Download presentation

Presentation is loading. Please wait.

Published byMelanie Pafford Modified over 2 years ago

1
A Biologically-Based Model for Low- Dose Extrapolation of Cancer Risk from Ionizing Radiation Doug Crawford-Brown School of Public Health Director, Carolina Environmental Program

2
What’s our task? Extrapolate downwards in dose and dose-rate

3
Having trouble finding the right functional form? No problem. We have in vitro studies to show us that.

4
Cells also die from radiation, so we need to account for that

5
Just use these to create a phenomenological model P TSC (D) = αD + βD 2 S(D) = e -kD P T (D) = (αD + βD 2 ) x e -kD

6
So what’s the big deal? Just fit it! in vitro K d “Fitted” K d

7
Why does it not work?? Model mis-formulation even at lower level of biological organization New processes appear at the new level of biological organization (emergent properties) Processes disappear at the new level of biological organization Incorrect equations governing processes Parameter values differ at the new level of biological organization

8
Why does it not work (continued)?? Dose distributions different at the new level of biological organization Computational problems somewhere Anatomy, physiology and/or morphometry differ at the new level of biological organization Errors in the data provided (exposures, transformation frequency, probability of cancer, etc)

9
Then let’s get a generic modeling framework Exposure conditions Environmental conditions Deposition and clearance Dose distribution Dose- response Probability of effect

10
The environmental, exposure and dosimetry conditions In vitro doses are uniform as given by the authors, and at the dose-rates provided Rat exposures are from Battelle and Monchaux et al studies, under the conditions indicated by the authors Human exposures are from the uranium miner studies in Canada Rat and human dosimetry models using Weibel bifurcating morphology Uses mean bronchial dose in TB region, or dose distributions throughout the TB region and depth in the epithelium

11
The multi-stage nature of cancer Initiation Promotion Progression Cell Death

12
The state vector model

13
3 The Mathematical Development of the SVM Let N i (t) be the number of cell in State i at any time t: Vector represents the state of the Vector represents the state of the cellular community where cellular community where The total cells in all states is denoted: The total cells in all states is denoted: Transformation frequency is calculated by: Transformation frequency is calculated by: Six Differential equations describe the movement of cells through states Six Differential equations describe the movement of cells through states Example: Example:

14
And now for some parameter values: chromosomal aberrations

15
Rate constants for repair rates and transformation rate constants.

16
Inactivation rate constants

17
Then for promotion: removal of contact inhibition I D D D D D D Showing: Complete removal of cell-cell contact inhibition

18
So, does this work for x-rays? The in-vitro data on transformation Pooled data from many experiments for the transformation rate for single ( ) and split (O) doses of X-rays (Miller et al. 1979)

19
Model fit to in vitro data

20
Sensitivity to P ci value

21
Low dose behavior (no adaptive response)

22
Low dose behavior (with adaptive response)

23
But does it work for in vivo exposures to high LET radiation with very inhomogeneous patterns of irradiation? Helpful scientific picture from EPA web site

24
The rat data (Battelle in circles and Monchaux et al in triangles)

25
So, does this work for rats?? Well, not so much……..

26
With dose variability P C (D) = ∫ PDF(D) * (αD + βD 2 ) * e -kD dD

27
Incorporating dose variability GSD = 1, 5, 10 Empirically: lognormal with GSD = 8

28
Deterministic or stochastic?

30
Back to the issue of differentiation, R d/s in the kinetics model

31
Changes in R d/s 1, 2, 4

32
Fits to mining data With depth-dose information Without depth-dose information

33
Inverting the dose-rate effect

34
Conclusions (continued) Good fit to the in vitro data, even at low doses if adaptive response is included (IF you believe the low-dose data!) Reasonable fit to rat and human data at low to moderate doses, but only with dose variability folded in Best fit with R d/s included to account for differentiation pattern in vivo

35
Conclusions Under-predicts human epidemiological data at higher levels of exposure Under-predicts rat data at higher levels of exposure, especially for Battelle data (not as bad for the Monchaux et al data)

36
Why did it not work?? Model mis-formulation even at lower level of biological organization: compensating errors that only became evident at higher levels of biological organization New processes appear at the new level of biological organization: clusters of transformed cells needed to escape removal by the immune system Processes disappear at the new level of biological organization: cell lines too close to immortalization to be valid at higher levels Incorrect equations governing processes: dose- response model assumes independence of steps Parameter values differ at the new level of biological organization: not true for cell-killing, but may be true for repair processes

37
Why does it not work (continued)?? Dose distributions different at the new level of biological organization: we account for the distributions, but we don’t know the locations of stem cells Computational problems somewhere: what exactly are you suggesting here (but perhaps a problem of numerical solutions under stiff conditions)??? Anatomy, physiology and/or morphometry differ at the new level of biological organization: we think we are accounting for this Errors in the data provided: well, not all mistakes are introduced by theoreticians

Similar presentations

OK

OBJECTIVE Quantitate interspecies toxicodynamic differences during neocortical development of the rat and primate brain. BACKGROUND Ethanol is a particularly.

OBJECTIVE Quantitate interspecies toxicodynamic differences during neocortical development of the rat and primate brain. BACKGROUND Ethanol is a particularly.

© 2017 SlidePlayer.com Inc.

All rights reserved.

Ads by Google

Ppt on petroleum industry in india download Download ppt on civil disobedience movement in the 1960s Ppt on hotel management system Ppt on servant leadership Free ppt on food security in india Ppt on 3d tv without glasses Ppt on infosys company profile Ppt on road accidents in india Historical backgrounds for ppt on social media Ppt on limits and derivatives help