Clinical Trials Directory

Trials / Completed

CompletedNCT00376844

External-Beam Radiation Therapy Compared With Vaginal Brachytherapy After Surgery for Stage I Endometrial Cancer

PORTEC-2, Postoperative Radiation Therapy for Endometrial Carcinoma - A Multicenter Randomised Phase III Trial Comparing External Beam Radiation and Vaginal Brachytherapy

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
427 (actual)
Sponsor
Leiden University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: External-beam radiation therapy uses high-energy x-rays to kill tumor cells. Implant radiation therapy uses radioactive material placed directly into or near a tumor to kill tumor cells. Giving external-beam radiation therapy or implant radiation therapy after surgery may kill any tumor cells that remain after surgery. Sometimes, after surgery, the tumor may not need more treatment until it progresses. In this case, observation may be sufficient. It is not yet known whether radiation therapy is more effective than observation when given after surgery in treating stage I endometrial cancer. PURPOSE: This randomized phase III trial is studying external-beam radiation therapy or implant radiation therapy to see how well they work compared with observation in treating patients who have undergone surgery for stage I endometrial cancer.

Detailed description

OBJECTIVES: * Compare the rate of 5-year locoregional relapse in patients undergoing external-beam radiotherapy or vaginal brachytherapy vs observation only after surgery for stage I endometrial cancer. * Compare 5-year rate of distant metastases in these patients. * Determine overall survival rate in these patients. * Determine prognostic factors for relapse and morbidity. OUTLINE: This is a randomized, multicenter study. Patients are randomized to 1 of 2 treatment arms. * Arm I: Patients undergo either vaginal brachytherapy or external-beam radiotherapy. * Arm II: Patients are observed and undergo no further treatment. After completion of study treatment, patients are followed for approximately 83 days. PROJECTED ACCRUAL: A total of 400 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
RADIATIONExternal Beam Radiation Therapy
RADIATIONVaginal Brachytherapy

Timeline

Start date
2002-05-01
Primary completion
2009-05-01
Completion
2016-04-01
First posted
2006-09-15
Last updated
2022-04-12

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00376844. Inclusion in this directory is not an endorsement.