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Daunomycin Pharmacokinetics in Children

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... Pharmacokinetics in Children. Stacey Berg, MD. Anthracyclines widely used in pediatric cancer ... Anticancer drug dosing in children based on body size ... – PowerPoint PPT presentation

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Title: Daunomycin Pharmacokinetics in Children


1
Daunomycin Pharmacokinetics in Children
  • Stacey Berg, MD

2
Background
  • Anthracyclines widely used in pediatric cancer
  • Doxorubicin mostly in solid tumors
  • Daunomycin mostly in leukemias

3
Background
  • Anticancer drug dosing in children based on body
    size
  • Concern when patient deviates from ideal body
    weight
  • Adult data decreased doxorubicin clearance,
    increased half-life with increased IBW
  • Scanty data for children

4
Doxorubicin PK in children
  • 3 studies, all single samples
  • Clearance 400 ml/min/m2
  • 15-fold variability
  • No clear correlation with age, BMI, weight
  • Difference in Cmax between WBC gt50,000, WBC
    lt10,000

5
  • Glaser Pediatric Research Foundation study of
    doxorubicin and body composition in children
  • COG study of daunomycin

6
GPRN study objectives
  • Evaluate relationship between obesity and
    doxorubicin PK in children
  • Correlate PK parameters and body mass index, body
    composition
  • Explore PK parameters and patient characteristics
    (age, gender, ethnicity), labs

7
Eligibility
  • 1 - 21 years old
  • Informed consent
  • Doxorubicin over 1 or 2 days, not continuous
    infusion
  • Bilirubin ULN
  • ALT/AST 3x ULN
  • Weight 12 kg
  • Doxorubicin dose based on true body weight

8
Data Collection
  • Height, weight, BSA
  • AST/ALT/bilirubin/TP/alb/Cr/CBC
  • Concomitant medications
  • DEXA scan for body composition
  • PK samples (0 - 48 hr adjusted for 1 or 2 day
    schedule)

9
Patient characteristics
22 completed subjects
  • 16 male, 6 female
  • 10 Hispanic, 10 Caucasian, 2 Asian
  • Median age 15 yr (range 3-21)
  • Median body fat 25 (range 15-36)
  • Median BMI 20 kg/m2 (range 13-30)

10
HPLC Assay Development
  • Solid phase extraction
  • Reverse-phase HPLC with fluorescence detection
  • Inter-, intra-day CV in plasma lt 7
  • LLQ 2 ng/ml (4 nM)

11
Sample chromatogram in plasma
Dauno (IS)
Dox
Doxol
12
5 compartment model
doxorubicin
doxorubicinol
3
5
infusion
k31
k13
k54
k45
k12
k14
V1
V4
2
k21
k40
k10
13
Modeled PK 1 infusions
14
Modeled PK 2 infusions
15
PK Parameters
From ADAPT model
  • Dox median clearance 390 ml/m2/min (range
    35-1280)
  • Dox terminal t1/2 28 hr (11-70 )
  • Doxol terminal t1/2 39 hr (2-91 )
  • Doxol clearance 37 ml/min/m2 ( 0-284)
  • Similar to published adult data

16
Dox clearance v. BMI
17
Dox clearance v. body fat
18
BMI is related to body fat
19
Dox half-life v. body fat
20
Dox clearance v. age
21
Non-significant correlations
BMI, zBMI, or body fat with
  • Dox volume of distribution
  • Doxol clearance
  • Doxol volume of distribution
  • Doxol half-life

22
Where we are
  • Doxorubicin clearance decreases with increasing
    BMI
  • Doxorubicin clearance tends to decrease with
    increasing body fat
  • Most analysis still ongoing
  • Correlations with labs
  • Multivariate analysis
  • Population model

23
COG daunomycin study
Similar and expanded
  • Describe dauno PK in children
  • Explore BMI/body composition effects on PK
  • Explore correlations with age, gender,
    race/ethnicity
  • Explore relationship between PK and AEs
  • Explore relationship between PK and organ
    function labs

24
COG daunomycin study
  • Groupwide
  • Two year accrual
  • Built-in reminder of study in registration system

25
COG Study
  • Age 21 yr
  • Any diagnosis
  • No specific organ function
  • Any 1 or 2 day dauno infusion lt 24 hrs
  • Coordinate with leukemia study

26
ALL study
  • Impact of obesity on PK in HR-ALL
  • Explore PK vs. SER/RER, EFS, OS
  • Prednisone, vincristine, daunomycin, asparaginase
    in induction
  • Narrower eligibility (age 10 yr, registration
    on AALLL0232)
  • Shared daunomycin PK

27
Study plan
  • Height, weight
  • CBC, LFTs, Cr
  • DXA for body composition at participating
    institutions
  • Intensive PK sampling
  • Collect concomitant meds
  • Collect AEs for cycle with PK

28
Sample size 100 subjects
  • Detects minimum correlation of 0.32 with a 0.05
    and 90 power
  • High probablility of detecting small increment in
    R2 associated With addition of new variable to
    regression model in mutlivariate analysis
  • Track age- make sure accrue enough younger
    children

29
Challenges
  • Accrual
  • Younger children
  • Technical
  • Drawing through central line
  • Getting daunomycinol

30
Future directions
  • Population modeling
  • Limited sampling for future studies
  • Prospective studies of dose adjustments
  • - Effect of dosing based on IBW
  • - Effect of capping doses for BSA
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