Clinical Trials Directory

Trials / Completed

CompletedNCT00156312

Evaluation of Tumor Factors in Breast Cancer Treated With Docetaxel and Capecitabine

Evaluation of Thymidine Phosphorylase and Other Predictive/Prognostic Factors in Primary Breast Cancer Treated With Docetaxel and Capecitabine (DC)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
25 (estimated)
Sponsor
University of Michigan Rogel Cancer Center · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether the combination of the drugs docetaxel and capecitabine is effective in treating breast cancer patients.

Detailed description

Some chemotherapy drugs are thought to work in synergy, meaning they work better in combination, rather than singly because one drug may cause changes in the tumor that will make the other drug more effective. The drugs docetaxel and capecitabine may work in synergy, based on laboratory studies in tumors. These laboratory studies show that docetaxel increases the levels of a critical enzyme, called thymidine phosphorylase (TP), which is necessary to activate the capecitabine. This study will use this promising chemotherapy combination in patients with breast cancer. Before, during, and after chemotherapy, the participants' breast tumors will be examined to see if TP increases, as predicted by the laboratory studies. The study will also look at other factors in tumors and blood that may be able to predict how effective the chemotherapy will be for each individual, so that in the future we may better select the best chemotherapy for an individual's cancer.

Conditions

Interventions

TypeNameDescription
DRUGDocetaxel
DRUGCapecitabine

Timeline

Start date
2003-07-01
Primary completion
2005-05-01
Completion
2007-02-01
First posted
2005-09-12
Last updated
2012-02-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00156312. Inclusion in this directory is not an endorsement.