Table 3.
Parameter | Unit | Original data estimatea | Bootstrap average | Bootstrap 95 % CIb |
---|---|---|---|---|
CL/Fn | L/h | 20.5 | 20.5 | 17.3–24.6 |
V1/Fn | L | 105 | 107 | 87–136 |
Q/Fn | L/h | 35.8 | 37.3 | 21.5–48.5 |
V2/Fn | L | 450 | 424 | 297–583 |
ka | h−1 | 1.14 | 1.18 | 0.80–1.78 |
ka, study 2 | h−1 | 0.37 | 0.38 | 0.31–0.48 |
Lag time | h | 0.21 | 0.22 | 0.20–0.24 |
Lag timestudy 2 | h | 0.82 | 0.81 | 0.65–0.90 |
Covariates on F | ||||
CYP3A5 *1/*3 | factor | 0.51 | 0.51 | 0.42–0.62 |
Age and sex | ||||
Fminage, females | 0.44 | 0.43 | 0.23–0.60 | |
Fminage, males | 0.68 | 0.66 | 0.36–0.89 | |
Fage50 | years | 44 | 47 | 39–70 |
HillF age | 12.2 | 14.0 | 3.5–24.9 | |
Time, early | ||||
Fmaxearly | 1.87 | 2.04 | 1.60–3.9 | |
Fearly50 | days | 2.6 | 2.5 | 1.7–3.0 |
HillF early | 10.0c | 9.4 | 3.7–10.0c | |
Time, late | ||||
Fmaxlate | 0.27 | 0.28 | 0.14–0.49 | |
Flate50 | days | 30 | 31 | 24–40 |
HillF late | 2.3 | 2.5 | 1.6–4.7 | |
BSV | ||||
CL/Fn | % | 33 | 31 | 21–40 |
V1/Fn | % | 14 | 14 | 0.2–37 |
Q/Fn | % | 91 | 86 | 51–114 |
V2/Fn | % | 52 | 52 | 32–74 |
HillF late | % | 117 | 113 | 78–146 |
Correlation | ||||
CL/Fn ∼ Q/Fn | 0.75 | 0.74 | 0.41–0.92 | |
BOV | ||||
Fn | % | 16 | 16 | 13–18 |
ka | % | 63 | 60 | 41–84 |
Residual variability | ||||
Proportional error | % | 16.7 | 16.7 | 15.2–18.4 |
Study 2 | factor | 0.57 | 0.56 | 0.41–0.72 |
Study 3 | factor | 0.73 | 0.72 | 0.57–0.90 |
CI, Confidence interval, Fn, bioavailability at baseline nadir (5 days after transplantation); CL/Fn, apparent clearance; V1/Fn, apparent central volume of distribution; Q/Fn, apparent intercompartmental clearance; V2/Fn, apparent peripheral volume of distribution; ka, absorption rate constant; FFM, fat-free mass; Fminage, the minimum value of F at decreasing age relative to reference (male > 60 years); Fage50, the age with half maximum effect on F; HillF age, shape coefficient for the change in F with age; Fmaxearly, the maximum increase in F immediately after transplantation relative to Fn; Fearly50, the day with half maximum early effect on F; HillF early, shape coefficient for the change in F at early time; Fmaxlate, maximum increase in F at later time point, relative to Fn; Flate50, the day with half maximum later effect on F; HillF late, shape coefficient for the change in F at later time; BSV, between subject variability; BOV, between occasion variability
The final model was parameterized as follows: CL/Fn = 20.5 × (FFM /60)3/4 L/h; V1/Fn = 107 × (FFM /60) L; Q/Fn = 37.3 × (FFM /60)3/4 L/h; V2/Fn = 424 × (FFM /60) L
F = [2.04 + (1 − 2.04)/(1 + (TXT/2.5)−9.4)] × [1 + 0.28 / (1+(TXT/31)−2.5)] × [Fminage + (1 − Fminage)/(1 + (AGE/47)−14)] × FCYP where Fminage = 0.43 in females and 0.66 in males, FCYP is 0.51 in CYP3A5 expressers and 1 in CYP3A5 nonexpressers and TXT is the time after transplantation in days
aStandardized to 40-year-old male, CYP3A5 nonexpresser with fat-free mass of 60 kg and hematocrit of 45 %, at a time point with the lowest estimated bioavailability (Fn, day 5 post-transplant)
b2.5–97.5 percentile obtained from 500 bootstrap replicates
cUpper bound