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代表 EBMT 的先天错误、传染病和儿科疾病工作组,对儿科异基因 HSCT 项目中的 CMV 管理进行调查。

Survey of CMV management in pediatric allogeneic HSCT programs, on behalf of the inborn errors, infectious diseases and pediatric diseases working parties of EBMT.

机构信息

Department of Hematology and Immunology, Hospital Robert Debre, Paris 7-Paris Diderot University, Paris, France.

Department of Pediatric Hematology and Oncology, University Hospital Motol, 2nd Medical School, Charles University, Prague, Czech Republic.

出版信息

Bone Marrow Transplant. 2014 Feb;49(2):276-9. doi: 10.1038/bmt.2013.164. Epub 2013 Oct 28.

Abstract

Human CMV infection is a frequent complication after HSC in children with remarkable morbidity and mortality. Antiviral drugs are relatively efficient but have numerous side effects. They are used as prophylactic, pre-emptive or therapeutic medicines. It is still a matter of debate which option is the best strategy. No uniform procedure has emerged regarding these three options, and new immunologic tools have raised more questions for physicians. To assess the current practice in the management of CMV infection, we sent a questionnaire to the EBMT centers performing hematopoietic SCT (HSCT) in children. Fifty-six out of 196 responded to the questionnaire (28.5%). Quantitative PCR was the most common monitoring tool (44/56). Only 4/56 centers use the pp65 antigenemia alone. All centers used pre-emptive strategy (56/56). 21/56 centers also used prophylactic measures, 13/21 after analysis of donor/receptor serologic status. Ganciclovir was the most common first-line agent for CMV disease (55/56). The most common dose and duration for induction treatment were 5 mg/kg bid (47/55) for 14 days (20/55). There is no uniform procedure for researching resistance strain, antiviral second-line therapy or cell therapy. A harmonization process should enable sound prospective trials to improve prevention, control and cure of CMV disease in children and adolescents.

摘要

人类巨细胞病毒(CMV)感染是儿童造血干细胞移植(HSC)后的常见并发症,具有显著的发病率和死亡率。抗病毒药物虽然相对有效,但有许多副作用,被用作预防、先发制人和治疗药物。哪种选择是最佳策略仍存在争议。对于这三种选择,尚未出现统一的程序,新的免疫工具也给医生带来了更多的问题。为了评估目前在 CMV 感染管理方面的实际情况,我们向进行儿童造血干细胞移植(HSCT)的 EBMT 中心发送了一份问卷。196 个中心中有 56 个(28.5%)做出了回应。定量聚合酶链反应(PCR)是最常见的监测工具(44/56)。只有 4/56 的中心单独使用 pp65 抗原血症。所有中心均采用先发制人的策略(56/56)。21/56 个中心还采取了预防措施,其中 13/21 是根据供体/受体血清学状况进行分析的。更昔洛韦是治疗 CMV 疾病的最常用一线药物(55/56)。诱导治疗最常用的剂量和持续时间为 5mg/kg bid(47/55),持续 14 天(20/55)。对于耐药株的研究、抗病毒二线治疗或细胞治疗,目前尚无统一的程序。一个协调的过程应该能够进行合理的前瞻性试验,以改善儿童和青少年 CMV 疾病的预防、控制和治疗。

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