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临床试验/NCT00049595
NCT00049595已完成3 期

BEACOPP (4 Cycles Escalated + 4 Cycles Baseline) Versus ABVD (8 Cycles) In Stage III & IV Hodgkin's Lymphoma

European Organisation for Research and Treatment of Cancer - EORTC140 个研究点 分布在 6 个国家目标入组 552 人开始时间: 2002年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
552
试验地点
140
主要终点
Event-free survival

研究概览

简要总结

RATIONALE: Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Combining more than one drug may kill more cancer cells. It is not yet known which combination chemotherapy regimen is more effective in treating stage III or stage IV Hodgkin's lymphoma.

PURPOSE: Randomized phase III trial to compare the effectiveness of two combination chemotherapy regimens in treating patients who have stage III or stage IV Hodgkin's lymphoma.

详细描述

OBJECTIVES:

  • Compare event-free survival of patients with stage III or IV Hodgkin's lymphoma treated with bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone vs doxorubicin, bleomycin, vinblastine, and dacarbazine.
  • Compare complete response, disease-free survival, and overall survival of patients treated with these regimens.
  • Compare quality of life of patients treated with these regimens.
  • Compare occurrence of second malignancies in patients treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to International Prognostic Score (3 vs 4 or more) and participating center. Patients are randomized to 1 of 2 treatment arms.

  • Arm I (BEACOPP): Patients receive doxorubicin IV over 5 minutes and cyclophosphamide IV on day 1; etoposide IV over 30 minutes on days 1-3; oral procarbazine on days 1-7; oral prednisone on days 1-14; and vincristine IV and bleomycin IV or intramuscularly (IM) on day 8. Patients may receive dexamethasone in place of prednisone. Patients also receive filgrastim (G-CSF) subcutaneously (SC) beginning on day 9 and continuing until blood counts recover or pegfilgrastim SC on day 9 only. Treatment repeats every 22 days for 8 courses (4 courses escalated dose followed by 4 courses baseline dose) in the absence of disease progression or unacceptable toxicity.
  • Arm II (ABVD): Patients receive doxorubicin IV over 5 minutes, bleomycin IV or IM, vinblastine IV, and dacarbazine IV over 5-10 minutes on days 1 and 15. Treatment repeats every 28 days for 8 courses in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline, at the end of therapy, and then annually for 10 years.

研究设计

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

入排标准

年龄范围
16 Years 至 60 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: filgrastim (Biological)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: bleomycin sulfate (Biological)

ABVD

Active Comparator

8 cycles of ABVD

干预措施: bleomycin sulfate (Biological)

ABVD

Active Comparator

8 cycles of ABVD

干预措施: ABVD regimen (Drug)

ABVD

Active Comparator

8 cycles of ABVD

干预措施: dacarbazine (Drug)

ABVD

Active Comparator

8 cycles of ABVD

干预措施: doxorubicin hydrochloride (Drug)

ABVD

Active Comparator

8 cycles of ABVD

干预措施: vinblastine sulfate (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: pegfilgrastim (Biological)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: BEACOPP regimen (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: cyclophosphamide (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: doxorubicin hydrochloride (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: etoposide (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: prednisone (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: procarbazine hydrochloride (Drug)

BEACOPP

Experimental

4 cycles of BEACOPP Escalated + 4 cycles of BEACOPP Baseline

干预措施: vincristine sulfate (Drug)

结局指标

主要结局

Event-free survival

时间窗: from randomization to early discontinuation of protocol treatment, no CR/CRu after 8 cycles, relapse, progression or death

次要结局

  • Complete response as assessed by Cheson criteria adapted to Hodgkin's lymphoma(from randomization till end of treatment)
  • Disease-free survival in patients with complete response(from the day of first documentation of CR to the day of relapse)
  • Overall survival(from the date of randomization to the date of death)
  • Quality of life as assessed by European Organization for Research of the Treatment of Cancer (EORTC) Quality of Life Questionnaire (QoLQ) C30 version 3.0(from one week prior to randomization till 10 years after end of treatment or death)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (140)

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