TY - JOUR
T1 - Flat dosing of carboplatin is justified in adult patients with normal renal function
AU - Ekhart, Corine
AU - De Jonge, Milly E.
AU - Huitema, Alwin D.R.
AU - Schellens, Jan H.M.
AU - Rodenhuis, Sjoerd
AU - Beijnen, Jos H.
PY - 2006/11/1
Y1 - 2006/11/1
N2 - Purpose: The Calvert formula is a widely applied algorithm for the a priori dosing of carboplatin based on patients glomerular filtration rate (GFR) as accurately measured using the 51Cr-EDTA clearance. Substitution of the GFR in this formula by an estimate of creatinine clearance or GFR as calculated by formulae using serum creatinine (SCR; Cockcroft-Gault, Jelliffe, and Wright) is, however, routine clinical practice in many hospitals. The goal of this study was to validate this practice retrospectively in a large heterogeneous adult patient population. Experimental Design: Concentration-time data of ultrafilterable platinum of 178 patients (280 courses, 3,119 samples) with different types of cancer receiving carboplatin-based chemotherapy in conventional and high doses were available. Data were described with a linear two-compartment population pharmacokinetic model. Relations between S CR-based formulae for estimating renal function and carboplatin clearance were investigated. Results: None of the tested SCR-based estimates of renal function were relevantly related to the pharmacokinetic variables of carboplatin. Neither SCR (median, 51; range, 18-124 μmol/L) nor the estimated GFR using the three different formulae was related to carboplatin clearance. Conclusions: Our data do not support the application of modifications of the Calvert formula by estimating GFR from SCR in the a priori dosing of carboplatin in patients with relatively normal renal function (creatinine clearance, >50 mL/min). For targeted carboplatin exposures, the original Calvert formula, measuring GFR using the 51Cr-EDTA clearance, remains the method of choice. Alternatively, in patients with normal renal function, a flat dose based on the mean population carboplatin clearance should be administered.
AB - Purpose: The Calvert formula is a widely applied algorithm for the a priori dosing of carboplatin based on patients glomerular filtration rate (GFR) as accurately measured using the 51Cr-EDTA clearance. Substitution of the GFR in this formula by an estimate of creatinine clearance or GFR as calculated by formulae using serum creatinine (SCR; Cockcroft-Gault, Jelliffe, and Wright) is, however, routine clinical practice in many hospitals. The goal of this study was to validate this practice retrospectively in a large heterogeneous adult patient population. Experimental Design: Concentration-time data of ultrafilterable platinum of 178 patients (280 courses, 3,119 samples) with different types of cancer receiving carboplatin-based chemotherapy in conventional and high doses were available. Data were described with a linear two-compartment population pharmacokinetic model. Relations between S CR-based formulae for estimating renal function and carboplatin clearance were investigated. Results: None of the tested SCR-based estimates of renal function were relevantly related to the pharmacokinetic variables of carboplatin. Neither SCR (median, 51; range, 18-124 μmol/L) nor the estimated GFR using the three different formulae was related to carboplatin clearance. Conclusions: Our data do not support the application of modifications of the Calvert formula by estimating GFR from SCR in the a priori dosing of carboplatin in patients with relatively normal renal function (creatinine clearance, >50 mL/min). For targeted carboplatin exposures, the original Calvert formula, measuring GFR using the 51Cr-EDTA clearance, remains the method of choice. Alternatively, in patients with normal renal function, a flat dose based on the mean population carboplatin clearance should be administered.
UR - http://www.scopus.com/inward/record.url?scp=33751305679&partnerID=8YFLogxK
U2 - 10.1158/1078-0432.CCR-05-1076
DO - 10.1158/1078-0432.CCR-05-1076
M3 - Article
C2 - 17085665
AN - SCOPUS:33751305679
SN - 1078-0432
VL - 12
SP - 6502
EP - 6508
JO - Clinical Cancer Research
JF - Clinical Cancer Research
IS - 21
ER -