Summary Infusional 5-fluorouracil (F) with cisplatin (C) and epirubicin (E), so- (Smith et al., 1995). The schedule has also shown high activity in the treatment of advanced gastric carcinoma with a response rate of 71% (Findlay et al., 1994).The underlying rationale for this schedule is as follows: Phase I studies have demonstrated that 5-FU can be administered by protracted continuous infusion at a dose of 300 mg m-2 day-' without interruption for up to 60 days or up to 36 g cumulative dose (Lokich et al., 1981); response rates of up to 53% have been reported in patients with metastatic breast cancer extensively pretreated with chemotherapy (Huan et al., 1989). This represents a more than 3-fold increase in response compared with conventional studies. In an overview of six phase II studies involving 182 patients with refractory breast cancer, most of whom were pretreated with bolus 5-FU, an average response rate of 29% (range 17-53%) has been reported (Hansen, 1991). As originally suggested in the phase I study by Lokich and subsequently confirmed by phase II studies, myelosuppression, an important toxic effect occurring with bolus administration, is rarely reported with infusional 5-FU and the dose-limiting toxicities are stomatitis, diarrhoea and plantar-palmar erythema (Lokich et al