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[Comparison of gemcitabine production costs in individualized and standardized doses]
Mélanie Closset1, Louise Lombet2, Justine Hubert3
1Laboratoire de biologie clinique, avenue Thérasse 1, 5530 Yvoir, Belgique; Drug Stability Research Group, CHU UCL Namur, avenue Thérasse 1, 5530 Yvoir, Belgique; URL7365 - Groupe de recherche sur les formes injectables et les technologies associées (GRITA), CHU de Lille, université de Lille, 59000 Lille, France.
Introduction:
Cancer chemotherapy doses are often adapted to patients' body surface area and produced individually. Alternatively, dose-banding promotes batch production of clinically defined fixed doses, for which a standard deviation of±5% determines a band incorporating individual doses calculated on the basis of body surface area. The aim is to compare the costs of individualized and batch production of gemcitabine in a centralized chemotherapy reconstitution unit.
Method:
The study was carried out using a cost-minimization analysis. The first step was to identify the percentage of gemcitabine preparations eligible for standardization over a one-year period, and to define the standardized doses of clinical interest, taking into account a standard deviation of±5%. The second step was to compare the direct and indirect costs of individualized production with those of mass production.
Results:
The percentage of standardizable preparations was evaluated at 69.8%, with standardized doses of 1500mg±5%, 1600mg±5%, 1800mg±5%, 2000mg±5% and 2200mg±5%. Comparison of production costs for a total of 324 bags over one year showed that dose-banding reduced costs by 7%.
Discussion:
The cost difference between individualized production and batch production of standardized doses of gemcitabine bags is in favor of dose-banding. The analysis could be extended to other anticancer molecules.
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