Randomised Trial Of Single Agent Doxorubicin Versus Doxorubicin Plus Ifosfamide In The First Line Treatment Of Advanced Or Metastatic Soft Tissue Sarcoma
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 455
- 试验地点
- 41
- 主要终点
- Overall survival
研究概览
简要总结
RATIONALE: Drugs used in chemotherapy such as doxorubicin and ifosfamide use different ways to stop tumor cells from dividing so they stop growing or die. Colony-stimulating factors, such as pegfilgrastim, cause the body to make blood cells. It is not yet known whether doxorubicin alone is more effective with or without ifosfamide and pegfilgrastim in treating soft tissue sarcoma.
PURPOSE: This randomized phase III trial is studying giving doxorubicin alone to see how well it works compared to giving doxorubicin together with ifosfamide and pegfilgrastim in treating patients with locally advanced or metastatic soft tissue sarcoma.
详细描述
OBJECTIVES:
- Compare the progression-free and overall survival of patients with locally advanced or metastatic soft tissue sarcoma treated with doxorubicin with vs without ifosfamide and pegfilgrastim as first-line therapy.
- Compare the response in patients treated with these regimens.
- Compare the treatment-related mortality of patients treated with these regimens.
- Compare the toxicity of these regimens in these patients.
OUTLINE: This is a randomized, open-label, multicenter study. Patients are stratified according to WHO performance status (0 vs 1), age group (less than 50 years of age vs 50 years of age and over), presence of liver metastases (yes vs no), histological grade (2 vs 3), and participating center. Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive doxorubicin IV on day 1 (or IV continuously on days 1-3).
- Arm II: Patients receive doxorubicin IV on days 1-3 and ifosfamide IV over 4 hours on days 1-4. Patients also receive pegfilgrastim subcutaneously on day 5.
In both arms, treatment repeats every 3 weeks for up to 6 courses in the absence of disease progression or unacceptable toxicity.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •DISEASE CHARACTERISTICS:
- •Histologically confirmed soft tissue sarcoma
- •Locally advanced unresectable* OR metastatic disease
- •High-grade (grade 2-3) disease according to the FNLCC grading system NOTE: *Disease that could prove resectable (including pulmonary metastasectomy) after a response to chemotherapy is allowed
- •The following tumor types are eligible:
- •Malignant fibrous histiocytoma
- •Myxoid and round cell liposarcoma, pleomorphic liposarcoma, or dedifferentiated liposarcoma
- •Pleomorphic rhabdomyosarcoma
- •Synovial sarcoma
- •Myxofibrosarcoma, intermediate and high-grade
- •Fibrosarcoma
- •Leiomyosarcoma
- •Angiosarcoma
- •Malignant peripheral nerve sheath tumor
- •Epithelioid sarcoma
- •Alveolar rhabdomyosarcoma
- •Unclassifiable sarcoma, not otherwise specified
- •The following tumor types are not eligible:
- •Gastrointestinal stromal tumor
- •Mixed mesodermal tumor
- •Chondrosarcoma
- •Malignant mesothelioma
- •Neuroblastoma
- •Osteosarcoma
- •Ewing's sarcoma/primitive neuroectodermal tumor
- •Desmoplastic small round cell tumor
- •Embryonal rhabdomyosarcoma
- •Alveolar soft part sarcoma
- •Must have a measurable lesion with clinical evidence of progression within the past 6 weeks
- •Osseous lesions and pleural effusions are not considered measurable
- •No known or symptomatic CNS metastases
- •PATIENT CHARACTERISTICS:
- •Performance status
- •Life expectancy
- •Not specified
- •Hematopoietic
- •Absolute neutrophil count at least 2,000/mm^3
- •Platelet count at least 100,000/mm^3
- •Bilirubin no greater than 1.8 mg/dL
- •Albumin at least 2.5 g/dL
- •Creatinine no greater than 1.4 mg/dL OR
- •Creatinine clearance greater than 65 mL/min
- •Cardiovascular
- •No history of cardiovascular disease
- •Not pregnant
- •Negative pregnancy test
- •Fertile patients must use effective contraception
- •No other severe medical illness
- •No psychosis
- •No other prior or concurrent malignancy except adequately treated carcinoma in situ of the cervix or basal cell skin cancer
- 另有 12 项未显示
排除标准
- 未提供
结局指标
主要结局
Overall survival
次要结局
- Response as assessed by RECIST criteria
- Toxicity as assessed by CTC 2.0
- Treatment-related mortality