NRG-BR003
Closed to Accrual
Protocol Information
A Randomized Phase III Trial of Adjuvant Therapy Comparing Doxorubicin Plus Cyclophosphamide Followed by Weekly Paclitaxel with or Without Carboplatin for Node-Positive or High-Risk Node-Negative Triple-Negative Invasive Breast Cancer
Principal Investigator
Vicente Valero
Status
Closed to Accrual
Open to Accrual
June 26, 2015
Closed to Accrual
April 22, 2022
Disease Site
Breast [BR] Breast
Phase
III
Developmental Therapeutics
No
Primary Objective
To determine whether the addition of carboplatin to an adjuvant chemotherapy regimen of doxorubicin/cyclophosphamide followed by paclitaxel will improve the invasive disease-free survival (IDFS) compared to doxorubicin/cyclophosphamide followed by paclitaxel when administered to patients with operable node-positive or high-risk node-negative triple-negative breast cancer.
Patient Population
Patients with operable node-positive or high-risk node-negative triple-negative breast cancer who have undergone either a mastectomy or lumpectomy.
Target Accrual
990
Protocol Documents
Available via the National Cancer Institute (NCI) Cancer Trials Support Unit (CTSU) website.