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临床试验/ISRCTN23628366
ISRCTN23628366已完成未知

Phase III Trial comparing CHOP to PmitCEBO in Good Risk patients with Histologically Aggressive Non-Hodgkin's Lymphoma

British National Lymphoma Investigation (BNLI) (UK)0 个研究点目标入组 0 人开始时间: 2002年8月19日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方

研究概览

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Previously untreated non-Hodgkin's Lymphoma of the following types: follicular large cell lymphoma, diffuse mixed cell lymphoma diffuse large cell lymphoma diffuse immunoblastic lymphoma 0r Revised European/American Lymphoma (REAL) classification: diffuse large B peripheral T cell lymphoma
  • 2. Bulky stage IA and stages IB-IV (Ann Arbour staging system)
  • 3. Age 18-59 years
  • 4. Measurable or evaluable disease
  • 5. Good prognosis, defined as the presence of no more than one of the following adverse features: Stage III/IV Lactic dehydrogenase (LDH) >upper limit of normal Performance status 2-4 (Eastern Cooperative Oncology Group [ECOG]-World Health Organisation [WHO]) Adequate bone marrow function, indicated by Haemoglobin =10 g/dL Neutrophils =2 x 10^9/L Platelets =100 x 10^9/L
  • 6. Written informed consent

排除标准

  • Does not meet inclusion criteria

研究者

发起方
British National Lymphoma Investigation (BNLI) (UK)

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