Clinical Trials Directory

Trials / Completed

CompletedNCT00276796

Paclitaxel, Topotecan, and Cisplatin in Treating Patients With Advanced, Persistent, or Recurrent Cervical Cancer

A Limited Access Phase II Trial of Weekly Topotecan (NSC #609699), Paclitaxel (NSC #673089), and Cisplatin (NSC #119875) in the Treatment of Advanced, Persistent, or Recurrent Carcinoma of the Cervix

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Gynecologic Oncology Group · Network
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as paclitaxel, topotecan, and cisplatin, 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. PURPOSE: This phase II trial is studying how well giving paclitaxel together with topotecan and cisplatin works in treating patients with advanced, persistent, or recurrent cervical cancer.

Detailed description

OBJECTIVES: Primary * Estimate the antitumor activity of the combination of paclitaxel, topotecan, and cisplatin in patients with advanced, persistent, or recurrent carcinoma of the cervix. * Determine the nature and degree of toxicity for this drug regimen in these patients. Secondary * Determine the duration of progression-free survival and overall survival. * Determine the impact of prior chemoradiation on response to treatment. OUTLINE: This is an open-label study. Patients receive paclitaxel IV over 1 hour followed by topotecan IV over 30 minutes and cisplatin IV over 1 hour on days 1 and 8. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed periodically for 5 years. PROJECTED ACCRUAL: A total of 66 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGcisplatin
DRUGpaclitaxel
DRUGtopotecan hydrochloride

Timeline

Primary completion
2007-01-01
First posted
2006-01-13
Last updated
2013-05-27

Source: ClinicalTrials.gov record NCT00276796. Inclusion in this directory is not an endorsement.