Gemcitabine is a new nucleoside antimetabolite with established activity ag
ainst solid tumours. In previously treated patients the response rate with
the drug alone was around 13%. Combination therapy with gemcitabine-cisplat
in or gemcitabine-paclitaxel induced responses in 53 and 40% respectively.
In previously untreated patients with poor prognostic features a 24% respon
se rate was reported for the drug alone, but in combination with cisplatin
remissions were found in 53%-71% of patients.
Gemcitabine, paclitaxel, and carboplatin (or cisplatin) in combination appe
ared to be a feasible and active combination. In a pilot with eight previou
sly treated patients all obtained a remission and in untreated patients a r
emission occurred in all evaluable patients either clinically or measured b
y a decrease of CA 125. Dose-limiting toxicity is mainly haematological.