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临床试验/NCT00227695
NCT00227695已完成3 期

Comparing Two Schedules of Rituximab Maintenance in Rituximab-Responding Patients With Untreated, Chemotherapy Resistant or Relapsed Follicular Lymphoma: A Randomized Phase III Trial

Swiss Group for Clinical Cancer Research51 个研究点 分布在 7 个国家目标入组 270 人开始时间: 2004年6月8日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
270
试验地点
51
主要终点
Event-free survival

研究概览

简要总结

RATIONALE: Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. It is not yet known whether giving rituximab over a short period of time is more effective than giving it over a long period of time in treating follicular non-Hodgkin's lymphoma.

PURPOSE: This randomized phase III trial is studying rituximab to see how well it works when given over a short period of time compared to when given over a long period of time in treating patients with follicular non-Hodgkin's lymphoma.

详细描述

OBJECTIVES:

Primary

  • Compare the efficacy of induction therapy with rituximab followed by short- vs long-term maintenance therapy with rituximab, in terms of event-free survival, in patients with follicular non-Hodgkin's lymphoma.

Secondary

  • Compare the safety of these regimens in these patients.
  • Compare the pharmaeconomical aspects of these regimens in these patients.
  • Compare the evolution of immunologic competence in patients treated with these regimens.

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
18 Years 至 —(Adult, Older 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

Arm A: Rituximab every 2 months x4

Active Comparator

Rituximab 375 mg/m2 every 2 months x4

干预措施: rituximab (Biological)

Arm B: Rituximab (5 years)

Active Comparator

Rituximab 375 mg/m2 every 2 months for 5 years or until PD, relapse or unacceptable toxicity

干预措施: rituximab (Biological)

结局指标

主要结局

Event-free survival

时间窗: at 10 years

次要结局

  • Overall survival(at 10 years)
  • Progression-free survival(at 10 years)
  • Adverse reactions during and after maintenance treatment(10 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (51)

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