NCT Number: NCT00002523
Radiation Therapy, Surgery, and Chemotherapy in Treating Patients With Rectal Cancer That Can Be Surgically Removed
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, giving the drugs in different ways, and combining radiation therapy and surgery with chemotherapy may kill more tumor cells.
PURPOSE: Randomized phase III trial to compare radiation therapy alone before surgery with radiation therapy plus fluorouracil and leucovorin before surgery, with and without fluorouracil and leucovorin after surgery in patients with rectal cancer that can be surgically removed.
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Notify MeKey information
Conditions
Age range
Up to 80 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Hopital Universitaire Erasme, Brussels, Belgium
About this study
OBJECTIVES:
- Compare the disease-free and overall survival in patients with resectable adenocarcinoma of the rectum treated with preoperative radiotherapy with or without preoperative fluorouracil (5-FU) combined with leucovorin calcium (CF) and/or postoperative 5-FU/CF.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to center, sex, tumor location (0-5 vs 6-10 vs 11-15 cm from anal margin), and stage (T3 vs T4). Patients are randomized to 1 of 4 treatment arms.
- Arm I: Patients undergo involved-field radiotherapy 5 days a week for 5 weeks followed 3-10 weeks later by abdominoperineal resection or anal-sparing resection according to local practice in the absence of disease progression or unacceptable toxicity.
- Arm II: Patients undergo radiotherapy as in arm I beginning on day 1 and leucovorin calcium (CF) IV followed by fluorouracil (5-FU) IV (1 hour before radiotherapy) on days 1-5 and 29-33, followed 3-10 weeks later by resection as in arm I in the absence of disease progression or unacceptable toxicity.
- Arm III: Patients undergo radiotherapy followed 3-10 weeks later by resection as in arm I. Within 3-10 weeks after resection, patients receive CF followed by 5-FU on days 1-5. Chemotherapy continues every 4 weeks for 4 courses in the absence of disease progression or unacceptable toxicity.
- Arm IV: Patients undergo preoperative radiotherapy with concurrent chemotherapy followed by resection as in arm II and postoperative chemotherapy as in arm III.
Patients are followed every 6 months.
PROJECTED ACCRUAL: A total of 992 patients will be accrued for this study within 4 years.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Histologically confirmed resectable adenocarcinoma of the rectum
- Any grade
- Tumor macroscopically within 15 cm of anal margin on rigid rectoscopy
- Tumor tethered or partially fixed on digital rectal exam and/or T3-4 on rectal ultrasound
- No acute or subacute bowel obstruction without colostomy diversion
- No chronic inflammatory disease of the ileum and/or colon
- No primary adenocarcinoma of the anal canal
- No distant metastasis
PATIENT CHARACTERISTICS:
Age:
- 80 and under
Performance status:
- WHO 0-1
Life expectancy:
- Not specified
Hematopoietic:
- Granulocyte count greater than 2,000/mm^3
- Platelet count greater than 130,000/mm^3
Hepatic:
- Not specified
Renal:
- Creatinine less than 1.36 mg/dL
Cardiovascular:
- No angina pectoris
Other:
- No other prior malignancy except basal cell skin cancer or carcinoma in situ of the uterine cervix
PRIOR CONCURRENT THERAPY:
Biologic therapy
- No prior biologic therapy for adenocarcinoma of the rectum
Chemotherapy
- No prior chemotherapy for adenocarcinoma of the rectum
Endocrine therapy
- No prior endocrine therapy for adenocarcinoma of the rectum
Radiotherapy
- No prior radiotherapy for adenocarcinoma of the rectum
Surgery
- No prior surgery for adenocarcinoma of the rectum
Treatment and study plan
leucovorin calcium
Drugconventional surgery
Procedureradiation therapy
RadiationSponsors and collaborators
Lead sponsor
European Organisation for Research and Treatment of Cancer - EORTC
Network
Registry information
Official study title
FOUR ARMS PHASE III CLINICAL TRIAL FOR T3-T4 RESECTABLE RECTAL CANCER COMPARING PRE-OPERATIVE PELVIC IRRADIATION TO PRE-OPERATIVE IRRADIATION COMBINED WITH FLUOROURACIL AND LEUCOVORIN WITH OR WITHOUT POST-OPERATIVE ADJUVANT CHEMOTHERAPY
Important dates
- Study start
- 1993
- Primary completion
- 2003
- Study completion
- 2016
- First posted
- Jan 27, 2003
- Registry last updated
- Sep 2, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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