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. 2015 Nov 24;18(2):362–371. doi: 10.1208/s12248-015-9838-1

Table III.

Parameter Estimates for Pharmacokinetic-Pharmacodynamic Model. A, Parameters Estimated by Control, RTV and DOC Groups; B, Parameter Estimated by Control, RTV, DOC and DOC+RTV Groups

A B
Control, RTV, DOC groups Control, RTV, DOC, DOC+RTV groups
Parameters Units Estimate RSE (%) Shrinkage (%) Estimate RSE (%) Shrinkage (%)
Population parameter
 Baseline tumour volume (BASE) mm3 214 3.1 211 1.4
 Net tumour growth rate in untreated groups (Kg0) /week 1.18 5.7 1.32 3.4
 Progression appearance factor (LAMBDA) /week 0.11 16.0 0.061 10.1
 Cell transition rate by docetaxel to effect compartment (KKDOC) /week 1.81 4.6 1.90 2.1
 Cell elimination rate by docetaxel from effect compartment (KKeDOC) /week 2.93 18.2 4.62 10.1
 Docetaxel tumour concentration with 50% of maximum anti-cancer effect (EC50DOC) ng/g 96.5 62.9 310 15.0
 Cell transition rate by ritonavir to effect compartment (KKRTV) /week 0.0054 17.4
 Cell elimination rate by ritonavir from effect compartment (KKeRTV) /week 7.45 4.6
Between-subject variability
 Baseline tumour volume (BASE) CV% 22.5 10.5 7.9 21.4 7.0 9.1
Residual unexplained variability
 Proportional residual error on tumour volumes CV% 23.0 10.0 3.4 24.8 8.7 2.8

CV coefficient of variation, DOC docetaxel, RSE relative standard error, RTV ritonavir