Encouraging results with Paclitaxel are reported in ovarian cancer pat
ients relapsing and progressing after platinum-based chemotherapy; how
ever, the two populations have different probabilities of a response t
o a second-line treatment. Here we report the results achieved in 39 p
atients with platinum-refractory ovarian cancer, treated with Paclitax
el 175 mg/qm(2) (or 135 mg/m(2) if heavily pretreated) using 3-hour in
travenous infusion every 3 weeks, in an attempt to verify the activity
of this drug in platinum-resistant patients. The toxicity was mild to
moderate and primarily hematologic and neurologic. The objective resp
onse rate is 12.8% with no complete responses. The response duration w
as brief and the median survival 6 (range 1-17) months. An accurate co
st-benefit balance is necessary before routinely use of Paclitaxel in
platinum-refractory patients. Further research is needed to determine
the optimal role of Paclitaxel in the whole therapeutic strategy for o
varian cancer.