Suppr超能文献

挽救性治疗移植后淋巴细胞增生性疾病(PTLD)复发且在初始化疗后PTLD出现二次进展的情况:利妥昔单抗单药治疗的作用

Salvage therapy for relapsed posttransplant lymphoproliferative disorders (PTLD) with a second progression of PTLD after Upfront chemotherapy: the role of single-agent rituximab.

作者信息

Trappe Ralf U, Choquet Sylvain, Reinke Petra, Dreyling Martin, Mergenthaler Hans-Günther, Jäger Ulrich, Kebelmann-Betzing Christian, Jonas Sven, Lehmkuhl Hans, Anagnostopoulos Ioannis, Leblond Véronique, Hetzer Roland, Dörken Bernd, Riess Hanno, Oertel Stephan

机构信息

Department of Hematology and Oncology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Berlin, Germany.

出版信息

Transplantation. 2007 Dec 27;84(12):1708-12. doi: 10.1097/01.tp.0000295987.12996.19.

Abstract

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.

摘要

目前,对于免疫抑制降低失败后化疗复发或难治的移植后淋巴细胞增生性疾病患者,尚无标准治疗方法。我们分析了在这种情况下单药利妥昔单抗治疗8例患者(7例成人,1例儿童)的效果。3例患者曾多次接受利妥昔单抗挽救治疗。在7例成人患者中,利妥昔单抗挽救治疗使3例患者(43%)达到完全缓解(CR),1例(14%)达到部分缓解。在儿童患者中,获得了部分缓解,复发时重复使用利妥昔单抗可再次诱导缓解。达到CR的患者要么维持CR状态,要么再次成功接受单药利妥昔单抗挽救治疗。中位随访69个月时,无进展生存期的中位数为9个月,未观察到相关的治疗相关毒性。在这种经过强化预处理的患者中,单药利妥昔单抗挽救治疗是一种有效的治疗选择,几乎没有治疗相关毒性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验