Epstein–Barr Virus-Associated Smooth Muscle Tumor After Kidney Transplantation: A French Multicenter Retrospective Study

IF 1.9 4区 医学 Q2 SURGERY Clinical Transplantation Pub Date : 2024-08-13 DOI:10.1111/ctr.15424
Laurène Tardieu, Dany Anglicheau, Rebecca Sberro-Soussan, Mathilde Lemoine, Léonard Golbin, Ophélie Fourdinier, Julie Bruneau, Marina Charbit, Tchao Meatchi, Jean-Emmanuel Serre, Moglie Le Quintrec, Alexandre Karras, Eric Thervet, Hélène Lazareth
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Abstract

Background

Epstein–Barr virus (EBV) is a herpesvirus linked to nine different human tumors and lymphoproliferative disorders. Immunosuppression promotes EBV-driven malignancies. The most frequent EBV-induced malignancies are lymphomas and nasopharyngeal carcinoma. By promoting smooth muscle proliferation, EBV can induce EBV-associated smooth muscle tumors (EBV-SMT). EBV-SMT is a rare oncological entity for which no current guideline for diagnosis or management exists. Data on posttransplant EBV-SMT (PT-SMT) are scarce in kidney transplant recipients.

Methods

We conducted a national multicentric retrospective study and collected cases among transplantation centers in France. Kidney transplant recipients experiencing histologically proven PT-SMT were included. We collected data on demographic characteristics of patient, history of kidney transplantation, history of PT-SMT, evolution of graft function, and patient survival.

Results

Eight patients were included. The median age at PT-SMT diagnosis was 31 years (range 6.5–40). PT-SMT occurred after a median delay of 37.8 months after transplantation (range 6–175). PT-SMT management consisted in immunosuppressive regimen minimization in all patients. Introduction of mTOR inhibitors was performed in two patients. Four patients (50%) needed chemotherapy. Surgical resection was performed in four patients. At last follow-up after PT-SMT diagnosis (median 33 months (range 17–132)), five patients were considered in complete remission, and two patients had died. Two patients experienced graft rejection; two resumed dialysis (25%). All patients with available data presented with impaired graft function at last follow-up.

Conclusion

PT-SMT is a subacute and progressive disease during kidney transplantation. Even if the risk of developing PT-SMT is low in kidney transplant recipients (0.07% in our cohort), PT-SMT is associated with significant graft loss, possibly due to reduced immunosuppression. Developing guidelines could help transplantation teams better manage these patients.

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肾移植后 Epstein-Barr 病毒相关平滑肌瘤:一项法国多中心回顾性研究。
背景:爱泼斯坦-巴氏病毒(EBV)是一种疱疹病毒,与九种不同的人类肿瘤和淋巴增生性疾病有关。免疫抑制会诱发 EBV 导致的恶性肿瘤。最常见的由 EBV 引起的恶性肿瘤是淋巴瘤和鼻咽癌。通过促进平滑肌增殖,EBV 可诱发 EBV 相关平滑肌瘤(EBV-SMT)。EBV-SMT 是一种罕见的肿瘤,目前尚无诊断或治疗指南。有关肾移植受者移植后 EBV-SMT (PT-SMT)的数据很少:我们开展了一项全国性多中心回顾性研究,收集了法国各移植中心的病例。方法:我们开展了一项全国性多中心回顾性研究,收集了法国各移植中心的病例,其中包括经组织学证实患有 PT-SMT 的肾移植受者。我们收集了患者的人口统计学特征、肾移植史、PT-SMT病史、移植物功能演变和患者存活率等数据:结果:共纳入 8 例患者。确诊 PT-SMT 时的中位年龄为 31 岁(6.5-40 岁)。PT-SMT发生的中位延迟时间为移植后37.8个月(6-175个月)。PT-SMT的治疗包括尽量减少所有患者的免疫抑制方案。两名患者使用了 mTOR 抑制剂。四名患者(50%)需要接受化疗。四名患者接受了手术切除。在 PT-SMT 确诊后的最后一次随访中(中位 33 个月(17-132)),有五名患者被认为病情完全缓解,两名患者死亡。两名患者出现了移植排斥反应;两名患者恢复了透析(25%)。所有提供数据的患者在最后一次随访时均出现移植物功能受损:结论:PT-SMT 是肾移植过程中的一种亚急性进展性疾病。即使肾移植受者患 PT-SMT 的风险很低(在我们的队列中为 0.07%),PT-SMT 仍与移植物的重大损失有关,这可能是由于免疫抑制的降低所致。制定指南有助于移植团队更好地管理这些患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Transplantation
Clinical Transplantation 医学-外科
CiteScore
3.70
自引率
4.80%
发文量
286
审稿时长
2 months
期刊介绍: Clinical Transplantation: The Journal of Clinical and Translational Research aims to serve as a channel of rapid communication for all those involved in the care of patients who require, or have had, organ or tissue transplants, including: kidney, intestine, liver, pancreas, islets, heart, heart valves, lung, bone marrow, cornea, skin, bone, and cartilage, viable or stored. Published monthly, Clinical Transplantation’s scope is focused on the complete spectrum of present transplant therapies, as well as also those that are experimental or may become possible in future. Topics include: Immunology and immunosuppression; Patient preparation; Social, ethical, and psychological issues; Complications, short- and long-term results; Artificial organs; Donation and preservation of organ and tissue; Translational studies; Advances in tissue typing; Updates on transplant pathology;. Clinical and translational studies are particularly welcome, as well as focused reviews. Full-length papers and short communications are invited. Clinical reviews are encouraged, as well as seminal papers in basic science which might lead to immediate clinical application. Prominence is regularly given to the results of cooperative surveys conducted by the organ and tissue transplant registries. Clinical Transplantation: The Journal of Clinical and Translational Research is essential reading for clinicians and researchers in the diverse field of transplantation: surgeons; clinical immunologists; cryobiologists; hematologists; gastroenterologists; hepatologists; pulmonologists; nephrologists; cardiologists; and endocrinologists. It will also be of interest to sociologists, psychologists, research workers, and to all health professionals whose combined efforts will improve the prognosis of transplant recipients.
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