Pelvis Lab-1
Pelvis Lab-1
Plan 1
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Plan 1
Plan 1
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Plan 1
Plan 2: Change the PA field to a higher energy and calculate the dose.
Describe how the isodose distribution changed and why?
o I changed the PA field from 6X to 15X. The isodose lines shifted more anteriorly
so that more of the PTV is being covered. I noticed a bigger difference/more of a
shift in the lower isodose lines compared to the 95% or 100% lines. This is
because with a higher energy, the dose is being pushed deeper into the body.
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The dmax for 15MV is 3.0 cm. The hot spot was also reduced from 174.8% to
154.0%.
Using your DVH to confirm, what percent of the PTV is receiving 100% of the
prescription dose?
o 54.35% of the PTV is receiving 100% of the prescription dose.
Plan 2
Plan 2
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Plan 2
Plan 2
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Plan 3: Insert a left lateral field with a 1 cm margin around the PTV. Copy and oppose the left
lateral field to create a right lateral field. Use the lowest beam energy available for all 3 fields.
Calculate the dose and apply equal weighting to all 3 fields.
Describe the isodose distribution. What change did you notice?
o The isodose distribution around the PTV expanded even more anteriorly, giving
the PTV more coverage with the higher dose levels. However, the isodose
distribution has spread out more laterally in the patient, so there’s more dose at
the sides of their body and around the femoral heads.
Where is the hot spot and what is it?
o The hot spot went down to 113.8% and it’s located posteriorly in the patient,
about 6 cm from the skin surface, which is deeper in the body than it was before.
It’s gotten closer to the PTV but is still outside of it.
What do you think creates the hot spot in this location?
o The hot spot is still very posterior in the patient because the beams are only
entering from the posterior and lateral angles and since they’re the lowest
energy, the dose isn’t penetrating as far. To push the hot spot more anteriorly
towards the PTV, I think we’d need to add a beam entering from the AP or we
would have to increase the energy on the existing beams so that more dose is
being deposited at a greater depth.
Plan 3
Plan 3
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Plan 3
Plan 3
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Plan 4: Increase the energy of all 3 fields and calculate the dose.
Describe how this change in energy impacted the isodose distribution.
o The isodose distribution changed so that the higher doses are covering more
anteriorly and medially in the patient. Essentially, the dose got pushed deeper
into the body. More of the PTV is being covered with the higher isodose lines.
The higher doses that were in the lateral parts of the patient near the hips also
got pushed more medially, so it cooled down the sides of the body.
In your own words, summarize the benefits of using a multi-field planning approach?
(Refer to Khan Physics for benefits of multiple fields)
o Using multiple fields is beneficial in distributing the dose more evenly to the
treatment area. The more fields you have, the lower the weighting is for each
field (each field is individually contributing less) and the dose build-up is highest
where the fields meet. In comparison, with just one field, the dose is only being
distributed from one angle. This creates more of a hot spot at the surface of the
skin where the beam is entering and PTV coverage will not be as sufficient.
Compared to your single field in plan 2, what percent of the PTV is now receiving 100%
of the prescription dose? Use a DVH to show how you obtained this response.
o 61.9% of the PTV is receiving 45 Gy, compared to 54.3% of the PTV receiving 45
Gy in plan 2.
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Plan 4
Plan 4
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Plan 4
Plan 4
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Plan 5: Using your 3 high energy fields from plan 4, adjust the field weights until you are
satisfied with the isodose distribution.
Plan 5
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Plan 5
Plan 5
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Plan 6: Insert a wedge on each lateral field. Continue to add thicker wedges on both lateral
fields until you are satisfied with your final isodose distribution. Note: When you replace a
wedge on the left, replace it with the same wedge angle on the right. Also, if you desire to
adjust the field weights after wedge additions, go ahead and do so.
What final wedge angle and orientation did you choose? To define the wedge
orientation, describe it in relation to the patient. (e.g., Heel towards anterior of
patient, heel towards head of patient..)
o 30IN on the left lateral and 30OUT on the right lateral. The heel for both is
towards the posterior side of the patient.
How did the addition of wedges change the isodose distribution? Include a screen shot
(including axial and coronal) of the isodose distribution before and after the wedge
placement.
o The isodose lines expanded to cover more of the anterior portion of the PTV
because dose is being forced anteriorly by the wedge. I could tell when I had too
much of a wedge because I started to lose coverage posteriorly.
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Plan 6
Plan 6
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Plan 6
According to your Khan Physics book, what is the minimum distance a wedge or
absorber should be placed from the patient’s skin surface in order to keep the skin
dose below 50% of the dmax?
o 15 cm is the minimum distance it should be from the patient’s skin to keep the
skin dose below 50% of dmax.
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Plan 7: Insert an AP field with a 1 cm margin around the PTV. Remove any wedges that may
have been used. Calculate the four fields. At your discretion, adjust the weighting and/or
energy of the fields, and, if wedges will be used, determine which angle is best. Normalize your
final plan so that 95% of the PTV is receiving 100% of the dose. Discuss your plan rationale
with your preceptor and adjust it based on their input.
Embed a screen cap of your final plan’s isodose distributions in the axial, sagittal and
coronal views. Show the PTV and any OAR.
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Plan 7
Plan 7 Axial
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Plan 7 Coronal
Plan 7 Sagittal
Include a final DVH with PTV and OARs. Be sure to include clear labels on each image
(refer to the Canvas Clinical Lab module for clear expectations of how to format your
DVH).
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Use the table below to list typical organs at risk, critical planning objectives, and the
achieved outcome. Provide a reference for your planning objectives and a rationale
for the objectives chosen.
I used the ClearCheck application at my clinic to see if the OARs met the planning objectives. I
used a GI/Pelvis long course constraints template since the prescription is 45 Gy in 25 fractions.
In this case, the bladder and bowel did not meet the planning objectives because the PTV is
relatively large and it includes both of those structures in it. I’ve attached a copy of the
ClearCheck report that I ran to this assignment.
Organ at Risk (OAR) Planning Objective Objective Outcome Objective Met? (Y/N)
Bladder Mean≤4000-4400cGy Mean=4597.3cGy no
Rectum Max≤5440-5540cGy Max=4761.6cGy yes
Lt Femur D5%≤4500-5000cGy D5%=4363.9cGy yes
Bowel D120cc≤3500-3850cGy D120cc=4663.5cGy no