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TREATMENT PLANNING II: PATIENT DATA, CORRECTIONS, AND SET-UP

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Basic depth-dose data and isodose curves are usually measured in a cubic water ... Sliding the isodose chart up or down, depending on whether there is tissue ... – PowerPoint PPT presentation

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Title: TREATMENT PLANNING II: PATIENT DATA, CORRECTIONS, AND SET-UP


1
TREATMENT PLANNING II PATIENT DATA, CORRECTIONS,
AND SET-UP
?????????The Physics of Radiation Therapy.
Faiz M. Khan
2
TREATMENT PLANNING II
  • Basic depth-dose data and isodose curves are
    usually measured in a cubic water phantom, beams
    incident normally on the flat surface at
    specified distance
  • The patient's body, however, is neither
    homogeneous nor flat in surface contour.
  • correction for contour curvature, and tissue
    inhomogeneities and patient positioning.

3
ACQUISITION OF PATIENT DATA
  • Accurate patient dosimetry is only possible when
    sufficiently accurate patient data are available
  • body contour, outline, and density of relevant
    internal structures, location, and extent of the
    target volume

4
Body Contours
ACQUISITION OF PATIENT DATA
  • Acquisition of body contours and internal
    structures is best accomplished by imaging
  • CT and MRI .
  • Scans are performed with the patient positioned
    the same way as for actual treatment
  • lead wire
  • measure antero/posterior and/or lateral diameters
    of the contour
  • Optical and ultrasonic

5
Some important points for contour making
ACQUISITION OF PATIENT DATA
  • same position as used in the actual treatment.
  • Horizontal line representing the tabletop
  • Important bony landmarks must be indicated on the
    contour.
  • Checks of body contour during the treatment
    course
  • If body thickness varies significantly , contours
    should be determined in more than one plane.

6
Internal Structures
  • Transverse Tomography
  • Computed Tomography
  • Magnetic Resonance Imaging
  • Ultrasound

7
Internal Structures
Transverse Tomography
  • provide cross-sectional information of internal
    structures in relation to the external contour
  • poor contrast and spatial resolution

8
Internal Structures
Computed Tomography
  • the distribution of attenuation coefficients
    within the layer
  • an image can be reconstructed that represents
    various structures with different attenuation
    properties.

9
Internal Structures
Computed Tomography
  • CT numbers
  • related to attenuation coefficients
  • Hounsfield numbers
  • CT numbers normalized

10
Internal Structures
Computed Tomography
  • CT numbers
  • it is possible to infer electron density
    (electrons cm-3)

11
Internal Structures
Computed Tomography
  • The CT information is useful in two aspects of
    treatment planning
  • delineation of target volume and the surrounding
    structures in relation to the external contour
  • providing quantitative data (in the form of CT
    numbers) for tissue heterogeneity corrections

12
Internal Structures
Magnetic Resonance Imaging
  • MRI has developed, in parallel to CT
  • advantages over CT
  • scan directly in axial, sagittal, coronal, or
    oblique planes
  • not involving the use of ionizing radiation
  • higher contrast
  • Better imaging of soft tissue tumor

13
Internal Structures
Magnetic Resonance Imaging
  • Disadvantages compared with CT
  • inability to image bone or calcifications
  • longer scan acquisition time
  • technical difficulties due to small hole of the
    magnet and
  • magnetic interference with metallic objects

14
Internal Structures
Ultrasound
  • Ultrasound can provide useful information in
    localizing many malignancy-prone structures in
    the lower pelvis, retroperitoneum, upper abdomen,
    breast, and chest wall

15
TREATMENT SIMULATION
TREATMENT SIMULATION
  • uses a diagnostic x-ray tube but duplicates a
    radiation treatment unit in terms of its
    geometrical, mechanical, and optical properties.

