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小儿肝移植受者中与 EBV 相关的移植后淋巴增殖性疾病的危险因素。

Epstein-Barr virus-associated risk factors for post-transplant lymphoproliferative disease in pediatric liver transplant recipients.

机构信息

Pediatric Hepatology and Liver Transplant Unit, Vall d'Hebron University Hospital, Barcelona, Spain.

Pediatric Oncology and Hematology Department, Vall d'Hebron University Hospital, Barcelona, Spain.

出版信息

Pediatr Transplant. 2022 Sep;26(6):e14292. doi: 10.1111/petr.14292. Epub 2022 Apr 24.

DOI:10.1111/petr.14292
PMID:35466492
Abstract

BACKGROUND

Post-transplant lymphoproliferative disorder (PTLD) are the most common de novo malignancies after liver transplantation (LT) in children. The aim of our study was to assess the role of pre-LT EBV status and post-LT EBV viral load as risk factors for developing PTLD in a cohort of pediatric LT recipients.

METHODS

Data of all children who underwent LT between January 2002 and December 2019 were collected. Two cohorts were built EBV pre-LT primary infected cohort and EBV post-LT primary infected cohort. Moreover, using the maximal EBV viral load, a ROC curve was constructed to find a cutoff point for the diagnosis of PTLD.

RESULTS

Among the 251 patients included in the study, fifteen PTLD episodes in 14 LT recipients were detected (2 plasmacytic hyperplasia, 10 polymorphic PTLD, 2 monomorphic PTLD, and 1 Classical-Hodgkin's lymphoma). Patients of the EBV post-LT primary infected cohort were 17.1 times more likely to develop a PTLD than patients of the EBV pre-LT primary infected cohort (2.2-133.5). The EBV viral load value to predict PTLD was set at 211 000 UI/mL (93.3% sensitivity and 77.1% specificity; AUC 93.8%; IC 0.89-0.98). In EBV post-LT primary infected cohort, patients with a viral load above 211 000 were 30 times more likely to develop PTLD than patients with a viral load below this value (OR 29.8; 3.7-241.1; p < 0.001).

CONCLUSIONS

The combination of pretransplant EBV serological status with EBV post-transplant viral load could be a powerful tool to stratify the risk of PTLD in pediatric LT patients.

摘要

背景

移植后淋巴组织增生性疾病(PTLD)是儿童肝移植(LT)后最常见的新发恶性肿瘤。我们的研究目的是评估 LT 前 EBV 状态和 LT 后 EBV 病毒载量作为儿童 LT 受者发生 PTLD 的危险因素。

方法

收集了 2002 年 1 月至 2019 年 12 月期间所有接受 LT 的儿童的数据。建立了 EBV 移植前原发性感染队列和 EBV 移植后原发性感染队列。此外,使用 EBV 病毒载量最大值构建了 ROC 曲线,以找到诊断 PTLD 的截断值。

结果

在研究的 251 名患者中,发现 14 名 LT 受者中有 15 例 PTLD 发作(2 例浆细胞增生、10 例多形性 PTLD、2 例单形性 PTLD 和 1 例经典霍奇金淋巴瘤)。与 EBV 移植前原发性感染队列的患者相比, EBV 移植后原发性感染队列的患者发生 PTLD 的可能性高 17.1 倍(2.2-133.5)。预测 PTLD 的 EBV 病毒载量值设定为 211000 UI/mL(93.3%的敏感性和 77.1%的特异性;AUC 93.8%;IC 0.89-0.98)。在 EBV 移植后原发性感染队列中,病毒载量高于 211000 的患者发生 PTLD 的可能性是病毒载量低于该值的患者的 30 倍(OR 29.8;3.7-241.1;p<0.001)。

结论

LT 前 EBV 血清学状态与 LT 后 EBV 病毒载量的结合可能是 LT 后儿童 PTLD 风险分层的有力工具。

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