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临床试验/EUCTR2007-005920-34-NL
EUCTR2007-005920-34-NL进行中(未招募)不适用

HD17 for Intermediate Stage Hodgkin Lymphoma - Treatment Optimization Trial in the First-Line Treatment of intermediate Stage Hodgkin lymhoma; Therapy stratification by means of FDG-PET - HD17

VU University Medical Center0 个研究点目标入组 1,100 人开始时间: 2012年8月16日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
1,100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Histologically proven Hodgkin lymphoma
  • Newly diagnosed, no previous treatment
  • Stage I, IIA with RF a-d; stage IIB with RF c, d
  • (a: large mediastinal mass, b: extranodal disease, c: high ESR, d: = 3 lymph node areas)
  • Age: 18-60 years
  • Patient had no previous treatment for HL
  • Normal organ function (except HL-related);
  • Life expectancy > 3 months.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 30
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Composite lymphoma
  • Previous malignancy, prior chemotherapy or radiotherapy
  • Concurrent diseases which preclude protocol treatment
  • Pregnancy, lactation
  • Non-compliance
  • WHO activity index > 2
  • Antiepileptic treatment
  • Concurrent diseases which preclude protocol treatment
  • Long-term administration of corticosteroids (e.g. for chronic polyarthritis) or antineoplastic drugs (e.g. azathioprine, methotrexate)

研究者

发起方
VU University Medical Center

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