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临床试验/NCT00647049
NCT00647049Unknown2 期

Freiburg ZNS-NHL Study: Therapy for Patients With Primary Non-Hodgkin Lymphoma of the CNS - Sequential High Dosage Chemotherapy With Autologous Peripheral Blood Stem Cell Plantation

University Hospital Freiburg1 个研究点 分布在 1 个国家目标入组 78 人开始时间: 2007年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
78
试验地点
1
主要终点
Complete response rate

研究概览

简要总结

The purpose of this study is to determine whether combined chemotherapy [rituximab plus high dosage methotrexate (max. 2 cycles) followed by arabinoside/thiotepa (max. 2 cycles) followed by high dosage carmustin/thiotepa] followed by peripheral blood stem cell transplantation is effective in the treatment of cerebral Non Hodgkin lymphoma [PCNSL].

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • group A: first diagnosis of PCNSL, histologically confirmed
  • group B: relapse or progression of PCNSL after MTX containing chemotherapy
  • age 18 - 65 years
  • not legally incompetent, physically or mentally incapable of giving consent
  • written signed and dated informed consent of the legal representative and - if possible - of the patient

排除标准

  • manifestations of further lymphoma outside the CNS
  • sero-positive for HIV
  • severe pulmonary, cardiac, hepatic, renal impairment
  • neutrophil count < 2.000/µl, platelet count < 100.000/µl
  • pulmonary disease with IVC < 55%, DLCO < 40%
  • cardiac ejection fraction < 50%, uncontrolled malign arrhythmia
  • creatinine > 1,5 mg% or creatinine-clearance < 50ml/min
  • bilirubin > 2mg/dl
  • ascites or pleural effusion (> 500ml)
  • pregnancy o r lactation
  • women with childbearing potential without sufficient contraception
  • participation in another clinical trial within the last 30 days prior to the begin or parallel to this study
  • known or current drug or alcohol abuse
  • known hypersensitivity against methotrexate, cytarabine, thiotepa, BCNU rituximab, leukovorin, dexamethasone, neupogen and neulasta.

研究组 & 干预措施

A

Experimental

first diagnosis of PCNSL: combined chemotherapy with methotrexate

干预措施: methotrexate (Drug)

A

Experimental

first diagnosis of PCNSL: combined chemotherapy with methotrexate

干预措施: Rituximab (Drug)

A

Experimental

first diagnosis of PCNSL: combined chemotherapy with methotrexate

干预措施: Cytarabine (Drug)

A

Experimental

first diagnosis of PCNSL: combined chemotherapy with methotrexate

干预措施: Thiotepa (Drug)

A

Experimental

first diagnosis of PCNSL: combined chemotherapy with methotrexate

干预措施: Carmustin (Drug)

B

Experimental

Patients with relapse or progressive disease of PCNSL after methotrexate containing chemotherapy

干预措施: Rituximab (Drug)

B

Experimental

Patients with relapse or progressive disease of PCNSL after methotrexate containing chemotherapy

干预措施: Cytarabine (Drug)

B

Experimental

Patients with relapse or progressive disease of PCNSL after methotrexate containing chemotherapy

干预措施: Thiotepa (Drug)

B

Experimental

Patients with relapse or progressive disease of PCNSL after methotrexate containing chemotherapy

干预措施: Carmustin (Drug)

结局指标

主要结局

Complete response rate

时间窗: 30 days after blood stem cell transplantation

次要结局

  • Duration of response(within 5 years)
  • Overall survival time(within 5 years)
  • Neuropsychological state according to Mini-Mental State(within 5 years)
  • Neuropsychological assessment (digit span, Hopkins verbal Learning Test-Revised, Trials 1-3, Brief Test of Attention, Trial Making Test, Grooved Pegboard, 6. HVLT-R , EORTC L C30 , EORTC BN20)(within 5 years)
  • (Serious) adverse events ([S]AEs)(within 30 days after treatment)

研究者

发起方
University Hospital Freiburg
申办方类型
Other

研究点 (1)

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