首页> 外文期刊>Transplantation: Official Journal of the Transplantation Society >Salvage therapy for relapsed posttransplant lymphoproliferative disorders (PTLD) with a second progression of PTLD after Upfront chemotherapy: the role of single-agent rituximab.
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Salvage therapy for relapsed posttransplant lymphoproliferative disorders (PTLD) with a second progression of PTLD after Upfront chemotherapy: the role of single-agent rituximab.

机译:前期化疗后复发性移植后淋巴组织增生性疾病(PTLD)的抢救疗法:PTLD的第二次进展:单药利妥昔单抗的作用。

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摘要

Currently no standard treatment exists for patients with posttransplant lymphoproliferative disorders relapsed or refractory to chemotherapy after failure of reduction in immunosuppression. We have analyzed the effects of single-agent rituximab treatment in eight patients (seven adult, one pediatric) in this setting. Three patients had been salvaged with rituximab several times. In the seven adults, rituximab salvage therapy achieved complete remission (CR) in three patients (43%) and partial remission in one (14%). In the pediatric patient, a PR was obtained that could be reinduced on relapse with repeated administrations of rituximab. Patients achieving CR either remained in CR or were successfully salvaged again with single-agent rituximab. At a median follow-up of 69 months, median progression-free survival was 9 months and no relevant therapy-associated toxicity was observed. Single-agent rituximab salvage therapy is an effective treatment option in this setting of intensively pretreated patients,with virtually no therapy-associated toxicity.
机译:目前尚无针对免疫抑制降低失败后复发或对化疗难治的移植后淋巴增生性疾病患者的标准治疗方法。我们分析了在这种情况下单药利妥昔单抗治疗对八名患者(七名成人,一名小儿)的影响。 3名患者多次接受利妥昔单抗治疗。在7名成人中,利妥昔单抗挽救疗法在3例患者中实现了完全缓解(CR)(43%),在1例患者中实现了部分缓解(14%)。在儿科患者中,获得的PR可以通过重复施用利妥昔单抗在复发时被还原。达到CR的患者要么留在CR中,要么再次用利妥昔单抗单药成功挽救。中位随访期为69个月,中位无进展生存期为9个月,未观察到与治疗相关的相关毒性。在这种经过大量预处理的患者中,单药利妥昔单抗挽救疗法是一种有效的治疗选择,几乎没有与治疗相关的毒性。

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