Radiation Therapy (WBI Versus PBI) in Treating Women Who Have Undergone Surgery For Ductal Carcinoma In Situ or Stage I or Stage II Breast Cancer

NCT00103181 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 4216

Last updated 2022-04-14

No results posted yet for this study

Summary

RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Giving radiation therapy in different ways may kill any tumor cells that remain after surgery. It is not yet known whether whole breast radiation therapy is more effective than partial breast radiation therapy in treating breast cancer.

PURPOSE: This randomized phase III trial is studying whole breast radiation therapy to see how well it works compared to partial breast radiation therapy in treating women who have undergone surgery for ductal carcinoma in situ or stage I or stage II breast cancer.

Conditions

Interventions

RADIATION

3-dimensional conformal accelerated partial breast irradiation

RADIATION

brachytherapy

RADIATION

whole breast irradiation

Patients undergo radiation therapy once daily (days 1-5) for up to 7 weeks

RADIATION

MammoSite or other single-entry intracavitary device

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Radiation Therapy Oncology Group

    collaborator NETWORK
  • SWOG Cancer Research Network

    collaborator NETWORK
  • NSABP Foundation Inc

    lead NETWORK

Principal Investigators

  • Norman Wolmark, MD · NSABP Foundation Inc

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-03-31
Primary Completion
2018-08-31
Completion
2018-08-31

Countries

  • United States
  • Canada
  • Ireland
  • Israel

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00103181 on ClinicalTrials.gov