Epirubicin and Docetaxel Combination (ET) or Epirubicin Followed by Docetaxel (E/T) for Node Negative (N0) High Risk Breast Cancer Patients

PHASE3CompletedINTERVENTIONAL
Enrollment

658

Participants

Timeline

Start Date

June 30, 2001

Primary Completion Date

August 31, 2013

Study Completion Date

August 31, 2013

Conditions
Breast Cancer
Interventions
DRUG

Docetaxel

Docetaxel at the dose of 75 mg/m2 intravenously (IV) every 3 weeks for 4 consecutive cycles

DRUG

Epirubicin

Epirubicin at the dose of 90 mg/m2 IV every 3 weeks for 4 consecutive cycles

DRUG

Epirubicin

Epirubicin at the dose of 75 mg/m2 IV every 3 weeks for 6 consecutive cycles

DRUG

Docetaxel

Docetaxel at the dose of 75 mg/m2 IV every 3 weeks for 6 consecutive cycles

Trial Locations (12)

71110

University Hospital of Heraklion, Heraklion

Unknown

University Hospital of Alexandroupolis Dept. of Medical Oncology, Alexandroupoli

"Agios Savvas Anticancer Hospital of Athens", Athens

"IASO General Hospital of Athens", Athens

"Laikon General Hospital", Athens

"Marika Iliadis Hospital of Athens", Athens

"Metaxa's Anticancer Hospital of Pireas", Athens

401 Military Hospital of Athens, Athens

Air Forces Military Hospital of Athens, Athens

State General Hospital of Larissa, Larissa

"AXEPA General Hospital of Thessaloniki", Thessaloniki

"Theagenion Anticancer Hospital of Thessaloniki", Thessaloniki

All Listed Sponsors
collaborator

University Hospital of Crete

OTHER

lead

Hellenic Oncology Research Group

OTHER