Phase I study of BW12C in combination with mitomycin C in patients with advanced gastrointestinal cancer.

Ramsay, J R; Bleehen, N M; Dennis, I; Workman, P; Ward, R; Falk, S J; Bedford, P; Wootton, R et al. · Int J Radiat Oncol Biol Phys · 1992

Level II

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Abstract

The effect of combining the oxyhemoglobin-modifying drug BW12C with mitomycin C was investigated in a Phase I study of 18 patients with advanced gastrointestinal cancer. The dose of BW12C was increased from 20 mg/kg to 50 mg/kg to modify the hemoglobin-oxygen saturation curve by up to 48%. The period of maximum modification was then prolonged for up to 3 hr by a maintenance infusion of 4-6 mg/kg/hr. Pharmacokinetics of BW12C and mitomycin C were performed in all patients. Peak levels of BW12C increased from 139 micrograms/ml to 378 micrograms/ml. Plasma half life was independent of dose, with an average of 3.3 hr. BW12C was well tolerated with no severe side effects. Three patients had objective tumour responses.

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