TY - JOUR
T1 - The effect of different doses of cyclosporin A on the systemic exposure of orally administered paclitaxel
AU - Malingré, M M
AU - Beijnen, J H
AU - Rosing, H
AU - Koopman, F J
AU - van Tellingen, O
AU - Duchin, K
AU - ten Bokkel Huinink, W W
AU - Swart, M
AU - Lieverst, J
AU - Schellens, J H
PY - 2001/4
Y1 - 2001/4
N2 - The objective of this study was to define the minimally effective dose of cyclosporin A (CsA) that would result in a maximal increase of the systemic exposure to oral paclitaxel. Six evaluable patients participated in this randomized cross-over study in which they received at two occasions two doses of 90 mg/m(2) oral paclitaxel 7 h apart in combination with 10 or 5 mg/kg CsA. Dose reduction of CsA from 10 to 5 mg/kg resulted in a statistically significant decrease in the area under the plasma concentration-time curve (AUC) and time above the threshold concentrations of 0.1 microM (T>0.1 microM) of oral paclitaxel. The mean (+/-SD) AUC and T>0.1 microM values of oral paclitaxel with CsA 10 mg/kg were 4.29+/-0.88 microM x h and 12.0+/-2.1 h, respectively. With CsA 5 mg/kg these values were 2.75+/-0.63 microM x h and 7.0+/-2.1 h, respectively (p=0.028 for both parameters). In conclusion, dose reduction of CsA from 10 to 5 mg/kg resulted in a significant decrease in the AUC and T>0.1 microM values of oral paclitaxel. Because CsA 10 mg/kg resulted in similar paclitaxel AUC and T>0.1 microM values compared to CsA 15 mg/kg (data which we have published previously), the minimally effective dose of CsA is determined at 10 mg/kg.
AB - The objective of this study was to define the minimally effective dose of cyclosporin A (CsA) that would result in a maximal increase of the systemic exposure to oral paclitaxel. Six evaluable patients participated in this randomized cross-over study in which they received at two occasions two doses of 90 mg/m(2) oral paclitaxel 7 h apart in combination with 10 or 5 mg/kg CsA. Dose reduction of CsA from 10 to 5 mg/kg resulted in a statistically significant decrease in the area under the plasma concentration-time curve (AUC) and time above the threshold concentrations of 0.1 microM (T>0.1 microM) of oral paclitaxel. The mean (+/-SD) AUC and T>0.1 microM values of oral paclitaxel with CsA 10 mg/kg were 4.29+/-0.88 microM x h and 12.0+/-2.1 h, respectively. With CsA 5 mg/kg these values were 2.75+/-0.63 microM x h and 7.0+/-2.1 h, respectively (p=0.028 for both parameters). In conclusion, dose reduction of CsA from 10 to 5 mg/kg resulted in a significant decrease in the AUC and T>0.1 microM values of oral paclitaxel. Because CsA 10 mg/kg resulted in similar paclitaxel AUC and T>0.1 microM values compared to CsA 15 mg/kg (data which we have published previously), the minimally effective dose of CsA is determined at 10 mg/kg.
KW - Adenocarcinoma/drug therapy
KW - Administration, Oral
KW - Adult
KW - Aged
KW - Antineoplastic Combined Chemotherapy Protocols/pharmacokinetics
KW - Area Under Curve
KW - Breast Neoplasms/drug therapy
KW - Carcinoma, Small Cell/drug therapy
KW - Cyclosporine/administration & dosage
KW - Dose-Response Relationship, Drug
KW - Drug Administration Schedule
KW - Female
KW - Gastrointestinal Diseases/chemically induced
KW - Hematologic Diseases/chemically induced
KW - Humans
KW - Infusions, Intravenous
KW - Lung Neoplasms/drug therapy
KW - Male
KW - Middle Aged
KW - Neoplasms/drug therapy
KW - Paclitaxel/administration & dosage
KW - Premedication
KW - Stomach Neoplasms/drug therapy
KW - Uterine Cervical Neoplasms/drug therapy
KW - Uterine Neoplasms/drug therapy
U2 - 10.1097/00001813-200104000-00008
DO - 10.1097/00001813-200104000-00008
M3 - Article
C2 - 11335792
SN - 0959-4973
VL - 12
SP - 351
EP - 358
JO - Anti-Cancer Drugs
JF - Anti-Cancer Drugs
IS - 4
ER -