Study of Capecitabine and Oxaliplatin in Combination With Radiotherapy in Patients With Unresectable Gastro-Intestinal Cancer

Phase 1

Completed

• Conditions: Stomach Cancer; Gall Bladder Cancer; Bile Ductus Cancer; Pancreas Cancer; Colorectal Cancer
• Interventions: Other: oxaliplatin, capecitabine, radiotherapy

• Registration Number: NCT01016639
• Lead Sponsor: Lund University Hospital

Brief Summary

The purpose with this study is to evaluate treatment with radio chemotherapy (oxaliplatin and capecitabine) given concommitant with radiotherapy in patients with gastrointestinal tumors. The trial consists ot two separate studies; CORGI-U in patients with stomach- bile ducts- gallbladder and pancreas cancer, and CORGI-L in patients with colorectal cancer.

CORGI-U will be designed as a phase-I-II-study,in which the first part will be a chemotherapy dose finding study, followed by a phase II part to establish response rates. All subjects receives radiotherapy concommitant.

CORGI-L is a phase II trial, in which patients are treated with chemotherapy at fixed doses with radiotherapy concommitant.

Detailed Description

Not available

Study Timeline

• Study Start: 2003-06
• Primary Completion: 2007-07
• Study Completion: 2009-07
• Study First Submitted: 2009-11-18
• Study First Submitted QC: 2009-11-18
• Study First Posted: 2009-11-19
• Status Verified: 2011-10
• Last Update Submitted: 2011-10-14
• Last Update Posted: 2011-10-17

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 106

Inclusion Criteria

• Over 18 years of age
• Measurable disease according to RECIST
• ECOG Performance Status 0-1
• ANC over 1.5 x 10 9/L
• Platelets over 100 x 10 9/L
• Creatinine less than 1.5 x ULN
• Bilirubin less than 1.5 x ULN
• ALT less than 2.5 x ULN
• Signed informed concent

Exclusion Criteria

• Prior radiotherapy to the same local
• Prior chemotherapy for locally advanced or metastatic disease
• Pregnancy or breast feeding
• Peripheral neuropathy more than grade 1
• Uncontrolled diarrhéa
• Other serious uncontrolled concomitant illness
• Lymph node metastasis that can not be included in the GTV (gross tumor volume), without exceeding the stipulated radiotherapy doses in organs at risk

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Chemoradiotherapy	oxaliplatin, capecitabine, radiotherapy	-

Trial Locations

Locations (5)

Karolinska University Hospital; 🇸🇪 Stockholm, Sweden

Akademiska Sjukhuset; 🇸🇪 Uppsala, Sweden

Centralsjukhuset, Dept of Oncology; 🇸🇪 Karlstad, Sweden

University Hospital Malmö, Dept of Oncology; 🇸🇪 Malmö, Sweden

University Hospital Lund; 🇸🇪 Lund, Sweden