Transcript Slide 1

Poster #71
Population Pharmacokinetic Models and
Individualized Bayesian Dose Optimization in HIV-Infected Patients
Michael Neely MD and Roger Jelliffe MD
Los Angeles, California, USA
Laboratory of Applied Pharmacokinetics
www.lapk.org
Introduction
Methods
Results/Case Histories
Standard antiretroviral dosing is size-based for children
and fixed for adults. This may be problematic for an
individual patient.
Antiretroviral population pharmacokinetic models, each with oral
absorption into a single compartment, were constructed using the
MM-USC*PACK
software
collection
[14]
(available
at
www.lapk.org).
Patient 1 was a 13-year old antiretroviral-naïve African boy (Tanner stage 2), started on an
efavirenz-based regimen at the recommended dose for his age. After 2 weeks, his mother
reported that he was too drowsy to attend school, more severe than the typical transient
drowsiness after starting efavirenz. Suspecting that he was a genetic slow metabolizer, we
empirically reduced his dose by half, and a week later measured a serum concentration of 1.37
mg/L 22 hours after his previous dose. His 24-h trough concentration was predicted to remain
above a target of 1 mg/L [22]; therefore, he continued on this dose. A follow-up sample
confirmed his therapeutic concentrations on 50% dose, and he has maintained an undetectable
HIV viral load with no further somnolence for the past 2 years. (Figure 1A)
If the patient is not “average” then the “average” dose may not achieve
the efficacy goal, or may be toxic.
Dose-dependent and dose-independent toxicity are difficult to
distinguish.
Sub-optimal adherence may be undetected prior to development of
virologic failure and resistance; alternatively, sub-optimal dosing may
be mistaken for poor adherence.
There is little or no information on when to change from pediatric to
adult dosing.
There is no ability to adjust the recommended dose in an individual
patient with any assurance of success.
PK parameter estimates obtained or derived from over 30 published
studies were used to generate, by Monte Carlo simulation with noise,
populations of n=50 for each drug. Final parameter values for the
models in this report are shown in Table 1.
Simulated populations were then analyzed using the Non-Parametric
Adaptive Grid (NPAG) program in MM-USC*PACK [15] to generate a
population PK model for each antiretroviral drug.
The models were applied as part of comprehensive clinical care to
outpatients in our HIV clinic using MM-USC*PACK’s multiple-model,
Bayesian adaptive control to individualize therapy.
All of these problems can cause poor outcomes: viral
resistance, toxicity, unnecessary regimen changes or
combinations of these.
Drug
Population
ka
Vd
CL
Nelfinavir [16]
Children
0.4 h-1
6.4 L/kg
1.0 L/h·kg
There are now several clinical investigations [1-7] and numerous
reviews or position papers, e.g. [8-13], that affirm the usefulness of
incorporating measurement of antiretroviral drug concentrations into
the clinical management of selected HIV-infected patients.
Efavirenz [17,18]
Children
0.3 h-1
4.2 L/kg
0.1 L/h·kg
fos-Amprenavir [19,20] Adults
3.0 h-1
5.7 L/kg
0.7 L/h·kg
Atazanavir [21]
1.0 h-1
86.2 L
8.1 L/h
Here, we report four case vignettes of HIV-infected patients
whose therapy was optimized using an approach and
software developed in our lab. These vignettes illustrate the
benefit of dose individualization and optimization in
common clinical scenarios.
References
[1] Fletcher CV, Anderson PL, Kakuda TN et al. Concentration-controlled compared with conventional antiretroviral therapy for HIV infection.
AIDS. 2002; 16(4):551-560.
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indinavir-associated renal toxicity. J Antimicrob Chemother 2006 Jun. 1957;1161-1167.
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Antimicrob Chemother 2007 Oct. 1960;897-900.
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[7] Wasmuth JC, Lambertz I, Voigt E et al. Maintenance of indinavir by dose adjustment in HIV-1-infected patients with indinavir-related
toxicity. Eur J Clin Pharmacol 2007 Oct. 1963;901-908.
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18(12):825-834.
Adults
Table 1: Mean model parameter values. Models based on pediatric
studies were used for patients with a Tanner Sexual Maturity Rating
stage ≤3.
[13] Acosta EP, King JR. Methods for integration of pharmacokinetic and phenotypic information in the treatment of infection with human
immunodeficiency virus. Clin Infect Dis. 2003; 36(3):373-377.
[14] Jelliffe RW. The USC*PACK PC programs for population pharmacokinetic modeling, modeling of large kinetic/dynamic systems, and
adaptive control of drug dosage regimens. Proc Annu Symp Comput Appl Med Care. 1991;922-924.
[15] Bustad A, Terziivanov D, Leary R et al. Parametric and nonparametric population methods: their comparative performance in analysing a
clinical dataset and two Monte Carlo simulation studies. Clin Pharmacokinet. 2006; 45(4):365-383.
[16] Hirt D, Urien S, Jullien V et al. Age-related effects on nelfinavir and M8 pharmacokinetics: a population study with 182 children.
