Phase III Intergroup Prospectively Randomized Trial of Perioperative 5-FU After Curative Resection, Followed by 5-FU/Leucovorin for Patients With Colon Cancer
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 发起方
- 入组人数
- 859
- 试验地点
- 1
- 主要终点
- 5-year Overall Survival Rate in Patients With Dukes' B3/C Disease
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 if surgery is more effective with or without chemotherapy for colon cancer.
PURPOSE: Randomized phase III trial to evaluate whether perioperative 5-Fluorouracil (5-FU) chemotherapy after curative resection could improve overall survival and disease-free survival in patients with Duke's B3 or C colon cancer.
详细描述
OBJECTIVES:
I. To determine if adjuvant therapy with one week of continuous 5-FU given within 24 hours of a curative colon resection followed by 6 months of 5-FU/leucovorin is effective in prolonging the disease-free survival and increasing overall survival in patients with Dukes' B3 or C colon cancer, when compared to patients who are treated with 5-FU/leucovorin only.
II. 1. To determine if a week of perioperative continuous 5-FU affects disease-free survival and overall survival in patients with Dukes' B2 colon cancer.
OUTLINE: This is an open-label, randomized phase III study. Patients undergo curative colon resection via laparotomy. Patients are randomized to 1 of 2 arms in a 1:1 ratio.
Arm I (Perioperative 5-FU): Within 24 hours of the colon resection, patients receive perioperative 5-fluorouracil (5-FU) intravenously (IV) over 24 hours for 7 days.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Adenocarcinoma of the colon documented by colonoscopy or barium enema
- •Tumor either considered resectable or totally resected within 24 hours prior to study
- •Randomization within 2 weeks prior to surgery or within 24 hours after surgery required
- •Patients randomized after surgery must meet the following criteria:
- •Complete resection performed with no evidence of residual disease or distant metastases
- •Distal margin of tumor above the peritoneal reflection in area of rectum
- •No free perforation Intestinal obstruction allowed
- •Preliminary or complementary colostomy allowed
- •Concurrent registration for E3293 strongly recommended
- •Age 18 and over
- •Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- •Adequate organ function based on the following tests within 2 weeks prior to randomization
- •White Blood Cell (WBC) at least 3,000/mm^3
- •Platelet count at least 100,000/mm^3
- •Bilirubin no greater than 2.0 mg/dL
- •Creatinine no greater than 2.0 mg/dL
- •No second malignancy within 5 years except: superficial non-melanomatous skin cancer and carcinoma in situ of the cervix
- •Fertile patients must use adequate contraception
排除标准
- •Dual primary tumors
- •Prior nonmalignant systemic disease that would preclude use of chemotherapy
- •Pregnant or nursing
- •Prior fluorouracil
- •Other prior or concurrent chemotherapy for this malignancy
- •Prior or concurrent radiotherapy for this malignancy
- •Eligibility Criteria for Re-registration for Patients Randomized Pre-operatively:
- •Must have pathologic classification of Dukes' B2, B3, or C disease by the contributing institution.
- •Must be re-registered < 35 days after surgery.
- •ECOG performance status of 0-
- •Complete resection must have been performed with no evidence of residual disease or distant metastasis.
- •Distal margin of the tumor must not extend below the peritoneal reflection in the area of the rectum.
- •Single primary colon carcinoma without free perforation demonstrated. Patients with intestinal obstruction are eligible. Preliminary or complementary colostomy dose not preclude entry of a patient.
- •Have WBC > 3000/mm^3, platelets > 100,000/mm^3, adequate renal (serum creatinine <= 2.0mg/dL) and hepatic function (bilirubin <= 2.0mg/dL), within one week prior to beginning adjuvant chemotherapy (For Dukes' B3 and C patients only).
- •Eligibility Criteria for Re-registration for Patients Randomized Post-operatively:
- •Must have pathologic classification of Dukes' B2, B3, or C disease by the contributing institution.
- •Patient must be re-registered < 35 days after surgery.
- •ECOG performance status of 0-
- •Started perioperative 5-FU, if assigned, within 24 hours of surgery.
- •Have WBC > 3000/mm^3, platelets > 100,000/mm^3, adequate renal (serum creatinine <= 2.0mg/dL) and hepatic function (bilirubin < =2.0mg/dL), within one week prior to beginning adjuvant chemotherapy (For Dukes' B3 and C patients only).
研究组 & 干预措施
Perioperative 5-FU
Within 24 hours of the colon resection, patients receive perioperative fluorouracil intravenously (IV) over 24 hours for 7 days.
After surgery (beginning 21-35 days post-surgery), 5-FU was given at a dose of 425 mg/m^2 IV push on days 1-5, and leucovorin calcium was given at a dose of 20mg/m^2 IV push on days 1-5
干预措施: fluorouracil (Drug)
Perioperative 5-FU
Within 24 hours of the colon resection, patients receive perioperative fluorouracil intravenously (IV) over 24 hours for 7 days.
After surgery (beginning 21-35 days post-surgery), 5-FU was given at a dose of 425 mg/m^2 IV push on days 1-5, and leucovorin calcium was given at a dose of 20mg/m^2 IV push on days 1-5
干预措施: leucovorin calcium (Drug)
No perioperative 5-FU
Patients receive no perioperative fluorouracil.
After surgery (beginning 21-35 days post-surgery), 5-FU was given at a dose of 425 mg/m^2 IV push on days 1-5, and leucovorin calcium was given at a dose of 20mg/m^2 IV push on days 1-5
干预措施: fluorouracil (Drug)
No perioperative 5-FU
Patients receive no perioperative fluorouracil.
After surgery (beginning 21-35 days post-surgery), 5-FU was given at a dose of 425 mg/m^2 IV push on days 1-5, and leucovorin calcium was given at a dose of 20mg/m^2 IV push on days 1-5
干预措施: leucovorin calcium (Drug)
结局指标
主要结局
5-year Overall Survival Rate in Patients With Dukes' B3/C Disease
时间窗: every 3 months for 2 years, then every 6 months for 2 years, and then annually until year 15 after randomization
Overall survival (OS) is defined as time from randomization to death from any cause or last date known alive. Kaplan-Meier method was used to estimate 5-year OS rate
次要结局
- 5-year Disease-free Survival Rate in Patients With Dukes' B3/C Disease(every 3 months for 2 years, then every 6 months for 2 years, and then annually until year 15 after randomization)
- 5-year Overall Survival Rate in Patients With Dukes' B2 Disease(every 3 months for 2 years, then every 6 months for 2 years, and then annually until year 15 after randomization)
- 5-year Disease-free Survival Rate in Patients With Dukes' B2 Disease(every 3 months for 2 years, then every 6 months for 2 years, and then annually until year 15 after randomization)