EPIRUBICIN IN ADVANCED ENDOMETRIAL ADENOCARCINOMA - A PHASE-II STUDY OF THE GRUPO-GINECOLOGICO-ESPANOL-PARA-EL-TRATAMIENTO-ONCOLOGICO (GGETO)

27 patients with FIGO stage III-IV endometrial adenocarcinoma were entered in a phase II trial evaluating activity and safety of epirubicin given at 80 mg/m2 intravenously every 3 weeks. 2 complete remissions (including a pathological one) and 5 partial responses were observed for a response rate of 26% (95% confidence interval 11-46). The median time to progression and median survival for all treated patients was 6 and 9.5 months, respectively. Treatment was well tolerated. Haematological toxicity was mild. The median total cumulative dose of epirubicin was 480 mg/m2 (160-880) and cardiac toxicity was not observed. Further studies with higher doses of epirubicin in combination with other active drugs are indicated.