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Analysis of Interfractional Setup Errors and Intrafractional Organ Motions during IMRT for Head and

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Title: Analysis of Interfractional Setup Errors and Intrafractional Organ Motions during IMRT for Head and


1
Analysis of Interfractional Set-up Errors and
Intrafractional Organ Motions during IMRT for
Head and Neck Cancers to Define an Appropriate
PTV-margins
Minoru Suzuki, a, b Yasumasa Nishimura, a
Kiyoshi Nakamatsu, a Masahiko Okumura, c
Hisayuki Hashiba, c Ryuta Koike, a Shuichi
Kanamori, a Toru Shibata, a a Department of
Radiation Oncology, Kinki University School of
Medicine, b Radiation Oncology Research
Laboratory, Research Reactor Institute, Kyoto
University c Depatment of Central Radiological
Service, Kinki University School of Medicine
Figs. 4 and 5. The distribution of the
interfractional set-up errors and intrafractional
organ motions of the mandible.
  • The systematic intrafractional organ motion error
    for a specific patient, Sp-intra, is calculated
    as the mean value for intrafractional organ
    motion errors of that patient. The mean of
    Sp-intra over all patients in a given population
    is denoted by µ-intra, whereas its SD is given by
    S-intra. The random intrafractional organ motion
    errors for a specific patient, sp-intra, was
    calculated as the SD of the intrafractional organ
    motion errors from interval to interval. To
    characterize the random errors in a population,
    an appropriate average is calculated over the
    patient group, which is denoted by s-intra .
    Distribution of intrafractional organ motion
    errors in a given population is characterized by
    the set (µ-intra,S-intra, s-intra) as the
    interfractional set-up errors.
  • Deviations of the coordinates of each bony
    landmark in the beam films from those in the
    simulation films were measured as the set-up
    error for each bony landmark.

? The purposes of the present study were to
analyze the interfractional set-up errors and
intrafractional organ motions and to define
appropriate planning target volume (PTV)-
margins.
L-R
Fig. 4 (a)
Fig.4(c)
A-P
Fig. 4 (b)
C-C
9
10
9
m -0.2 S-INTER
1.3 s-INTER 1.0
m -0.1 S-INTER
0.8 s-INTER 0.9
  • To calculate displacement or standard deviations
    (SDs) for systematic and random errors, we
    referred to Rameijer et al. The systematic
    interfractional setup error for a specific
    patient, Sp-INTER, is calculated as the mean
    value for setup errors of that patient. The mean
    of Sp-INTER over all patients in a given
    population is denoted by µ-INTER, whereas its SD
    is given by S-INTER. The random setup error for a
    specific patient, sp-INTER, was calculated as the
    SD of the setup errors from fraction to fraction.
    To characterize the random errors in a
    population, an appropriate average is calculated
    over the patient group, which is denoted by
    s-INTER. Distribution of the interfractional
    setup errors in a given population is
    characterized by the set (µ-INTER, S-INTER,
    s-INTER).

m -0.2 S-INTER
1.0 s-INTER 0.7
9
8
8
8
7
7
7
6
6
Number
6
5
5
5
4
4
4
3
3
3
2
2
2
1
1
1
0
0
0
Materials and Methods
0.6 0.8
0.6 0.8
-0.2 0.0
0.0 0.2
0.2 0.4
0.4 0.6
0.8 1.0
1.0 1.2
1.2 1.4
1.4 1.6
1.6 1.8
1.8 2.0
2.0 2.2
2.2 2.4
2.4 2.6
2.6 2.8
2.8 3.0
3.0 3.2
3.2 3.4
3.4 3.6
3.6 3.8
3.8 4.0
4.0 4.2
4.2 4.4
-0.2 0.0
0.0 0.2
0.2 0.4
0.4 0.6
0.8 1.0
1.0 1.2
1.2 1.4
1.4 1.6
1.6 1.8
1.8 2.0
2.0 2.2
2.2 2.4
2.4 2.6
2.6 2.8
2.8 3.0
3.0 3.2
0.0 0.2
0.2 0.4
0.4 0.6
0.6 0.8
0.8 1.0
1.0 1.2
1.2 1.4
1.4 1.6
1.6 1.8
1.8 2.0
2.0 2.2
2.2 2.4
2.4 2.6
2.6 2.8
2.8 3.0
3.0 3.2
-2.6 -2.4
-2.4 -2.2
-2.2 -2.0
-2.0 -1.8
-1.8 -1.6
-1.6 -1.4
-1.4 -1.2
-1.2 -1.0
-1.0 -0.8
-0.8 -0.6
-0.6 -0.4
-0.4 -0.2
-3.2 -3.0
-3.0 -2.8
-2.8 -2.6
-2.6 -2.4
-2.4 -2.2
-2.2 -2.0
-2.0 -1.8
-1.8 -1.6
-1.6 -1.4
-1.4 -1.2
-1.2 -1.0
-1.0 -0.8
-0.8 -0.6
-0.6 -0.4
-0.4 -0.2
-0.2 0.0
-2.6 -2.4
-2.4 -2.2
-2.2 -2.0
-2.0 -1.8
-1.8 -1.6
-1.6 -1.4
-1.4 -1.2
-1.2 -1.0
-1.0 -0.8
-0.8 -0.6
-0.6 -0.4
-0.4 -0.2
Fig. 5 (a)
Fig. 5 (b)
Fig. 5 (c)
L-R
A-P
Interfractional set-up error analysis
12
12
10
10
  • Consecutive ten patients with head and neck
    cancers treated with IMRT were evaluated for
    analysis of the interfractional set-up errors.
    Table 1 shows the summary of patients
    characteristics.

