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肾移植后使用利妥昔单抗治疗移植后淋巴增殖性疾病并转换为m-TOR抑制剂。

Treatment of post-transplantation lymphoproliferative disorders after kidney transplant with rituximab and conversion to m-TOR inhibitor.

作者信息

Nieto-Rios John Fredy, Gómez de Los Ríos Sandra Milena, Serna-Higuita Lina María, Ocampo-Kohn Catalina, Aristizabal-Alzate Arbey, Gálvez-Cárdenas Kenny Mauricio, Zuluaga-Valencia Gustavo Adolfo

机构信息

Sección Nefrología, Hospital Pablo Tobon Uribe, Medellin,Colombia; Universidad de Antioquia, Medellin, Colombia.

Universidad Pontificia Bolivariana, Medellin, Colombia.

出版信息

Colomb Med (Cali). 2016 Dec 30;47(4):196-202.

Abstract

BACKGROUND

Post-transplantation lymphoproliferative disorders are serious complications of organ transplantation which treatment is not yet standardized.

OBJECTIVE

To describe the clinical response, overall and graft survival of patients in our center with this complication after kidney transplantation, which received rituximab as part of their treatment as well as conversion to m-TOR.

METHODS

Retrospective study, which included patients, diagnosed with post-transplant lymphoproliferative disorders after kidney transplantation from January 2011 to July 2014.

RESULTS

Eight cases were found with a wide spectrum of clinical presentations. Most had monomorphic histology, 85% were associated with Epstein-Barr virus, 25% of patients had tumor involvement of the renal graft, and 12.5% ​​had primary central nervous system lymphoma. All patients were managed with reduction of immunosuppression, conversion to m-TOR (except one who lost the graft at diagnosis) and rituximab-based therapy. The overall response rate was 87.5% (62.5% complete response, 25% partial response). Survival was 87.5% with a median follow-up of 34 months. An additional patient lost the graft, with chronic nephropathy already known. All the remaining patients had stable renal function.

CONCLUSIONS

There are no standardized treatment regimens for lymphoproliferative disorders after kidney transplantation, but these patients can be managed successfully with reduction of immunosuppression, conversion to m-TOR and rituximab-based schemes.

摘要

背景

移植后淋巴增殖性疾病是器官移植的严重并发症,其治疗尚未标准化。

目的

描述在我们中心肾移植后发生这种并发症的患者的临床反应、总体生存率和移植物生存率,这些患者接受利妥昔单抗作为其治疗的一部分以及转换为m-TOR治疗。

方法

回顾性研究,纳入2011年1月至2014年7月肾移植后诊断为移植后淋巴增殖性疾病的患者。

结果

发现8例患者,临床表现多样。大多数具有单形性组织学特征,85%与EB病毒相关,25%的患者肾移植有肿瘤累及,12.5%有原发性中枢神经系统淋巴瘤。所有患者均通过减少免疫抑制、转换为m-TOR(诊断时除1例失去移植物者外)和基于利妥昔单抗的治疗进行管理。总体缓解率为87.5%(完全缓解62.5%,部分缓解25%)。中位随访34个月时生存率为87.5%。另有1例患者失去移植物,其已有慢性肾病。其余所有患者肾功能稳定。

结论

肾移植后淋巴增殖性疾病尚无标准化治疗方案,但这些患者通过减少免疫抑制、转换为m-TOR和基于利妥昔单抗的方案可成功治疗。

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