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Spots Global Cancer Trial Database for Neoadjuvant Radiation Therapy and Capecitabine in Treating Patients With Stage III or Stage IV Colorectal Adenocarcinoma

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Trial Identification

Brief Title: Neoadjuvant Radiation Therapy and Capecitabine in Treating Patients With Stage III or Stage IV Colorectal Adenocarcinoma

Official Title: Phase II Study Of Radiotherapy And Capecitabine As Pre-Operative Treatment In Patients With Colorectal Cancer

Study ID: NCT00075556

Study Description

Brief Summary: RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs used in chemotherapy, such as capecitabine, use different ways to stop tumor cells from dividing so they stop growing or die. Combining radiation therapy with chemotherapy before surgery may shrink the tumor so that it can be removed. PURPOSE: This phase II trial is studying how well neoadjuvant radiation therapy and capecitabine work in treating patients who are undergoing surgery for stage III or stage IV colorectal adenocarcinoma.

Detailed Description: OBJECTIVES: Primary * Determine the objective tumor response rate in patients with stage III or IV colorectal adenocarcinoma treated with neoadjuvant radiotherapy and capecitabine. Secondary * Determine the tolerance profile of this regimen in these patients. * Determine the rate of preservation of functional integrity of the anal sphincter in patients treated with this regimen. * Compare the conversion rate from the effects of mutilating surgery vs surgery with sphincter preservation in patients treated with this regimen. OUTLINE: This is a multicenter study. Patients receive oral capecitabine twice daily and undergo concurrent radiotherapy 5 days a week on weeks 1-5. Patients undergo surgery on week 6. Patients are followed every 4 months for 2 years and then every 6 months for 3 years. PROJECTED ACCRUAL: A total of 48 patients will be accrued for this study within 10 months.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Centre Regional Francois Baclesse, Caen, , France

Hopital Drevon, Dijon, , France

Hopital Saint - Louis, La Rochelle, , France

Centre Jean Bernard, Le Mans, , France

Clinique Saint Jean, Lyon, , France

Hopital Notre-Dame de Bon Secours, Metz, , France

Intercommunal Hospital, Montfermeil, , France

Centre Hospitalier de Mulhouse, Mulhouse, , France

Hopital Saint-Louis, Paris, , France

Hopital Tenon, Paris, , France

C.H. Senlis, Senlis, , France

Centre Medico-Chirurgical Foch, Suresnes, , France

Contact Details

Name: Olivier Dupuis, MD

Affiliation: Centre Jean Bernard

Role:

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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