跳至主要内容
临床试验/NL-OMON48552
NL-OMON48552已完成不适用

Response assessment of post-transplant lymphoproliferative disorder with 18F-FDG-PET/CT and minimal residual disease monitoring, a multicenter multinational feasibility study - Minimal residual disease monitoring in PTLD

niversitair Medisch Centrum Groningen0 个研究点目标入组 30 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Patients having undergone a solid organ transplantation or hematopoietic stem
  • cell transplantation.
  • - Histologically proven CD20+ monomorphic PTLD (with or without EBV association)
  • - Age > 18 years
  • - Intent to treat patient according to standard protocol (rituximab / R-CHOP).
  • Clinicians are allowed to adapt protocol in the best interest of the patient
  • - Measurable disease on 18F-FDG-PET/CT at diagnosis
  • -Patient*s written informed consent and written consent for data collection.

排除标准

  • -A complete surgical resection of tumor.
  • -Upfront treatment with external beam radiation therapy.
  • -Known to be HIV positive.

研究者

相似试验