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临床试验/EUCTR2004-003075-37-FI
EUCTR2004-003075-37-FI进行中(未招募)不适用

CHOEP-14 + rituximab with CNS prophylaxis in patients less than 65 years with Diffuse Large B-Cell Lymphoma/Follicular Lymphoma grade III, stage II-IV with risk factors (age adjusted IPI) = 2.A phase II study (NLG-LBC-04)

ordic Lymphoma Group0 个研究点目标入组 150 人开始时间: 2004年9月28日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
150

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

  • 1. Age = 18 - < 65 years.
  • 2. Histology verified according to the WHO classification and with CD20 positivity
  • -Diffuse large B-cell lymphomas with subgroups
  • -Follicular lymphomas grade III
  • 3. Patients in at least stage II with age adjusted IPI score of 2 or 3:
  • Stage III /IV and elevated LDH and/or WHO performance status 2 - 3
  • Stage II and elevated LDH and WHO performance status 2 - 3.
  • 4. Previously untreated.
  • 5. Performance status < 4 (Appendix 2).
  • 6. Written informed consent
  • 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
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Severe cardiac disease (i.e. heart failure, Cardiac function grade III - IV or Left Ventricular Ejection Fraction (LVEF) < 45%.
  • 2. Impaired liver, renal or other organ function not caused by lymphoma and which will interfere with the treatment schedule.
  • 3. Pregnancy.
  • 4. Men and women of reproductive potential not agreeing to use an acceptable method of birth control during treatment and for six months after completion of treatment.
  • 5. Patients with other severe medical problems and with an expected short survival for non-lymphoma reasons.
  • 6. Known HIV positivity.
  • 7. Present or previous cancer except basal cell carcinoma and cervical carcinoma in situ.
  • 8. Uncontrolled infectious disease.
  • 9. Psychiatric or mental disorder which make the patient unable to give an informed consent
  • and/or adhere to the protocol.

研究者

发起方
ordic Lymphoma Group

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