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临床试验/NCT00003029
NCT00003029已完成3 期

Infusional 5-Fluorouracil With or Without Cisplatin and With or Without Chronomodulation Against Locally-Advanced or Metastatic Pancreatic Cancer. A Multicenter Randomized Phase III Trial.

European Organisation for Research and Treatment of Cancer - EORTC19 个研究点 分布在 5 个国家目标入组 200 人开始时间: 1997年5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
200
试验地点
19

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 and giving drugs in different ways may kill more tumor cells. It is not yet known whether fluorouracil plus cisplatin are more effective than fluorouracil alone in treating patients with metastatic cancer of the pancreas.

PURPOSE: Randomized phase III trial to compare the effectiveness of fluorouracil with or without cisplatin in treating patients who have advanced or metastatic cancer of the pancreas.

详细描述

OBJECTIVES:

  • Confirm the value of chronomodulated infusion with respect to survival in patients with locally advanced or metastatic pancreatic cancer.
  • Test the value of adding cisplatin to fluorouracil in extending survival in these patients.

OUTLINE: This is a multicenter, randomized study.

The study design is a 2 X 2 factorial such that patients are allocated to one of 4 treatment groups involving the use or absence of chronomodulation and cisplatin (CDDP). Treatment in each of the 4 groups is repeated for 3 courses where each course is a 5-day course of treatment.

Patients in the first group receive a chronomodulated schedule based on delivery of fluorouracil (FU). Patients in the second group receive a chronomodulated schedule of FU and CDDP. Patients in the third and fourth experimental groups receive flat schedules of FU alone or FU and CDDP, respectively. Dosages of FU are increased across the three courses whereas dosages of CDDP remain constant.

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:
  • •Histologic or cytologic proof of adenocarcinoma of the exocrine pancreas or of a metastasis associated with a radiologically identified pancreatic tumor
  • •Locally advanced and/or metastatic pancreatic cancer
  • •No measurable or evaluable target lesion is required
  • •No brain metastasis
  • •PATIENT CHARACTERISTICS:
  • •18 and over
  • •Performance status:
  • •Karnofsky 40%-100%
  • •Hematopoietic:
  • •WBC at least 3,000/mm^3
  • •Neutrophil count at least 1,500/mm^3
  • •Platelet count at least 100,000/mm^3
  • •Bilirubin no greater than 3 times normal
  • •Creatinine no greater than 1.24 mg/dL OR
  • •Creatinine clearance at least 80 mL/min
  • •Cardiovascular:
  • •No overt cardiac disease
  • •No peripheral neuropathy
  • •No uncontrolled infectious or chronic disease
  • •No second primary except in situ carcinoma of the cervix, or basal or squamous cell carcinoma of the skin
  • •PRIOR CONCURRENT THERAPY:
  • •Biologic therapy:
  • •No concurrent immunologic therapy
  • •Chemotherapy:
  • •No prior chemotherapy allowed
  • •Endocrine therapy:
  • •No concurrent hormonal therapy
  • •At least 2 weeks since corticoid treatment
  • •Radiotherapy:
  • •No prior radiotherapy allowed except as an analgesic treatment on metastasis
  • •Not specified

排除标准

  • 未提供

研究者

申办方类型
Network
责任方
Sponsor

研究点 (19)

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