Monitoring and Management of Cytomegalovirus Reactivations After Allogeneic Hematopoietic Stem Cell Transplantation in Children: Experience from a Single Pediatric Center.

IF 3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL Diagnostics Pub Date : 2024-11-03 DOI:10.3390/diagnostics14212461
Giulia Ferrando, Francesca Bagnasco, Stefano Giardino, Filomena Pierri, Sara Pestarino, Eddi Di Marco, Maria Santaniello, Elio Castagnola, Maura Faraci
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Abstract

Background: CMV reactivation represents a frequent complication after HSCT. The aim of this study was to describe the incidence of CMV reactivation in a pediatric HSCT cohort and analyze the potential impact of recipient/donor-related or transplant-related factors on this complication. Furthermore, we analyzed the management of CMV reactivation in order to purpose criteria for pre-emptive therapy.

Methods: Allogeneic HSCTs, performed at IRCCS Istituto Gaslini between 2012 and 2022, were included in this analysis. CMV-DNAemia was regularly monitored. Risk stratification was based on donor/recipient serological status and additional potential risk factors were considered: haploidentical transplant; any HSCT subsequent to the first; acute and chronic GvHD; steroids; and other immunosuppressive therapies. We described also the approach for pre-emptive therapy during the period 2012-2019.

Results: A total of 214 allogeneic HSCTs were performed in 189 patients. In total, 100 (46.7%) HSCTs were complicated by at least one reactivation. CMV reactivation was significantly associated with high serological risk and steroid treatment. Pre-emptive therapy was administered in 59/69 (85.5%) HSCTs during 2012-2019. In the presence of predefined risk conditions, therapy was started at a median viremia of 2050 copies/mL. No difference was observed in OS between patients with CMV reactivation versus patients who did not present this complication.

Conclusions: These results suggest the potential effectiveness of the approach used in providing pre-emptive therapy based on viral load monitoring and individualized risk factors.

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儿童异基因造血干细胞移植后巨细胞病毒再激活的监测和管理:单个儿科中心的经验。
背景:CMV 再激活是造血干细胞移植后的常见并发症:CMV再激活是造血干细胞移植后的一种常见并发症。本研究旨在描述儿科造血干细胞移植队列中 CMV 再激活的发生率,并分析受者/供者相关因素或移植相关因素对这一并发症的潜在影响。此外,我们还分析了CMV再激活的处理方法,以制定先期治疗的标准:分析对象包括 2012 年至 2022 年期间在 IRCCS Istituto Gaslini 进行的异基因造血干细胞移植。定期监测CMV-DNA血症。根据供体/受体血清学状态进行风险分层,并考虑其他潜在风险因素:单倍体移植;第一次造血干细胞移植后的任何造血干细胞移植;急性和慢性GvHD;类固醇;以及其他免疫抑制疗法。我们还介绍了2012-2019年期间的先期治疗方法:189名患者共接受了214例异体造血干细胞移植。共有 100 例(46.7%)造血干细胞移植因至少一次再激活而变得复杂。CMV再激活与高血清学风险和类固醇治疗密切相关。2012-2019年期间,59/69例(85.5%)造血干细胞移植患者接受了预防性治疗。如果存在预定义的风险条件,则在病毒血症中位数为2050拷贝/毫升时开始治疗。在OS方面,未观察到CMV再激活患者与未出现该并发症患者之间的差异:这些结果表明,根据病毒载量监测和个体化风险因素提供先期治疗的方法具有潜在的有效性。
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来源期刊
Diagnostics
Diagnostics Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
4.70
自引率
8.30%
发文量
2699
审稿时长
19.64 days
期刊介绍: Diagnostics (ISSN 2075-4418) is an international scholarly open access journal on medical diagnostics. It publishes original research articles, reviews, communications and short notes on the research and development of medical diagnostics. There is no restriction on the length of the papers. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible. Full experimental and/or methodological details must be provided for research articles.
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