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临床试验/NCT00002678
NCT00002678已完成3 期

Comparative Study of Dexamethasone vs Prednisone (Both in Combination With Melphalan) as Induction Therapy in Untreated Symptomatic Myeloma With an Additional Assessment of Dexamethasone vs no Additional Treatment as Maintenance Therapy in Non-Progressing Patients

NCIC Clinical Trials Group37 个研究点 分布在 2 个国家目标入组 595 人开始时间: 1995年6月2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
595
试验地点
37
主要终点
Overall 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 most effective in treating patients with multiple myeloma.

PURPOSE: Randomized phase III trial to compare the effectiveness of various combination chemotherapy regimens in treating patients with multiple myeloma.

详细描述

OBJECTIVES:

  • Compare the overall survival of patients with previously untreated stage I-III multiple myelome treated with melphalan combined with dexamethasone or prednisone as induction therapy.
  • Compare the overall survival of patients with stable or responding disease after induction treated with dexamethasone vs observation alone as maintenance therapy.
  • Compare the time to progression, response rate, and quality of life of patients treated with these regimens.
  • Compare the toxic effects of these regimens in these patients.

OUTLINE: This is a randomized, multicenter study. Patients are stratified by center, stage (I or II vs III), creatinine (less than 2.0 mg/dL vs 2.0 mg/dL or greater), and intention to use prophylactic bisphosphonate (yes vs no).

  • Induction: Patients are randomized to 1 of 4 treatment arms.

  • Arms I and II: Patients receive induction comprising oral prednisone followed by oral melphalan on days 1-4.

  • Arms III and IV: Patients receive induction comprising oral melphalan and oral dexamethasone (DM) on days 1-4 of all courses and DM on days 15-18 of courses 1-3.

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 120 Years(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

Melphan plus prednisone

Active Comparator

melphalan plus prednisone qd x 4 28 day cycles x 12 cycles; No treatment after stable response.

干预措施: melphalan (Drug)

Melphan plus prednisone

Active Comparator

melphalan plus prednisone qd x 4 28 day cycles x 12 cycles; No treatment after stable response.

干预措施: prednisone (Drug)

Melphan, prednisone pluse dexamethasone

Active Comparator

melphalan plus prednisone qd x 4 28 day cycles x 12 cycles; dexamethasone qd x 4 q 28 days after non-progression

干预措施: dexamethasone (Drug)

结局指标

主要结局

Overall survival

时间窗: 9 years

To compare overall survival between: i) patients receiving melphalan-prednisone and those receiving melphalan-dexamethasone as induction therapy ii) patients maintained by dexamethasone and those on no additional treatment in the subgroup whose disease has not progressed at the time of the 12th induction cycle

次要结局

  • Time to progression(9 years)
  • Response rates(9 years)
  • Toxicity(9 years)
  • Quality of Life(9 years)

研究者

申办方类型
Network
责任方
Sponsor

研究点 (37)

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