Clinical Trials Directory

Trials / Completed

CompletedNCT00104689

Capecitabine and Oxaliplatin in Treating Older Patients With Metastatic Colorectal Cancer

Phase II Trial Assessing the Impact on the Activity of Daily Living of an Oral Chemotherapy by Capecitabine Associated With an Intravenous Chemotherapy by Oxaliplatin as First Line Treatment of Metastatic Colorectal Adenocarcinoma of Patients Aged Over 70

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
UNICANCER · Academic / Other
Sex
All
Age
70 Years – 120 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: 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. PURPOSE: This phase II trial is studying how well giving capecitabine together with oxaliplatin works in treating older patients with metastatic colorectal cancer.

Detailed description

OBJECTIVES: Primary * Determine the efficacy of capecitabine and oxaliplatin as first-line treatment, as defined by stabilization or improvement by 1 point on Katz's Activities of Daily Living scale, in older patients with metastatic colorectal adenocarcinoma. Secondary * Determine the toxicity of this regimen in these patients. * Determine the percentage of patients who receive the first 3 courses of this regimen (at lower doses) and the percentage of patients who receive all 6 courses of this regimen (at both lower and higher doses). * Determine efficacy of this regimen, as defined by RECIST criteria, in these patients. * Determine the pharmacokinetics of this regimen in these patients. OUTLINE: This is a multicenter, open-label, nonrandomized study. Patients receive oral capecitabine\* once daily on days 1-14 and oxaliplatin\* IV on day 1. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity. NOTE: \*The doses of both capecitabine and oxaliplatin are increased in courses 4-6 in the absence of unacceptable toxicity PROJECTED ACCRUAL: A total of 60 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGcapecitabine
DRUGoxaliplatin

Timeline

Start date
2003-06-30
Primary completion
2007-03-31
Completion
2008-01-01
First posted
2005-03-04
Last updated
2021-02-21

Locations

9 sites across 1 country: France

Source: ClinicalTrials.gov record NCT00104689. Inclusion in this directory is not an endorsement.