Ame. Bos et al., Pharmacokinetics of MEN-10755, a novel anthracycline disaccharide analogue, in two phase I studies in adults with advanced solid tumours, CANC CHEMOT, 48(5), 2001, pp. 361-369
The doxorubicin analogue MEN-10755 has been identified as a compound with p
romising antitumour activity based on structure-activity studies of a new s
eries of anthracycline disaccharides. The high antitumour activity of MEN-1
0755 in human tumour xenografts, including doxorubicin-resistant xenografts
, and its unique pharmacological and biological properties made this novel
disaccharide analogue an interesting candidate for clinical evaluation. Two
pharmacokinetic phase I studies with different dosing schedules were perfo
rmed in adults with solid refractory malignancies. The pharmacokinetics of
MEN-10755 were studied after a 15-min i.v. infusion given once every 3 week
s or once every week for 3 weeks followed by I week rest. Plasma and urine
levels of MEN-10755 were measured by HPLC with fluorescent detection. It wa
s possible to combine the pharmacokinetic results of the two studies becaus
e there was no accumulation of MEN-10755 before the next infusion of MEN-10
755 in the weekly study with I week rest. The administered dose levels on d
ay I in this study were all in the lower range from the 3-weekly study. The
postinfusion plasma kinetics of MEN-10755 were best described by a triexpo
nential model. The plasma peak levels (C-max) of MEN-10755 showed a linear
relationship with the administered dose. Peak plasma MEN-10755 levels range
d between 474 and 21,587 mug/l. The mean elimination half-life (T-1/2 gamma
) was 20.7 +/- 9.0 h. The AUC(0-infinity) was proportional to the administe
red dose. The mean plasma clearance of MEN-10755 was 6.0 +/- 2.2 1/h per m(
2) with a mean volume of distribution (V-ss) of 95.6 +/- 43.4 1/m(2). The m
ean renal excretion of unchanged drug within 24 h was 4.3 +/- 1.8 %. Compar
ed to epirubicin and doxorubicin, the pharmacokinetics of MEN-10755 were ch
aracterized by an approximately twofold shorter terminal half-life, a much
lower total plasma clearance and a much smaller volume of distribution.