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   <subfield code="a">Docetaxel plus epirubicin is a highly active, well-tolerated, first-line chemotherapy for metastatic breast cancer: results of a large, multicentre phase II study</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Serafín Morales, Antonio Lorenzo, Manuel Ramos, Pedro Ballesteros, Miguel Méndez, Concepción Almanza, Javier Castellanos, José Moreno-Nogueira, Joaquín Casal, José Lizón, Amparo Oltra, Adolfo Frau, Ignacio Machengs, Antonio Galán, Joaquín Belón, Cristina Llorca]</subfield>
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   <subfield code="a">Purpose: In this multicentre phase II study, the efficacy and safety profile of the combination of docetaxel and epirubicin as first-line chemotherapy for metastatic breast cancer (MBC) were evaluated.Methods: Epirubicin (75 mg/m2) and docetaxel (75 mg/m2) were given intravenously once every 3 weeks for six cycles to 133 patients with MBC.Results: The overall clinical response rate was 67% (complete and partial responses were 23% and 44%, respectively). The median time to progression was 10.8 months (95% CI 9.7-12.6) and the median overall survival was 19.5 months. Granulocyte colony-stimulating factor support was administered to 32% of patients and in 22% of cycles. Grade 3/4 neutropenia occurred in 35% of patients and febrile neutropenia in 19%. The most frequent grade 3/4 nonhaematological toxicities (as percent of patients) were asthenia (6%), vomiting (5%) and nausea (5%). No patients developed congestive heart failure.Conclusions: The combination of docetaxed and epirubicin was highly active as first-line treatment for MBC and showed a manageable toxicity profile.</subfield>
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   <subfield code="a">Morales</subfield>
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   <subfield code="u">Hospital Puerto Real, Cádiz, Spain</subfield>
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   <subfield code="a">Ramos</subfield>
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   <subfield code="a">Ballesteros</subfield>
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   <subfield code="u">Hospital La Inmaculada, Almería, Spain</subfield>
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