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