Radiation Therapy and Capecitabine With or Without Oxaliplatin in Treating Patients Who Are Undergoing Surgery for Stage II or Stage III Rectal Cancer
- Conditions
- Colorectal Cancer
- Interventions
- Procedure: conventional surgeryProcedure: neoadjuvant therapyRadiation: radiation therapy
- Registration Number
- NCT00227747
- Lead Sponsor
- UNICANCER
- Brief Summary
RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs used in chemotherapy, such as capecitabine and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells. Giving radiation therapy together with combination chemotherapy before surgery may shrink the tumor so it can be removed. It is not yet known whether giving radiation therapy together with capecitabine is more effective with or without oxaliplatin before surgery in treating rectal cancer.
PURPOSE: This randomized phase III trial is studying radiation therapy, capecitabine, and oxaliplatin to see how well they work compared to radiation therapy and capecitabine in treating patients who are undergoing surgery for stage II or stage III rectal cancer.
- Detailed Description
OBJECTIVES:
Primary
* Compare the efficacy of neoadjuvant chemoradiotherapy comprising radiotherapy and capecitabine with vs without oxaliplatin followed by total mesorectal excision, in terms of the rate of complete surgical resection, in patients with resectable stage II or III rectal cancer.
Secondary
* Compare overall and disease-free survival of patients treated with these regimens.
* Compare clinical tumor response in patients treated with these regimens.
* Compare acute and late toxicity of these regimens in these patients.
* Determine biological parameters that predict tumor response and treatment-related toxicity in patients treated with these regimens.
* Compare sphincter preservation and function in patients treated with these regimens.
OUTLINE: This is a randomized, controlled, multicenter study. Patients are randomized to 1 of 2 treatment arms.
* Arm I: Patients undergo radiotherapy once daily 5 days a week and receive capecitabine once daily 5 days a week in weeks 1-5.
* Arm II: Patient undergo radiotherapy and receive capecitabine as in arm I. Patients also receive oxaliplatin once weekly in weeks 1-5.
All patients undergo total mesorectal excision 6 weeks after completion of chemoradiotherapy.
PROJECTED ACCRUAL: A total of 590 patients will be accrued for this study.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 598
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Radiothérapie + Xelox capecitabine - Radiothérapie + Xelox oxaliplatin - Radiothérapie + Xelox conventional surgery - Radiothérapie + Xelox neoadjuvant therapy - Radiothérapie + Xelox radiation therapy - Radiothérapie + Capécitabine capecitabine - Radiothérapie + Capécitabine conventional surgery - Radiothérapie + Capécitabine neoadjuvant therapy - Radiothérapie + Capécitabine radiation therapy -
- Primary Outcome Measures
Name Time Method Rate of complete surgical resection
- Secondary Outcome Measures
Name Time Method Overall survival Disease-free survival Sphincter preservation Sphincter function Biological parameters that predict tumor response and treatment-related toxicity Acute and late toxicity
Trial Locations
- Locations (68)
Centre Hospitalier d'Abbeville
🇫🇷Abbeville, France
Centre Hospitalier
🇫🇷Altkirch, France
Institut Sainte Catherine
🇫🇷Avignon, France
Hopital Duffaut
🇫🇷Avignon, France
Hopital de Beziers
🇫🇷Beziers, France
Centre Hospitalier de Blois
🇫🇷Blois, France
Hopital Saint Andre
🇫🇷Bordeaux, France
Institut Bergonie
🇫🇷Bordeaux, France
Polyclinique Bordeaux Nord Aquitaine
🇫🇷Bordeaux, France
Clinique Tivoli
🇫🇷Bordeaux, France
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