Cicaprost, a stable prostacyclin analogue with antimetastatic potentia
l, was investigated as regards its effect on the tumor inhibitory pote
ntial of cytostatic drugs exhibiting different modes of action in the
MXT-OVEX mouse mammary carcinoma. Cicaprost itself in doses of 0. 5 mg
/Kg and 1.0 mg/Kg po. daily had no effect on the growth of the sc. -im
planted tumor cis-Platinum at a dose of 1.5 mg/Kg sc. strongly inhibit
ed tumor growth, while at a dose of 0. 75 mg/Kg only a weak effect was
seen. The efficacy of both treatments was not altered by cicaprost (0
.5 mg/Kg; po.) administered in two different schedules. Whereas cyclop
hosphamide (400 mg/Kg; sc.) completely inhibited the growth of the MXT
-OVEX tumor, doxorubicin (2.5 mg/Kg; sc.) and 5-FU (10 mg/Kg; sc.) had
only a weak effect. The combination of cicaprost with either cyclopho
sphamide, doxorubicin or 5-FU did not alter the inhibition of tumor gr
owth. On the basis of these data, we anticipate that the antimetastati
c agent cicaprost can be used in combination with cytostatic regimens
without interfering with their clinical effectiveness.