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Randomized Controlled Trial
. 2007 Mar;63(3):292-9.
doi: 10.1111/j.1365-2125.2006.02757.x. Epub 2006 Aug 30.

Dose selection and population pharmacokinetics of PEG-Intron in patients with chronic myelogenous leukaemia

Samir Gupta  1 , Juif Jen, Karen Kolz, David Cutler
Affiliations
Randomized Controlled Trial

Dose selection and population pharmacokinetics of PEG-Intron in patients with chronic myelogenous leukaemia

Samir Gupta et al. Br J Clin Pharmacol. 2007 Mar.

Abstract

Aims: To assess the dose selection using population pharmacokinetics of Pegylated Intron-alpha2b (PEG-Intron) in patients with chronic myelogenous leukaemia (CML).

Methods: PEG-Intron 3-6 microg kg(-1) was administered subcutaneously once a week and blood samples were collected up to 48 weeks of treatment. A total of 624 samples collected from 137 patients were included in the analysis. Nonlinear mixed-effects modelling was used to analyse the sparsely sampled concentration data from a clinical efficacy trial. Covariates in the analysis included weight, sex, age, race, serum creatinine and estimated creatinine clearance (CLcr).

Results: The apparent clearance of PEG-Intron decreased after repeated dosing. The clearance at treatment week 4 was 42.3 l day(-1) (patients with CLcr 120 ml min(-1)) with interpatient variability 30%. At treatment week 48, the clearance value was reduced to 69% of its week 4 value. CLcr, a composite variable calculated from body weight, sex, age and serum creatinine, had a small but statistically significant influence on the clearance of PEG-Intron. The clearance of PEG-Intron in patients with CML was 40% higher than that of hepatitis C virus-infected patients.

Conclusion: The dose of PEG-Intron 6.0 microg kg(-1) week(-1) appeared appropriate in the treatment of patients with CML.

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Figures

Figure 1
Figure 1
Plots of PEG-Intron immunoassay concentration data (pg ml−1) vs. elapsed time from last dose by treatment week. The broken line is the fitted line generated using population mean parameters
Figure 3
Figure 3
Individual T50 estimates vs. covariates and some clinical and demographic variables
Figure 4
Figure 4
Mean PEG-Intron apparent clearance relative to duration of treatment. The solid line is for the current chronic myelogenous leukaemia trial and the three broken lines are for previous chronic hepatitis C trial [9, 10]. The smooth lines (solid and broken) were obtained using local linear regression (‘loess’ function in S-plus). 6.0 mcg/kg (——–), 0.5 mcg/kg (—), 1.0 mcg/kg (—), 1.5 mcg/kg (—)
Figure 2
Figure 2
Individual CL0 estimates vs. covariates and some demographic and clinical variables
See this image and copyright information in PMC

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References

    1. Faderl S, Talpaz M, Estrov Z, Kantarjian HM. Chronic myelogenous leukemia. Biol Ther Ann Intern Med. 1999;131:207. - PubMed
    1. Kantarjian HM, O’Brien S, Anderlini P, Talpaz M. Treatment of chronic myelogenous leukemia: current status and investigational options. Blood. 1996;87:3069–81. - PubMed
    1. Talpaz M, Kantarjian H, Kurzrock R. Interferon-alpha produces sustained cytogenetic responses in chronic myelogenous leukemia. Ann Intern Med. 1991;114:532. - PubMed
    1. Kantarjian HM, Smith TL, O’Brien S. Prolonged survival in chronic myelogenous leukemia after cytogenetic response to interferon-α therapy. Ann Intern Med. 1995;122:254–61. - PubMed
    1. Glue P, Fang JW, Rouzier-Panis R, Raffanel C, Sabo R, Gupta SK, Salfi M, Jacobs S and the Hepatitis C Study Group. PEG-interferon alfa-2b: pharmacokinetics, pharmacodynamics, safety and preliminary efficacy data. Clin Pharmacol Ther. 2000;68:556–67. - PubMed

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