria may be a sensitive method for prompter diagnosis of patients who subsequently develop severe/very severe sinusoidal obstruction syndrome. To our knowledge, this is the first multi-centre study in the United States (US) to demonstrate that pEBMT guidelines are associated with earlier detection of sinusoidal obstruction syndrome. Since early initiation of definitive treatment for sinusoidal obstruction syndrome has been associated with improved survival in paediatric patients and implementation of pEBMT criteria appears feasible in the US, universal adoption should facilitate prompter diagnosis and lead to improved outcomes of children with sinusoidal obstruction syndrome.

FUNDING

None.

摘要

背景

窦性阻塞综合征是造血细胞移植、高强度化疗后一种潜在的致命并发症,在基于卡奇霉素的白血病治疗中也越来越常见。与传统标准相比,欧洲儿科血液与骨髓移植学会(pEBMT)的特定诊断标准在单中心研究中已显示出优势。然而,这些标准在全球范围内的实施程度仍不明确。

方法

我们进行了一项回顾性多中心研究,以检验巴尔的摩标准、改良西雅图标准和pEBMT标准对儿科造血细胞移植患者窦性阻塞综合征的发病率、严重程度及预后的潜在影响。

研究结果

在该队列(n = 488)中,根据pEBMT标准诊断的窦性阻塞综合征发病率(21.5%)高于传统改良西雅图标准(15.6%)和巴尔的摩标准(7.0%)(p < 0.001)。应用pEBMT标准发现了44例先前未被诊断为窦性阻塞综合征的患者。总体而言,所有被诊断为窦性阻塞综合征的患者中,70.5%最终发展为非常严重的疾病,近一半的确诊患者需要重症监护支持。与未被诊断为窦性阻塞综合征的患者相比,被诊断为该综合征的患者总体生存率显著更低。

解读

综上所述,pEBMT标准可能是一种敏感的方法,可用于更早地诊断随后发展为严重/非常严重窦性阻塞综合征的患者。据我们所知,这是美国第一项多中心研究,证明pEBMT指南与窦性阻塞综合征的早期检测相关。由于窦性阻塞综合征的早期确定性治疗已与儿科患者生存率的提高相关,且pEBMT标准在美国的实施似乎可行,普遍采用应有助于更早诊断,并改善窦性阻塞综合征患儿的预后。

资金来源

无。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa27/11015489/d7f1ae0c2524/gr1.jpg

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