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临床试验/NCT00006455
NCT00006455已完成3 期

International Protocol for the Treatment of Childhood Anaplastic Large Cell Lymphoma

Gustave Roussy, Cancer Campus, Grand Paris20 个研究点 分布在 10 个国家目标入组 885 人开始时间: 1999年11月26日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
885
试验地点
20
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 tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. It is not yet known which combination chemotherapy regimen is more effective for treating anaplastic large cell lymphoma.

PURPOSE: This randomized phase III trial is studying several different regimens of combination chemotherapy to compare how well they work in treating children with anaplastic large cell lymphoma.

详细描述

OBJECTIVES:

  • Compare the event-free survival in children with anaplastic large cell lymphoma treated with various induction and maintenance chemotherapy regimens with or without vinblastine.
  • Compare the impact of different doses and schedules of methotrexate from the Berlin-Frankfurt-Munster-K2 Protocol in terms of overall survival, complete remission rate, CNS relapse rate, and nonlymphoma-related death and early death rates in these patients.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to country, vinblastine (VBL) (yes vs no), and prognostic factors (standard-risk (SR) vs high-risk (HR) disease).

Beginning immediately after confirmation of diagnosis, patients receive prephase therapy comprising dexamethasone (DM) IV or orally daily on days 1 and 2 and every 12 hours on days 3-5; cyclophosphamide (CTX) IV over 1 hour on days 1 and 2; and methotrexate (MTX) intrathecally (IT), doxorubicin (DOX) IV, and hydrocortisone (HC) IT on day 1.

Patients are then assigned to one of two treatment groups based on prognosis:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment

入排标准

年龄范围
0 Years 至 21 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

结局指标

主要结局

Event-free survival

次要结局

  • Nonlymphoma related death and early deaths (excluding deaths occurring after second-line treatment for failure or relapse)
  • Overall survival
  • CNS relapses
  • Complete remission achieved after treatment course B3 and lasting ≥ 4 weeks
  • Short- and long-term toxicity

研究者

申办方类型
Other
责任方
Sponsor

研究点 (20)

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