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临床试验/NCT00002539
NCT00002539已完成3 期

A RANDOMISED TRIAL OF CHEMOTHERAPY WITH OR WITHOUT GRANULOCYTE COLONY-STIMULATING FACTOR IN OPERABLE OSTEOSARCOMA

European Organisation for Research and Treatment of Cancer - EORTC32 个研究点 分布在 8 个国家目标入组 214 人开始时间: 1993年8月1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
214
试验地点
32

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. Colony-stimulating factors such as G-CSF may increase the number of immune cells found in bone marrow or peripheral blood and may help a person's immune system recover from the side effects of chemotherapy. It is not yet known whether chemotherapy and surgery plus G-CSF is more effective than chemotherapy and surgery alone in treating patients with osteosarcoma.

PURPOSE: Randomized phase III trial to compare the effectiveness combination chemotherapy and surgery with or without G-CSF in treating patients who have newly diagnosed osteosarcoma.

详细描述

OBJECTIVES:

  • Determine the overall and disease-free survival of patients with newly diagnosed osteosarcoma of the extremity treated with conventional vs intensive cisplatin and doxorubicin with or without filgrastim (G-CSF) before and after definitive surgery.
  • Compare the toxicity of these regimens in these patients.
  • Compare the response in patients treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive conventional doxorubicin (DOX) IV over 4 hours on days 1-3 and cisplatin (CDDP) IV continuously on day 1. Treatment continues every 3 weeks for 2 courses. At week 6, patients undergo amputation or local resection based on pretherapy imaging and response to chemotherapy. Beginning 2 weeks after surgery, patients receive 4 additional courses of conventional chemotherapy.
  • Arm II: Patients receive intensive DOX and CDDP as above on day 1 plus filgrastim (G-CSF) subcutaneously on days 4-13. Treatment continues every 2 weeks for 3 courses. At week 6, patients undergo definitive surgery as in arm I. Beginning 2 weeks after surgery, patients receive 3 additional courses of intensive DOX and CDDP with G-CSF.

Patients who experience disease progression during preoperative chemotherapy undergo surgery earlier than scheduled and complete all scheduled chemotherapy (6 courses) after surgery, at the discretion of the surgeon and oncologist. Within 4 weeks after limb-sparing procedure, patients with inadequate margins undergo amputation, followed 2 weeks later by chemotherapy.

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
— 至 40 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • DISEASE CHARACTERISTICS:
  • Histologically proven resectable osteosarcoma of the long bone of an extremity
  • No parosteal (juxtacortical), periosteal, Pagetoid, or post-irradiation sarcoma
  • No distant metastases
  • PATIENT CHARACTERISTICS:
  • 40 and under
  • Performance status:
  • Not specified
  • Life expectancy:
  • Not specified
  • Hematopoietic:
  • Neutrophil count at least 1,500/mm^3 OR
  • WBC at least 3,500/mm^3
  • Platelet count at least 100,000/mm^3
  • Bilirubin no greater than 1.2 mg/dL
  • Glomerular filtration rate at least 60 mL/min
  • Cardiovascular:
  • No history of cardiac dysfunction
  • No other prior or concurrent malignancy except basal cell skin cancer OR
  • Carcinoma in situ of the cervix
  • PRIOR CONCURRENT THERAPY:
  • Biologic therapy:
  • Not specified
  • Chemotherapy:
  • No other concurrent chemotherapy
  • Endocrine therapy:
  • Not specified
  • Radiotherapy:
  • See Disease Characteristics
  • See Disease Characteristics
  • No prior therapy

排除标准

  • 未提供

研究者

申办方类型
Network
责任方
Sponsor

研究点 (32)

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