SBRT Flashcards

1
Q

SBRT meaning

A

Stereotactic Body Radiation therapy
Does not involve any stereotactic treatment to the brain

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Why SBRT

A

Dose escalation - targets in close proximity to OAR
Extra cranial
Around 1-5#
More than 8Gy per fraction
Highly conformal with steep gradients

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

SABR

A

Stereotactic ablative body Radiotherapy
Used for ablation - not many OARs surrounding
Extra cranial

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

SRS

A

Single fraction
For brain
Gamma knife is an example of SRS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

SRT

A

Stereotactic radiotherapy
Intra cranial
For larger lesions that are not suitable for SRS
Fractionated typically 2-5#

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Radiobiology in SBRT fractionation

A

Anti-tumour effects can not be predicted by classic radiobiology
Tumours may not be hypoxia therefore no benefit from reoxygenation
Hypo-fractionated alters micro environment which leads to more death of tumour cells
Dead tumour cells released quantities of antigens which stimulated antitumour immunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

The abscopal effect

A

Distant tumour regression after localised irradiation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What can we treat

A
  • inoperable tumours
  • oligometastic state
  • <5cm max dimension
  • non-malignant conditions
  • for ablation e.g. lung, liver
  • for dose escalation e.g. spine, prostate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Patient contraindications

A
  • prior RT
  • unable to lie flat
  • cannot receive chemo 1-4 weeks pre or post SBRT
  • severe connective tissue disease
  • claustrophobia
  • mental status prohibitive of patient compliance
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Average intensity profile versus maximum intensity profile

A

Maximum - sharper image
Average - more fuzzy, easier to match in treatment

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Image fusion issues

A

Image artefacts - from motion, metal implants
Image distortion - for PET and MR delineation
Registration errors - can be the largest source of error in the entire treatment process

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

SBRT techniques

A

Mohawk, flipper, seatbelt

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Dosimetry for SBRT

A

Always highly conformal
Inhomogenous dose distributions
170% max dose
Dose painting techniques

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Stereo dose distribution

A

Heterogenous
Fall off outside PTV 60-80%
PTV covered by 100% isodose

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Prescription

A

Prescribe at 80% iso line
Prescribe at an acceptable maximum point dose dose (e.g. 125%)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Plan evaluation priority

A

Check OAR goals - different OAR prescribed to conventional RT
Check PTV cover
Dose fall off beyond target

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

R50

A

Ratio of the volume covered by the isodose representing 50% of the prescription dose to the volume of the PTV

Function of the size of the PTV - smaller for large PTVs
This is volumetric not geographical

18
Q

Gradient index

A

Ratio of the volume of half the prescription isodose to the volume of the prescription isodose
Differentiates plans with similar conformity but with different gradients

19
Q

D2cm

A

The dose at any point at 2cm from the PTV is recorded and is expected to meet set criteria
Geographical evaluation

20
Q

Elekta hexapod

A

Patient immobilisation equipment must fit inside it
High sensitivity optical tracking

Difficulties
- must be positioned 30-50cm distance of iso
- arm position
- patient height
- patient BMI
- Indexing on vac bags

21
Q

When to use rotational corrections

A

Spine
Pancreas
For intercranial lesions, particularly if located at the base of the skull
For lesions abutting, overlapping with or within 2cm of critical normal tissue structures
For treating multiple lesions
Anything that is not round

22
Q

Motion management strategies

A

Breath hold
Elekta body fix
Compression belt and plate
Gating

23
Q

Sources of positional error

A

Resolution of imaging
Accuracy of image fusion
Accuracy of target delineation
Accuracy of mechanical iso
Accuracy of radiation/treatment iso
Resolution of couch positioning

24
Q

Sources of error - patient factors

A

Position
Immobilisation
Organ motion - respiration, cardiac function

25
Q

Level of accuracy

A

Dependent on sources of error and how they are managed
Dependent on clinical protocol (fractionation, margins, pathology)

26
Q

TPS technique

A

FFF - fast treatment
Collimator angle choice
VMAT - not ideal for single fraction due to leaf interplay

27
Q

MLC leaf interplay

A

Interaction between the movement of the MLC segments in VMAT or IMRT and the motion of a tumour with the respiration cycle
Best practice to plan on AV IP data set for dosimetry more representative of the total resp cycle

28
Q

Spine treatment

A

For oligometastatic disease
Very steep dose gradients around SC
Most commonly 1 vertebrae but can be multiple
PRV 1.5-3mm
Larger cord structures or the cal sac will impact PTV cover

29
Q

Lung patient conditions

A

Inoperable
Central (fractionate)
>5cm diameter
No tissue diagnosis
Salvage after prior RT
T3 tumour with chest wall invasion
Synchronous or multi-focal tumours

30
Q

Lung techniques

A

VMAT most common - except for single fraction regimes due to leaf interplay
Use FFF and DIBH

31
Q

Target delineation for lungs

A

ITV to be marked to encompass full range of tumour excursion
If using DIBH - do 2 CTs to check variability in breath holds

32
Q

When an OAR dose goal conflicts with covering iso lines, what happens

A

The dose to OAR and covering isodose should run like parallel or concentric

33
Q

Liver SBRT

A

Common site of Mets
For patients unsuitable for surgery
Can treat up to 5 lesions if Mets
Treats up to 3 lesions if HCC
Must have 800cc of uninvolved liver

34
Q

liver dose

A

48gy in 3
40-50Gy in 5
Lower dose used where there is underlying liver dysfunction

35
Q

Plan techniques for liver

A

Shorter arc lengths to avoid entry dose through liver
Partial arcs - slightly higher than mid range dose but lower low dose
Usually co-planar VMAT to avoid increasing low dose wash in liver

36
Q

Prostate SBRT

A

Mono therapy
As a boost
Requires fiduciary markers for accurate localisation
Space OAR needed

37
Q

Pancreas SBRT

A

Fidcucials useful
Use of oral contrast to distend duodenum
Critical structure. - duodenum
Very similar to liver protocol

38
Q

Desired accuracy

A

1mm 1 degrees

39
Q

Patient positioning considerations

A

Arm position
Comfortable and reproducible
Allow good access to target
Minimise dose to normal tissues
Minimise restriction on beam angle choice
Avoid creating build up with equipment
Consider head position, position of tubing for body fix, loc bars

Check whether patient comprehends and understands instructions

Pain control and management

Morbidity/co-morbidity

40
Q

What moves?

A
  1. Skeletal/muscular (i.e. the patient) – mitigate through stabilisation
  2. Respiratory motion – evaluate with 4DCT, manage with compression, breath hold or gating
  3. Cardiac motion – remains
  4. Peristalsis – manage with compression
  5. Bladder and bowel filling and emptying – manage with protocols,
    enemas, medications, catheterisation