16
TREATMENT SIMULATION
TREATMENT SIMULATION
  • By radiographic visualization of
  • internal organs,
  • correct positioning of fields
  • and shielding blocks
  • can be obtained in relation to external landmarks
  • fluoroscopic capability by dynamic visualization

17
TREATMENT SIMULATION
TREATMENT SIMULATION
  • An exciting development in the area of simulation
    is that of converting a CT scanner into a
    simulator
  • CT-SIM

18
TREATMENT VERIFICATION
TREATMENT VERIFICATION
  • Port Films
  • Electronic Portal Imaging (EPI)
  • Cone Beam CT
  • MV-CT ( Tomotherapy )

19
TREATMENT VERIFICATION
Port Films
  • The primary purpose of port filming is to verify
    the treatment volume under actual conditions of
    treatment
  • the image quality with the megavoltage x-ray beam
    is poorer than with the diagnostic or the
    simulator film

20
TREATMENT VERIFICATION
Port Films
21
TREATMENT VERIFICATION
Port Films
  • Limitations of port film
  • Viewing is delayed because of the time required
    for processing
  • Its impractical to do port films before each
    treatment
  • Film image is of poor quality especially for
    photon energies greater than 6MV

22
TREATMENT VERIFICATION
  • Electronic portal imaging device ( EPID )
  • Mount on the linac
  • Real-time, digital feedback to the user.

23
  • Portal imaging devices
  • fluoroscopy-based systems
  • liquid filled ionization chamber matrices
  • amorphous silicon based system

24
  • Fluoroscopy-based systems
  • The detector quantum efficiency ( DQE ) of these
    systems is limited by electronic noise in the
    camera system and poor optical coupling between
    the light emitter and the camera system (only
    0.01 of the emitted photons reach the camera)

25
  • liquid filled ionization chamber matrices
  • The maximum spatial resolution is 2.3 mm x 2.9
    mm, increasing to 2.3 mm x 4.5 mm depending on
    acquisition mode

26
  • amorphous silicon based system
  • less excess dose to be delivered to the patient
    per portal image and yet yielding a superior
    image quality, resolution of 0.784 x 0.784 mm2.

27
CORRECTIONS
CORRECTIONS FOR CONTOUR IRREGULARITIES
  • Effective Source-to-Surface Distance Method
  • Tissue-air (or Tissue-maximum) Ratio Method
  • lsodose Shift Method

28
CORRECTIONS
Effective SSD Method
29
CORRECTIONS
TAR Method
  • ratio depend on only of the depth and the field
    size at that depth

30
CORRECTIONS
lsodose Shift Method
  • Sliding the isodose chart up or down, depending
    on whether there is tissue excess or deficit
    along that line, by an amount kh where k is a
    factor less than 1

31
CORRECTIONS
CORRECTIONS FOR TISSUE INHOMOGENEITIES
  • The presence of inhomogeneities will produce
    changes in the dose distribution, depending on
    the amount and type of material present and on
    the quality of radiation

32
CORRECTIONS
CORRECTIONS FOR TISSUE INHOMOGENEITIES
  • The effects of tissue inhomogeneities
  • changes in the absorption of the primary beam and
    the associated pattern of scattered photons
  • primary beam points that lie beyond the
    inhomogeneity,
  • Scattered points near the inhomogeneity
  • changes in the secondary electron fluence
  • tissues within the inhomogeneity and at the
    boundaries.

33
CORRECTIONS
CORRECTIONS FOR TISSUE INHOMOGENEITIES
  • Corrections for Beam Attenuation and Scattering
  • TAR method, Power law TAR method , Equivalent TAR
    method, Isodose shift method, Typical correction
    factors
  • Absorbed Dose within an Inhomogeneity

34
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • TAR method
  • d' d1 ?1 d2 d3
  • d is the actual depth of P from the surface

35
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • Power Law Tissue-air Ratio Method
  • correction factor does depend on the location of
    the inhomogeneity relative to point P but not
    relative to the surface or in the build-up region

36
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • Power Law Tissue-air Ratio Method
  • A more general form, provided by Sontag and
    Cunningham
  • allows for correction of the dose to points
    within an inhomogeneity as well as below it.

