首页> 外文期刊>Pediatric blood & cancer >Fludarabine, cyclophosphamide, doxorubicin (FCD), and rituximab: a remission induction therapy for aggressive pediatric post-transplant lymphoproliferative disease (PTLD).
【24h】

Fludarabine, cyclophosphamide, doxorubicin (FCD), and rituximab: a remission induction therapy for aggressive pediatric post-transplant lymphoproliferative disease (PTLD).

机译:氟达拉滨,环磷酰胺,阿霉素(FCD)和利妥昔单抗:缓解性诱导疗法,用于小儿移植后侵袭性增生性疾病(PTLD)。

获取原文
获取原文并翻译 | 示例
       

摘要

Management of aggressive, usually late-occurring, post-transplant lymphoproliferative disorders (PTLDs), a life-threatening complication after solid organ transplants, remains controversial. Four children affected by aggressive CD20+ PTLDs received a chemo-immunotherapy regimen for remission induction based on fludarabine, cyclophosphamide, doxorubicin, and rituximab, associated with a rapid discontinuation of immunosuppression (IS). Subsequent consolidation chemotherapy consisted of Berlin-Frankfurt-Munster-modified blocks. All patients achieved a complete remission, which persisted for 25, 68+, 80+, and 103+ months after diagnosis. Therapy was well tolerated. No patients developed allograft rejection during PTLD treatment. Our experience suggests that this chemo-immunotherapeutic approach may be an effective treatment strategy while allowing for a concomitant discontinuation of IS.
机译:侵袭性,通常为晚期发生的移植后淋巴组织增生性疾病(PTLD)的管理仍存在争议,这是实体器官移植后危及生命的并发症。受侵袭性CD20 + PTLD影响的四名儿童接受了基于氟达拉滨,环磷酰胺,阿霉素和利妥昔单抗的化学免疫疗法诱导缓解,并伴有免疫抑制剂(IS)的快速停用。随后的巩固化疗包括柏林-法兰克福-芒斯特修饰的嵌段。所有患者均实现了完全缓解,诊断后持续了25、68 +,80 +和103+个月。治疗耐受性好。在PTLD治疗期间,没有患者出现同种异体移植排斥反应。我们的经验表明,这种化学免疫治疗方法可能是一种有效的治疗策略,同时允许同时终止IS。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号