A Randomised Study Comparing CIDEX (CCNU, Oral Idarubicin and Dexamethasone) With Melphalan and Prednisolone in Relapsed Multiple Myeloma
试验速览
- 阶段
- 3 期
- 发起方
- 入组人数
- 660
- 试验地点
- 2
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. Steroids, such as dexamethasone or prednisolone, may help relieve some of the side effects of chemotherapy. It is not yet known which regimen of chemotherapy plus steroid therapy is more effective in treating patients with multiple myeloma.
PURPOSE: Randomized phase III trial to compare the effectiveness of two different regimens of chemotherapy plus steroid therapy in treating patients with multiple myeloma that has recurred for the first time.
详细描述
OBJECTIVES:
- Compare the response rate, response duration, and survival of patients with relapsed multiple myeloma after treatment with lomustine, idarubicin, and dexamethasone vs melphalan and prednisolone.
OUTLINE: This is a randomized study. Patients are stratified according to prior autologous transplant (yes vs no). Patients are randomized to one of two treatment arms.
- Arm I: Patients receive oral lomustine on day 1, oral idarubicin once daily on days 1-3, and oral dexamethasone twice a day on days 1-4. Treatment is repeated every 28 days for 6-9 courses in the absence of unacceptable toxicity or disease progression.
- Arm II: Patients receive oral melphalan once daily on days 1-4 and oral prednisolone twice a day on days 1-4. Treatment is repeated every 28 days for 6-9 courses in the absence of unacceptable toxicity or disease progression.
Some patients may receive oral cyclophosphamide every 7 days and oral prednisolone on alternate days for 6 weeks concurrently with chemotherapy in either treatment arm.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 主要目的
- Treatment
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •DISEASE CHARACTERISTICS:
- •Diagnosis of multiple myeloma based on at least two of the following:
- •Paraprotein in serum and/or urine
- •Greater than 10% plasma cells in bone marrow
- •Lytic bone lesions
- •Measurable serum and/or urine paraprotein
- •Progression from first or second stable plateau phase
- •No non-secretory myeloma or plasma cell leukemia (greater than 2,000/mm^3 circulating plasma cells)
- •No primary refractory disease or second or later relapse
- •PATIENT CHARACTERISTICS:
- •18 and over
- •Performance status:
- •Life expectancy:
- •Not specified
- •Hematopoietic:
- •Neutrophil count at least 1,000/mm^3
- •Platelet count at least 75,000/mm^3
- •Bilirubin no greater than 1.5 times upper limit of normal (ULN)
- •ALT/AST no greater than 2.5 times ULN
- •Creatinine less than 3.4 mg/dL
- •Cardiovascular:
- •No clinically significant cardiac insufficiency
- •No uncontrolled hypertension
- •No uncontrolled diabetes mellitus
- •No recent history of peptic ulceration
- •HIV-1 and HIV-2 negative
- •Fertile patients must use effective contraception during and for 6 months after study participation
- •PRIOR CONCURRENT THERAPY:
- •Biologic therapy:
- •No prior allogeneic peripheral blood stem cell or bone marrow transplantation
- •No planned future autologous transplantation unless sufficient stored stem cells available
- •Prior interferon allowed if administered as maintenance of stable plateau phase
- •No concurrent epoetin alfa
- •Chemotherapy:
- •At least 3 months since prior chemotherapy
- •Endocrine therapy:
- •Not specified
- •Radiotherapy:
- •Concurrent radiotherapy for pain or to treat localized tumors allowed
- •Not specified
- •No prior participation in any clinical trial with an unlicensed product
排除标准
- 未提供