37
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • Equivalent Tissue-air Ratio Method
  • correctly predicted the effect of scattering
    structures depends on their geometric arrangement
    with respect to point P

38
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • Equivalent Tissue-air Ratio Method
  • d' is the water equivalent depth, d is the actual
    depth, r is the beam dimension at depth d,
  • r' r ?' scaled field size dimension

39
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • lsodose Shift Method
  • manually correcting isodose charts for the
    presence of inhomogeneity

40
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • Typical Correction Factors
  • None of the methods discussed above can claim an
    accuracy of 5 for all irradiation conditions
    encountered in radiotherapy
  • Tang et al. have compared a few commonly used
    methods against measured data using a
    heterogeneous phantom containing layers of
    polystyrene and cork

41
CORRECTIONS
Corrections for Beam Attenuation and Scattering
  • Typical Correction Factors
  • Their results (Tang et al. )
  • the TAR method overestimates the dose for all
    energies
  • the ETAR is best suited for the lower-energy
    beams (?6 MV)
  • the generalized Batho method is the best in the
    high-energ range (?10 MV)

42
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone Mineral

43
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone-tissue Interface
  • Soft Tissue in Bone

44
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone-tissue Interface
  • Soft Tissue Surrounding Bone

45
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone-tissue Interface
  • Soft Tissue Surrounding Bone
  • forward scatter
  • For energies up to 10 MV, the dose at the
    interface is initially less than the dose in a
    homogeneous soft tissue medium but then builds up
    to a dose that is slightly greater than that in
    the homogeneous case.
  • For higher energies, there is an enhancement of
    dose at the interface because of the increased
    electron fluence in bone due to pair production

46
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone-tissue Interface
  • Soft Tissue Surrounding Bone

47
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone-tissue Interface
  • parallel-opposed beams

48
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Bone-tissue Interface
  • parallel-opposed beams

49
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Lung Tissue
  • Dose within the lung tissue is primarily governed
    by its density
  • But in the first layers of soft tissue beyond a
    large thickness of lung, there is some loss of
    secondary electrons

50
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Lung Tissue
  • problem of loss of lateral electronic equilibrium
    when a high-energy photon beam traverses the lung
  • dose profile to become less sharp
  • The effect is significant for small field sizes (
    lt 6 x 6 cm ) and higher energies ( gt6 MV )

51
CORRECTIONS
Absorbed Dose within an Inhomogeneity
  • Air Cavity
  • The most important effect of air cavities in
    megavoltage beam dosimetry is the partial loss of
    electronic equilibrium at the cavity surface
  • The most significant decrease in dose occurs at
    the surface beyond the-cavity, for large cavities
    (4 cm deep) and the smallest field (4 x 4 cm)

52
TISSUE COMPENSATION
  • To preserve the skin-sparing properties of the
    megavoltage photon beams, the compensator is
    placed a suitable distance (gt20 cm) away from the
    patient's skin

53
??
  • 1. ??????????????????
  • (1) CT (2) PET (3) MRI (4) Ultrasound
  • 2. ??????????????????????
  • (1) CT (2) Simulator (3) MRI (4)
    ultrasound
  • 3. ??????????????????????????????
  • (1) CT (2) Simulator (3) MRI (4)
    ultrasound
  • 4. ????,?? Hounsfield number ???
  • (1) 0 (2) -1000 (3) 1000 (4) 500
  • 5. ????????????????
  • (1) CT (2) Simulator (3) MRI (4) CT-SIM
  • 6. ??????????? TREATMENT VERIFICATION ?
  • (1) Port Films (2) Electronic Portal
    Imaging (3) Cone Beam CT (4) MRI

54
??
  • 6. ???? TREATMENT VERIFICATION ???????????????
  • (1) Port Films (2) Electronic Portal
    Imaging (3) Cone Beam CT (4) MRI
  • 7. ??????????????????
  • (1) Effective SSD (2) TAR method
  • (3) lsodose Shift Method
  • (4) Power Law Tissue-air Ratio Method

55
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56
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57
PDD - Dependence on Source-Surface Distance
  • PDD increases with SSD
  • the Mayneord F Factor ( without considering
    changes in scattering )
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