Randomized Phase III Trial With Docetaxel Plus Epirubicine Versus Docetaxel Plus Capecitabine for Metastatic Breast Cancer

Hellenic Oncology Research Group

Status and phase

Completed

Phase 3

Conditions

Breast Cancer

Treatments

Drug: Capecitabine

Drug: Docetaxel

Drug: Epirubicin

Study type

Interventional

Funder types

Other

Identifiers

NCT00429871

CT/02.09

Details and patient eligibility

About

The combination of docetaxel+epirubicin is highly effective and well tolerated as first line treatment in patients with metastatic breast cancer (MBC). Capecitabine is an active drug in women with MBC pretreated with taxane and anthracycline. Docetaxel increases the intracellular levels of thymidilate phosphorylase and thus is synergistic with capecitabine. The combination of docetaxel plus capecitabine is highly active and superior to docetaxel monotherapy in women with MBC pretreated with an anthracycline

Full description

This trial will compare the efficacy of docetaxel plus epirubicin versus docetaxel plus capecitabine combinations as first line treatment in women with MBC

Enrollment

272 patients

Sex

Female

Ages

19 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Histologically- or cytologically- confirmed metastatic breast adenocarcinoma.
No previous chemotherapy treatment for metastatic disease.
No previous anthracycline treatment except as adjuvant therapy at least one year before.
Age 19-75 years old
Presence of measurable disease
Performance status 0-2 (WHO)
Adequate cardiac function (LVEF >50%) without a recent (within 6 months) history of myocardial infraction and/or unstable or uncontrolled angina.
Adequate bone marrow(absolute neutrophil count >1500/mm3, platelet count >100.000/mm3, hemoglobin >10gr/mm3), liver (bilirubin <1.5 times upper limit of normal and SGOT/SGPT <2 times upper limit of normal) and renal function (creatinine <2mg/dl).
No previous radiotherapy to more than 25% of marrow-containing bones.
Written informed consent

Exclusion criteria

Active brain metastases.
Psychiatric illness or social situation that would preclude study compliance
Other concurrent uncontrolled illness.
Other invasive malignancy within the past 5 years except of nonmelanoma skin cancer.
Positive pregnancy for premenopausal women.
Concurrent antineoplastic treatment e.g. hormonal therapy