Aims: Epirubicin is an analogue of doxorubicin with a similar activity
but less toxicity. The aim of this study was to evaluate the efficacy
and the tolerability of a weekly schedule of epirubicin. Methods: Fif
ty-three patients with metastatic breast cancer, pretreated and/or wit
h a low performance status, were treated with 25 mg/m2/week of the dru
g. Results: Of the 49 evaluable patients, 3 achieved a complete respon
se (6.1 %) and 21 a partial response (42.8 %) with a median duration o
f 6.3 months. Median survival was significantly higher in responders t
han in nonresponders: 15.2 vs 6.0 months (P < 0.005). Furthermore, a m
arked improvement in performance status was observed (ECOG scale). No
cardiologic toxicity was observed, and gastrointestinal toxicity was l
ow. Conclusions. Epirubicin administered weekly represent a valid alte
rnative to conventional treatments.