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临床试验/NL-OMON28762
NL-OMON28762尚未招募不适用

Effect of a single dose of 14.8 MBq/kg (0.4 mCi/kg) 90Y-ibritumomab tiuxetan (Zevalin”) following first-line R-CVP therapy in patients with follicular lymphoma on conversion rate assessed by FDG-PET and on stem cell mobilisation. A Phase II clinical trial.

Vumc, hematology department0 个研究点目标入组 31 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
尚未招募
发起方
入组人数
31

研究概览

简要总结

/A

研究设计

研究类型
Interventional

入排标准

入选标准

  • 1. Histologically confirmed (according to WHO classification) CD 20 positive follicular lymphoma, grade 1, 2 or 3a, stage II, III or IV (with indication for treatment following local guidelines) of all FLIPI scores;
  • 2. Age 18 years or older, for stem cell mobilisation analysis age 18-61 years;

排除标准

  • 1. Any other anticancer treatment for NHL except the first line R-CVP;
  • 2. Prolonged cytopenia during first line induction chemotherapy requiring more than 2 weeks delay due to insufficient bone marrow reserve;

研究者

发起方
Vumc, hematology department

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