Background. SCLC relapsing or refractory after induction chemotherapy
is a chemoresistant tumor. The outcome of salvage chemotherapy is poor
, with low response rates (< 30%) and short survival times (3-4 months
). The development of drug resistance is considered the major cause of
failure of treatment. VM-26 is one of the most active drugs in SCLC.
Lonidamine has shown to enhance in both vivo and vitro antitumor activ
ity of several cytotoxic drugs acting on drug resistance mechanisms. M
aterials and methods: VM-26 and lonidamine were employed as salvage ch
emotherapy in 30 small cell hmg cancer patients. The doses of chemothe
rapy used were: VM-26 100 mg/m(2), i.v., days I to 3; lonidamine 600 m
g, p.o., days I to 5, recycled every 3 weeks. Results: We observed 13.
3% of objective response and a median survival of 4 months. All the re
sponses were obtained inpatients relapsing after a response to inducti
on chemotherapy. Toxicity was moderate with no toxic death. Conclusion
s: our study shows that Lonidamine failed to increase the VM-26 activi
ty in pretreated small cell lung cancer patients.