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GROUP_4 PRESENTATION

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Title: GROUP_4 PRESENTATION


1
GROUP_4PRESENTATION
  • A NEW LINEAR PROGRAMMING APPROACH TO RADIATION
    THERAPY TREATMENT PLANNING PROBLEMS

2
INTRODUCTION
  • 1.3 million U.S. citizens are newly diagnosed
    with cancer (American Cancer Society 2004)
  • 300,000 patients per year

3
  • Radiation Therapy
  • Can reduce the quality of life
  • Too little radiation dose to the targets
  • Patients life must be balanced
  • To design optimal radiation therapy treatment
    plans

4
Beams of radiation
Clinical targets
Critical structures
5
  • Why is not a single beam usen at radiation??
  • Kill the targets
  • Risk to damage normal cells in critical
    structures located along the along path of the
    beam

6
  • Deliver beams
  • Intersections are the targets
  • Intersection gt The highest radiation dose
  • Low radiation dose gt The critical structures

7
Types of Radiation Therapy
  • Conformal radiation therapy
  • Conventional conformal radiation therapy
  • External beam radiation delivery technique gt
    intensity-modulated radiation therapy
    ( IMRT )

8
IMRT
  • Complex nonuniform dose distributions
  • High radiation doses to targets
  • Limiting the radiation dose for healty cells
  • These dose distributions are obtained by
    dynamically blocking different parts of the beam
  • Optimization techniques

9
FMO Type of Optimization Problems
  • Fluence Map Optimization (FMO) Problems
  • Design an optimal radiation density profile in
    the patient
  • Deliver prescription dose to cancerous cells
  • Not exceed tolerance dose to normal cells

10
OR Approaches To The IMRT Radiation Therapy
  • Quadratic Programming
  • Not allows sufficient flexibility for
    high-quality treatment
  • Global and Mix-integer Pragramming
  • Allows flexibility but
  • not feasible to employ in real-life while
    ensuring the global optimal solution

11
Expected Programming Model
  • Expected Prog. Model should ensure
  • Add flexibility as compared with quadratic
    programming models
  • Prevent difficulties such as multiple local
    optima that occur in mixed-integer and/or
    non-convex global optimization models

12
Goal Of The Paper
  • New approach to the FMO problem
  • Based on employing linear programming
    approximations to convex programming formulations
  • Model ables to incorporate several measures
    (additional aspects) while retaining linearity
  • Duality theory

13
Terminology and Notation
  • Targets are cancerous cells (s1,....,T)
  • Critical Structures are normal cells
    (sT1,....,S)
  • Both cells are called generally as structures
  • (s1,....,S)
  • Each beam is decomposed into small beamlets
    (i1,......,N)
  • Each structure is decomposed into several number
    of voxels (j1,.....,Vs)

14
Notation
Decision Variables
The weight (intensity) of beamlet i ,
i1,.....,N
Parameters
The dose received by voxel j in structure s
from beamlet i at unit intensity
(weight) j1,.....,Vs s1,....,S i1,.....,N
15
Notation
  • Beamlet intensity ?

Dose received by voxels
Linear relationship
Represent dose received by each voxel as a
function of the beamlet intensities as follows
16
Model Formulation of The Paper
  • Basic Constraints are called full-volume
    constraints
  • F1? Deliver minimum prescription dose L to all
    voxels in the targets
  • F2? Do not deliver more than a maximum tolerance
    dose U to all voxels in both targets and
    critical structures

17
Full-Volume Constraints
Lower Bound on the dose received by all voxels
in structure s
Upper Bound on the dose received by all voxels
in structure s
18
Penalty Function and Objective Function
  • Define for each structure, a penalty function of
    the dose received by the voxels in that structure
  • Denote the penalty function for structure s by

19
The Objective Function to Minimize
Scaling term ?
Ensuring penalty functions are insensitive to the
relative sizes in different problems
Is described as a function of z
20
Variable Transformation
  • This transformation simplifies the model
    formulation

21
Model Formulation of the Paper
22
Model Formulation of the Paper
Objective Function
Transformation
Lower Bound (F1)
Upper Bound (F2)
23
Penalty Function
Only voxels that are overdosed are penalized
Underdose penalty function
Overdose penalty function
0 for critical structures
0 for critical structures
Lower doses are always preferred to higher doses
in critical structures
For targets, the overdose and underdose
thresholds will often be chosen to be equal
24
Approximate penalty functions by piecewise-linear
functions
  • By this approximation,
  • They can reformulate their FMO model in a linear
    form as linear programming problem

Penalty functions for a target and a critical
structure
25
Approximation of penalty function by
piecewise-linear convex functions
Each of these variables has zero lower bound and
an upper bound given by the size of the segment
The dose to a voxelgtsum of all segment variables
for that voxel
Decision variablegt
kth linear segment in the piecewise linear
convex penalty function for each voxel (j,s).
26
Our Model Formulation
27
Our Model Formulation
Our model is perfectly linear with several
assumptions
Closed form
We remove both the convexity and the maximum
function
28
Required Values
Following table represents
Values, we use approximate values according to
the paper
29
Required values
is equal to 85 for all voxels in the targets ,
s1,2 (only for targets)
is equal to 100 for all voxels in both targets
and critical structures
is equal to 100 for all targets
is equal to 0 for critical structures and 100 for
targets
30
Required values
is equal to 50 for all voxels in the targets ,
s1,2 (only for targets) and 0 for critical
structures
is equal to 60 for all voxels in the targets ,
s1,2 and 70 for critical structures, s1,2
LETS SOLVE THE MODEL
31
Dose-Volume Histogram (DVH)
  • The fraction of the structures volume ?
  • receives at least a certain amount of dose
  • The value of DVH at dose d ? the fraction of
    voxels in the structure who receives a dose of at
    least d units

32
Partial Volume Constraints
  • Traditional Partial-Volume Constraints
  • Incorporate constraints on the shape and location
    of the DVH of a structure
  • New Class of Partial-Volume Constraints
  • Formulate risk management constraints in terms of
    tail averages

33
New Class of Partial-Volume Constraints
Constrain the average dose in a tail of a given
size as opposed to the max and min dose in that
tail
Linear and has computational advantage
34
Results of The Paper
  • Validate the model,
  • Tuned the parameters of the model by manual
    adjustment,
  • Test robustness

35
  • THANK YOU FOR YOUR LISTENING...
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