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British Journal of Clinical Pharmacology logoLink to British Journal of Clinical Pharmacology
. 2003 Oct;56(4):463. doi: 10.1046/j.1365-2125.2003.01976.x

Erratum

PMCID: PMC1884369

Br J Clin Pharmacol 2003; 56 (1); 46–56.

A population pharmacokinetic model for paclitaxel in the presence of a novel P-gp modulator, Zosuquidar (LY335979)

S. Callies, D. P de Alwis, A. Harris, P. Vasey, J. H. Beijnen, J. H. Schellens, M. Burgess & L. Aarons

P. 52. The publisher regrets that Table 3 was printed incorrectly. The correct Table is printed below.

Table 3.

Paclitaxel pharmacokinetic parameters from the basic and covariate (categorical and continous) population pharmacokinetic models.

Basic model Categorical relationship (final model) Continuous relationship
OBJF 8727.003 8703.350 8680.895
Parameters (value (SE%))
CL changing with time*
 Slope (θ2) (lh−2) 9.35 (7.32) 10.0 (7.92) 9.66 (6.95)
 Min CL (θ1) (lh−1) 7.64 (12.2) 8.48 (12.9) 8.59 (29.9)
t504) (h) 8.76 (16.4) 9.36 (28.2) 7.27 (102)
 γ13) 2.94 (23.5) 2.68 (30.2) 2.12 (95.3)
Effect of zosuquidar on paclitaxel CL
 Decrease with LY Cmax>350(µgl−1) (%) 25.2 (12.4)
 Emax (lh−1) 5.49 (43.5)
 LY Cmax50 (µgl−1) 328 (15.4)
 γ2 9.18 (129)
V1 (l) 7.93 (14.0) 7.95 (13.8) 8.38 (13.0)
V2 (l) 198 (7.78) 196 (7.81) 194 (16.0)
Q2 (lh−1) 11.1 (7.37) 10.8 (9.35) 11.2 (11.3)
Q3 (lh−1) 6.57 (15.8) 6.76 (16.4) 6.35 (39.4)
V3(l) 7.00 (15.4) 7.51 (18.9) 10.2 (164)
ω CL (%) 27.2 (33.2) 25.9 (29.7) 24.8 (34.3)
ω CL-Q2 (%) 32.6 (23.4) 30.5 (23.2) 29.6 (24.7)
ω Q2 (%) 44.5 (28.0) 43.7 (26.1) 43.5 (37.0)
ω CL-V2 (%) 29.3 (30.7) 26.1 (38.4) 24.2 (39.5)
ω Q2-V2 (%) 40.7 (29.9) 39.6 (29.2) 37.5 (35.1)
ωV2 (%) 43.7 (26.6) 42.8 (26.0) 40.9 (31.4)
ωV1 (%) 38.5 (58.6) 40.0 (52.4) 41.7 (58.6)
ω IOV CL (%) 20.9 (33.2) 15.2 (53.9) 16.1 (56.2)
ω IOV V1 (%) 57.5 (39.6) 54.5 (42.8) 46.6 (47.9)
Residual variance (%) 22.7 (7.75) 22.9 (7.77) 22.5 (8.00)
*

During the infusion *postinfusion Inline graphic with INF the length of the infusion and time the time from the start of the infusion.


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