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临床试验/NCT00392314
NCT00392314已完成2 期

Phase 2 Study.Tailored Therapy for Hodgkin Lymphoma Based on Predefined Risk Factors and Early Interim PET/CT for Response Assessment and Further Therapy Decisions.

Rambam Health Care Campus2 个研究点 分布在 1 个国家目标入组 365 人开始时间: 2006年10月最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
365
试验地点
2
主要终点
Event Free Survival

研究概览

简要总结

Recently published studies demonstrated very high event free survival for patients with a normal interim PET/CT and a high hazard ratio for progression of an interim positive (pathological)study. These findings strongly support the integration of interim PET as a decision point for adjustment of chemotherapy.This study use the minimal therapy considered safe according to the predefined risk factors for patients with interim negative PET. Those with pathologic interim study considered as higher risk patients will have dose escalation of therapy.remission rate ,event free survival and overall survival will be evaluated.

详细描述

study aim is to tailor the therapy in order to administer the lowest cumulative dose of therapy yet considered safe in order to reduce both early and late therapy related complications.

patients will be divided according to risk factors to sub groups of early favorable, early unfavorable, advanced disease with score less then 3 points or higher then 3 points.

Early Interim PET will be carried out Further therapy will be based on the study results.

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 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Hodgkin lymphoma patients
  • age 18-60 for those with early disease and advanced disease with score less then 3
  • age 18-60 years for patients with advanced disease score 3 or higher classical Hodgkin lymphoma
  • WBC more then 3500
  • platelets more then 100000
  • creatinin less then 2.0 mg
  • bilirubin less then 2.0 mg
  • absolute neutrophil count more then 1000 unless bone marrow involvement If marrow involve, patient with lower count but ANC of 1000 may be included.

排除标准

  • Positive serology for HIV
  • bilirubin more then 2 mg/dl
  • creatinin more then 2 mg/dl
  • lactating woman or pregnant
  • patient older then 60 years with high risk disease of score 3 or more

结局指标

主要结局

Event Free Survival

时间窗: 5 years

Event Free survival in various risk groups of patients

时间窗: five years

次要结局

  • overall survival5 years(5 years)
  • event free survival 5 years(five years)
  • Disease free survival 5 years(five years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

e_dann

Eldad J Dann assoc Prof of Hematology (Clinical), director of blood bank and aphaeresis unit RAMBAM health care campus Haifa Israel

Rambam Health Care Campus

研究点 (2)

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