The influence of
tumor temperature (28, 32, 37, 39, 41, or 43 degrees C for 1 h) on the therapeutic efficacy of i.v. single bolus
injections of
ifosfamide (IFO) (32, 65, 125, or 250 mg/kg
body weight) in human
tumor xenografts (MX1
breast carcinoma) grown in nude mice (n = 240) was studied.
Tumor temperature was controlled by water bath immersion. Sixty days
after treatment the percentage of
tumor-free survival was determined. For example, at 37 degrees C IFO in a dose of 65 mg/kg
body weight led to 10%
tumor-free survival in the treated animals. At 43 degrees C the same dose resulted in 60%
tumor-free survival. A clear
drug dose- and temperature-dependent increase of the therapeutic efficacy of an active oxazaphosphorine compound was also demonstrated in vitro. The concentrations of IFO and of
4-hydroxyifosfamide in blood and
tumors at different body temperatures (controlled by water bath immersion) were determined over 120 min and WBC counts were obtained. The half-lives and the areas under the curve for IFO in blood were not significantly different at 37 degrees C and 41 degrees C. Since the half-life of IFO depends mainly on hepatic metabolism, the similarity of half-lives and of areas under the curve for IFO at 37 degrees C and 41 degrees C indicates a constant activation rate. However, significantly lower plasma concentrations of the activated
drug at a liver (body) temperature of 41 degrees C, compared with 37 degrees C, were found, indicating a higher elimination rate. The concentration of the activated
drug in the
tumors within the initial 60 min at 41 degrees C, however, exceeded by > 2-fold that at 37 degrees C. The bone marrow toxicity of the same
drug dose did not significantly increase with body temperature.