8
8
Number
6
6
Interfractional setup errors and intrafractional
organ motion errors
4
4
2
  • The values for the set of parameters (µ-INTER,
    S-INTER, s-INTER) and (µ-intra, S-intra, s-intra)
    measured for four bony landmarks are shown in
    Tables 3and 4, respectively.

2
  • All patients were immobilized with a
    thermoplastic mask covering the head, neck and
    shoulders (Uni-frame form MED-TEC, Orange City,
    IA, USA.) (Fig.1).

Intrafractional organ motion analysis
0
0
1.2 1.4
0.6 0.8
0.0 0.2
0.2 0.4
0.4 0.6
0.8 1.0
1.0 1.2
-0.2 0.0
0.6 0.8
0.0 0.2
0.2 0.4
0.4 0.6
0.8 1.0
1.0 1.2
1.2 1.4
1.4 1.6
1.6 1.8
1.8 2.0
-1.0 -0.8
-0.8 -0.6
-0.6 -0.4
-0.4 -0.2
-0.2 0.0
-3.8 -3.6
-3.6 -3.4
-3.4 -3.2
-3.2 -3.0
-3.0 -2.8
-2.8 -2.6
-2.6 -2.4
-2.4 -2.2
-2.2 -2.0
-2.0 -1.8
-1.8 -1.6
-1.6 -1.4
-1.4 -1.2
-1.2 -1.0
-1.0 -0.8
-0.8 -0.6
-0.6 -0.4
-0.4 -0.2
  • In an analysis of intrafractional organ motion,
    nine with head and neck cancers and three with
    malignant glioma were evaluated. Table 2
    shows the summary of patient characteristics.
  • The method for intrafractional organ motion
    analysis was as follows.
  • First, on the X-ray simulator (Ximatoron EX,
    Varian Assoc., Palo Alto, CA) with same table
    coach as our treatment system (Clinac-600C
    accelerator, Varian Assoc., Palo Alto, CA, USA),
    the patient was positioned and fixed with
    immobilizing device used at irradiation.
  • Second, for 15 minutes, the AP and lateral
    images were digitally stored at 3 minutes
    interval (6 times) (Fig. 3).
  • Third, the coordinates of the same bony landmarks
    were determined using the software in Somavision.
  • In the present study, intrafractional organ
    motion error was defined as deviation of the
    coordinate of each landmark at each interval from
    that at the initial image taken at the start of
    the analysis.

Displacement (mm)
Fig.1
PTV- and PRV-margin
  • Stroom et al. proposed an equation for
    appropriate PTV margin recipe, PTV-margin 2S
    0.7s. McKenzie et al. proposed the recommended
    margin around the ORs, the planning organs at
    risk volume (PRV-margin). They proposed an
    equation of PRV-margin 1.3S 0.5s for serial
    ORs or small, parallel ORs.
  • The calculated PTV-margins were summarized in
    Table 6.
  • ? At our department, as one of the procedures for
    quality assurance (QA) of the IMRT, we took two
    orthogonal, anterior-posterior (AP) and lateral
    films, for verification of the isocenter. The
    orthogonal films taken with treatment beam (beam
    film) were referred to those taken on the table
    of the X-ray simulator (simulation film).
  • Analysis of the interfractional set-up error was
    performed by comparing total 170 beam films (85
    AP and 85 lateral films) with 20 simulation films
    (10 AP and 10 lateral films) for the 10 patients.
    Since the magnitude of the movement of the head
    and neck tumors may be varied according to the
    location of the tumors, the each position of four
    visible bony landmarks relative to the isocenter
    was assessed. The four landmarks included
    maxilla, mandible, skull base, and cervical
    vertebrae (Fig.2).

Fig. 3
  • The distribution of the interfractional setup
    errors of the mandible and the intrafractional
    organ motion errors is shown graphically in Figs
    4 (a) - (c) and Figs 5 (a)-(c).
  • The validity of the 5-mm PTV-margin at our
    institution can be verified because of small
    variations in the interfractional set-up errors
    and intrafractional organ motion errors.
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