Antimicrob Agents Chemother. 2006; 50(3):910-916.
[17] Csajka C, Marzolini C, Fattinger K et al. Population pharmacokinetics and effects of efavirenz in patients with human immunodeficiency
virus infection. Clin Pharmacol Ther. 2003; 73(1):20-30.
[18] Starr SE, Fletcher CV, Spector SA et al. Efavirenz liquid formulation in human immunodeficiency virus-infected children. Pediatr Infect
Dis J. 2002; 21(7):659-663.
[19] Wire MB, Shelton MJ, Studenberg S. Fosamprenavir : clinical pharmacokinetics and drug interactions of the amprenavir prodrug. Clin
Pharmacokinet. 2006; 45(2):137-168.
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lopinavir exposure: ACTG protocol A5143 results. AIDS. 2005; 19(2):145-152.
[21] Colombo S, Buclin T, Cavassini M et al. Population Pharmacokinetics of Atazanavir in Patients with Human Immunodeficiency Virus
Infection. Antimicrob Agents Chemother. 2006; 50(11):3801-3808.
[22] Kappelhoff BS, Crommentuyn KM, de Maat MM et al. Practical guidelines to interpret plasma concentrations of antiretroviral drugs. Clin
Pharmacokinet. 2004; 43(13):845-853.
[23] Gonzalez de Requena, D. et al. Atazanavir Ctrough is associated with efficacy and safety: definition of therapeutic range. Poster Abstracts,
12th Conference on Retroviruses and Opportunistic Infections in Boston, MA. Abstract #645, 2005
Patient 2 was a 10 year-old girl (Tanner stage 2) who weighed 30.7 kg. Based on the standard
pediatric dose of 55 mg/kg, given formulation limitations, she was prescribed 1875 mg. Since
the recommended “maximum” is the adult dose of 1250 mg, we measured a random serum
concentration of 4.9 mg/L 4 hours after her previous dose to ensure that she was not in a toxic
range. Her predicted peak concentration was 5.5 mg/L and her 12-h trough was 2.1 mg/L, both
within a suggested therapeutic range of 1 - 6 mg/L [22], and she never demonstrated toxicity
despite the continued “supra-maximal” dose. (Figure 1B)
Patient 3 was a 45 year-old woman (Tanner stage 5) with a long history of medication
intolerance. She was started on a fos-amprenavir containing regimen (without ritonavir), 2 x
700 mg tablets twice daily. After starting the new regimen, she complained of daytime fatigue,
which she attributed to the morning dose. She enquired about taking the entire dose at night.
Prior to making changes, we measured a serum amprenavir concentration of 1.4 mg/L 4.5
hours after her previous dose. Modeling suggested that although 2800 mg once daily would not
maintain her trough concentration above the minimum target of 0.23 mg/L [22], a regimen of 1
tablet at 8am followed by 3 tablets at 6pm (a 10-14 hour schedule) would achieve this goal. She
was changed to the latter regimen, and has achieved an undetectable viral load without any
further complaints of fatigue. A follow-up level of 0.9 mg/L 4 hours after the morning dose on
the new regimen confirmed that her predicted troughs were likely to be therapeutic. (Figure
1C)
Patient 4 was a 14-year old male (Tanner stage 4) with poor adherence and limited treatment
options. To encourage better adherence, he was changed to a once-daily regimen that included
atazanavir given in combination with low-dose ritonavir. There were no published pediatric PK
data at the time. The usual adult dose of atazanavir is 300 mg when given with ritonavir, so he
was started on 200 mg based on his small size. We obtained a random atazanavir
concentration of 0.782 mg/L 18 hours after his previous dose. His predicted trough
concentration was 0.380 mg/L, above the minimum target of 0.150 mg/L [23], so the dose was
continued. He initially achieved an undetectable viral load but persistently poor adherence
(self-reported) allowed his viral load to rebound partially to about 2000 copies/mL, despite a
second confirmed therapeutic concentration of atazanavir. (Figure 1D)
A
B
C
D
Figure 1 – MM-USC*PACK output for each patient. Black lines are weighted
average Bayesian-posterior predicted concentrations, red dots are measured
serum concentrations, and blue lines are dose events. Intervals between
measured serum concentrations have been compressed for clarity. Target
concentrations have been added as a reference. A) Patient 1, efavirenz; B)
Patient 2, nelfinavir; C) Patient 3; amprenavir given as fos-amprenavir; D)
Patient 4, atazanavir.
Conclusions
Our methods and software for converting reported PK data into population
PK models can be used locally to optimize safety and efficacy in individual
patients.
Successful therapeutic drug management tailored to patients representing
four scenarios was presented:
1) altered metabolism
2) supra- “maximal” doses related to pediatric vs. adult dosing
3) altered dosing schedules
4) dosing with limited relevant published PK data
Individualized Bayesian adaptive control can move population
PK/PD models beyond their current primary domain of drug
development to the optimized care of patients.
Acknowledgements
This work was supported by Department of Health and Human Services, NIH-NIAID, 1 K23 AI076106-01 and NIH-NBIB, R01
EB005803-01A1