The optimal schedule for the administration of 5-fluorouracil (5-FU) i
n the management of advanced colorectal cancer remains to be determine
d. It has been suggested that this drug may be given by the subcutaneo
us route and that following a short infusion the bioavailability is si
milar to that observed after intravenous administration. We report the
results we obtained in a patient treated with an intravenous bolus of
5-FU followed by a 22-h subcutaneous infusion. In this patient the bi
oavailability of 5-FU given by subcutaneous infusion was 0.94. The ste
ady-state plasma levels of 5-FU reached during subcutaneous infusion w
ere comparable with those achieved during intravenous infusion. Follow
ing four cycles of subcutaneous therapy, painless blistering was noted
at the infusion sites, which healed following the cessation of subcut
aneous therapy. Further studies are required to evaluate this route of
therapy as an alternative to protracted intravenous therapy. The main
dose-limiting side effect appears to be local skin toxicity.