首页> 外文期刊>Transplant international : >Anti-CD20 monoclonal antibody treatment of Epstein-Barr virus-induced intrahepatic lymphoproliferative disorder following liver transplantation.
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Anti-CD20 monoclonal antibody treatment of Epstein-Barr virus-induced intrahepatic lymphoproliferative disorder following liver transplantation.

机译:肝移植后抗CD20单克隆抗体治疗爱泼斯坦-巴尔病毒引起的肝内淋巴增生性疾病。

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Epstein-Barr virus (EBV)-associated post-transplant lymphoproliferative disorders (PTLDs) are a common cause of death in transplant patients. Their incidence following liver transplantation is reported to be between 0.5% and 4%. Despite various therapeutic approaches, there is still no consensus on a treatment strategy. The treatment of transplant recipients with monoclonal antibodies directed against B-cell antigens is a new, therapeutic approach with which, however, little clinical experience has so far been gained. Two patients developed intrahepatic PTLD 7 and 15 months, respectively, after transplantation. In one case, this was diagnosed as polymorphic PTLD, in the other as monomorphic, monoclonal PTLD. After having their immunosuppression terminated, 4 weeks after establishment of the diagnosis, both patients were treated with anti-CD20 antibodies (rituximab) at a dose of 375 mg/m(2) on days 1, 8, 15 and 22. Treatment with rituximab was tolerated well by both patients. One of the patients in whomcholestasis parameters remained high underwent re-transplantation. In one of the cases, the histological work-up confirmed necrosis of 90% of the tumour cells, and complete remission in the other. Both patients died of secondary complications 10 weeks and 10 months, respectively, after the diagnosis of PTLD. We can conclude that treatment of PTLD with Rituximab led to remission in both of our patients. Nevertheless, progression of cholestasis persisted, and both patients ultimately died of complications unrelated to PTLD.
机译:与爱泼斯坦巴尔病毒(EBV)相关的移植后淋巴组织增生性疾病(PTLDs)是移植患者死亡的常见原因。据报道,它们在肝移植后的发生率在0.5%至4%之间。尽管有各种治疗方法,但在治疗策略上仍未达成共识。用针对B细胞抗原的单克隆抗体对移植受体进行治疗是一种新的治疗方法,但是迄今为止,获得的临床经验很少。两名患者分别在移植后7个月和15个月出现肝内PTLD。在一个案例中,这被诊断为多态PTLD,在另一案例中被诊断为单态,单克隆PTLD。在确定诊断后4周,终止免疫抑制后,在第1、8、15和22天用375 mg / m(2)的抗CD20抗体(利妥昔单抗)治疗了这两名患者。两位患者对它的耐受性都很好。胆汁淤积参数仍然很高的一名患者接受了再移植。在一种情况下,组织学检查证实了90%的肿瘤细胞坏死,而另一种则完全缓解。两名患者分别在PTLD诊断后10周和10个月死亡。我们可以得出结论,利妥昔单抗对PTLD的治疗导致我们两个患者的缓解。然而,胆汁淤积的进展持续存在,并且两名患者最终都死于与PTLD无关的并发症。

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