We have conducted a study of ilmofosine (1-hexadecylthio; 2-methoxyeth
yl-rac-glycero-3-phosphocholine) in non-small cell bronchogenic carcin
oma, using a schedule of continuous infusion for 5 days and a dose of
300 mg/m(2)/day. Toxicities were gastrointestinal (nausea, vomiting, d
iarrhea), fatigue and liver function abnormalities. These were severe
and resulted in the removal of some patients from study. No consistent
pattern of bone mallow suppression was seen. No tumor regressions occ
urred in 14 evaluable patients including 5 with no prior therapy. We c
onclude that ilmofosine is inactive in this tumor at this dose and sch
edule.