Capstone Outline III: Evaluation of mixed energy partial arcs in volumetric modulated arc
therapy for anal cancers with lymph node involvement
Mikayla Eskens, Helen Nguyen, and Will Deere
University of Wisconsin – La Crosse
I. Abstract
A. This will be left blank until the end of the semester.
II. Introduction
A. While creating a radiation therapy treatment plan, medical dosimetrists are able to
utilize photons of varying energies depending on the depth of the planning target
volume (PTV).
1. Deep-seeded tumors require higher energy photons because of their ability
to penetrate through matter. Tumors that are more superficial require low
energy photons. This is also the case when skin irradiation is desirable.
2. Considering the typical patient habitus observed in many clinics today,
additional focus is placed on the dosimetric benefits in using higher
treatment energies.
3. A study comparing photon energies in prostate volumetric modulated arc
therapy (VMAT) treatments demonstrated lower relative integral dose,
monitor units, skin depth of maximum dose (D max), and bladder volume
receiving 30 Gy (V30) for the 10 MV plans versus the 6 MV plans.1
4. Though higher energies can be beneficial in reaching deep seated tumors,
photon energies higher than 10 MV are not recommended for VMAT
treatments due to the additional dose contributed from photoneutron
contamination.2
5. Additionally, 6 MV and 10 MV VMAT treatments were found to be more
beneficial than using 15 MV photons in a study by Yadav et al.3
6. Some cancers such as those found in the pelvis region range drastically in
depth from the skin surface; these can be difficult to treat and may
necessitate the use of multiple photon energies.
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3. All other structures apart from the target volumes were contoured by a
medical dosimetrist.
B. Normal structures were contoured by a single medical dosimetrist responsible for
carrying out the planning in this study.
1. The structures included the skin, bladder, bowel bag, external genitalia or
vagina, left femur, and right femur.
2. In cases where the patient’s CT included contrast in the bowel, the
contrast was also contoured to allow for Hounsfield Unit (HU)
corrections.
3. A Truebeam Couch structure was also added to all CT images for
consistency during the planning process.
Treatment Planning
A. All patients in this study were prescribed a prescription treatment of 1.8 Gy over
25 fractions for a total of 45 Gy delivered.
1. This prescription was used for a curative intent, instead of palliative.
2. All parameters used for creating the treatment plans in this study remained
consistent between patients.
B. Three treatment plans were created for each patient on the Eclipse treatment
planning system by Varian.
1. These plans included one plan using 6 MV photons, one using 10 MV
photons, and one plan that used both 6 MV and 10 MV photons.
i. A 6 MV plan was created with a prescription of 1.8 Gy over 10
fractions, also a 10 MV plan was created with a prescription of 1.8
Gy over 15 fractions.
ii. These two plans were then summed in order to create the mixed
energy VMAT plan that delivered a total of 45 Gy over 25
fractions.
2. Each treatment plan used a VMAT technique with 2 arcs, each of which
covered 359°.
i. The collimator angle for the first arc was set to 10° and the
collimator angle for the second arc was set to 350°.
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ii. Collimator jaws were set to encompass the PTV structure with a
margin of 0.5-2 cm depending on the specific jaw.
C. Optimization structures were contoured by the medical dosimetrist responsible for
carrying out the planning in this study.
1. Optimization structures included were the Opti Bowel Bag and Opti
Bladder structures.
1. The Opti Bowel Bag structure was created by cropping the bowel bag
normal structure from going into the PTV, with a 0.1 cm margin.
2. Similarly, the Opti Bladder structure was created by cropping the bladder
normal structure from going into the PTV, with a 0.1 cm margin.
D. All treatment plans were optimized to the set prescription dose and referenced set
OAR constraints.
1. All plans were normalized to the PTV target volume so that 95% of the
PTV received 100% of the prescription dose.
2. Single energy plans were optimized to the full prescription dose, while the
two plans used to create the mixed energy plan sum were optimized to
their respective partial prescription doses.
3. Plans were optimized a second time to meet OAR constraints as proposed
by Quantitative Analyses of Normal Tissue Effects in the Clinic
(QUANTEC) and the Radiation Therapy Oncology Group (RTOG). 13
Plan Comparisons
A. The three treatment plan types created for each patient were compared.
1. The three plan types included the 6 MV photon plan with full prescription
dose, the 10 MV photon plan with full prescription dose, and the mixed
energy plan sum created from the 6 MV and 10 MV plans with partial
prescription doses.
2. The comparisons were in terms of OAR sparing, monitor unit (MU) usage,
and PTV coverage
B. The OAR considered in comparing the 6 MV and 10 MV single energy plans with
the mixed energy plans were chosen based on QUANTEC and RTOG standards.
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1. The OAR included the bladder, bowel bag, external genitalia or vagina,
and femoral heads.
2. Specific comparison points were included from QUANTEC and RTOG
normal tissue tolerances.
C. The MUs were compared between plan types.
1. The total MUs for each arc of each plan type were totaled and averaged
between patients.
D. The PTV was also compared between plan types in terms of uniformity and
coverage.
1. The PTV coverage was determined using the conformity index.
2. The PTV uniformity was determined using the heterogeneity index.
IV. Results
A. This section should reflect on each patient and the results of the treatment
planning (ex: what the dose to the target was, dose to each OR structure ect.). This
is the section where you pull in your statistical analysis parameters
V. Discussion
A. This is the section that draws your independent research together with your
literature review to discuss your results and if they make sense. Questions you
should answer while writing your discussion: What do you conclude based on the
results of your study? Is this consistent with the literature you found? If not, why
do think that is?
VI. Conclusion
A. Should be a short summary of your paper and answer these questions: Are there
limitations to your study such as sample size, varying clinical sites ect.? What
further research should be done on your topic? You should include citations to
support you research findings
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References
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