Cisplatin toxicity could be decreased by adjusting its dosage to each
patient. For this purpose, a limited sampling method was established a
nd validated based on a Bayesian approach taken using the values of as
says during a 5-day continuous infusion of cisplatin. Using this metho
d, a dosing model to achieve a target plasma concentration of total pl
atinum (Pt) was evaluated retrospectively; the calculated dose of cisp
latin was 95.0 to 104.8% of the actual dose. This model was then studi
ed prospectively and the actual plasma Pt concentration reached at the
end of the infusion was 94.9% of the target concentration A strong co
rrelation was observed between the clearance of Pt and the calculated
clearance of creatinine or Cockroft index (p = 1.7 x 10(-11)), and thi
s correlation was used to develop another cisplatin dosing model. With
this model the actual concentration reached at the end of the infusio
n was 85.3% of the theoretical concentration. The Bayesian approach ga
ve reliable results for most clinical uses, whereas the creatinine bas
ed model has to be improved.