TSET
TG-30
Introduction Requirements Techniques LINAC Operating Conditions Dosimetry and Instrumentation Patient Considerations
Introduction to TSET
Diseases most commonly treated (require shallow Tx depths)
Cutaneous T-cell Lymphomas
Micosis Fungoides Sezary syndrome (less so than Micosis Fungoides)
Requirements
Beam
Specification of:
Field size, penetration, energy, depth, dose rate, field flatness in treatment plane, X-ray background, and the need and nature of boost fields
Room
Careful consideration of:
Space, shielding, ventilation, electron ranges
Beam Requirements
Field size 200 cm high by 80 cm wide Penetration depth Varies with stage, type of disease, and over the body surface Typically 5 15mm or more at the 50% isodose line Energy 3 to 7 MeV at patient treatment plane 4 to 10 MeV at beam exit window Dose rate In order to reduce Tx time high dose rates are desirable Range from 0.25 Gy/min to several Gy/min
Beam Requirements
Field flatness in the treatment plane Vertical uniformity of +-8%, Horizontal Uniformity of +-4% over the central 160 cm x 60 cm area X-ray background Penetrating and forward directed Exposes most of body and should be ALARA Can be reduced by angling beams such that the x-ray peaks lie outside the body Desired to be 1% or less averaged over the entire body (typically 1-4%) EORTC spec < 5% Need and nature of boost fields Some body areas are unintentionally shielded by other body sections or inadequately exposed due to limitations of beam geometry
Profiles
Left: 6E 10x10 surface Right: 6E HDTSE (no cone, 10x10 XY jaws)
Room Requirements
Space
In order to provide good dose uniformity large distances are needed Typically 2-7m from scatterer and patient (depending on technique)
Ventilation
TSET involves significant ozone production from ionizing large volumes of air in the treatment room Frequent exchange of air is essential for confining ozone exposure
Shielding
Typically MV X-ray shielding is adequate, but should measure Electron Ranges
Max track length range of ~0.5 g/cm2 per MeV (~4 m/MeV) in air Range is typically not in direction of beam, most stop far short of this
Bremsstrahlung
Techniques
Why do we need special techniques, are large AP/PA fields not sufficient?
No, they are not sufficient:
Patients body shape is not flat Dose uniformity impossible with AP/PA
Techniques
Techniques
How do you treat curved surfaces?
Multiple fields Electron arcs
Techniques
Prior to use of LINACs
Beta Particles
Beta-particle beams used Sr/Y-90 with Emax=2.18 MeV Use 10% isodose line and deliver 2Gy/fx in 15 min fx by scannins over a patient surface 60 cm x 180 cm
Techniques
Used with LINACs
Scattered single beam
6.5 MeV beam with 0.15mm thick titanium scattering foil placed 10 cm from accelerator window Shaped polystryrene beam-flattening filter mounted on front of treatment head Producing a flattened 4 MeV beam at the Tx plane
Stanford Technique
Most commonly used technique Utilizes 6 dual fields
Each dual field is comprised of two angled beams
Typically 18 to 20 from 270 or 90 gantry position
Stanford Technique
Stanford Technique
Stanford Technique
Techniques
Used with LINACs
Pendulum-arc
8 MeV beam with the gantry rotated continuously during treatment in a 50 arc (six fields) Arc starts from an initial angle with CAX above the head and ends with CAX below the feet Degrader: large 1 cm thick plexiglass sheet 5cm from the patient Provides large angle electron scattering near the patient
Patient Rotation
Use single horizontal 6 MeV beam (3.5 MeV at Tx plane) with a scatterer near the exit window and a 7 m treatment distance X-ray background = 2.2% Reduced setup and Tx times as well as simplified beam matching Self shielding by limbs is unavoidable
Pendulum Arc
Patient Rotation
High average beam current (100 times normal electron beam) for high dose rate (>1Gy/min) at Tx plane
X-ray background is least when scattererdegrader is close to patient (~15mm from pt)
Should be placed where beam exits accelerator A common combination for TSET monitoring:
a full-beam transmission ionization chamber at or within the treatment head a sampling chamber or electron collector placed at or near the patient Tx plane but not in line with the patient
Ion chambers (small thimble or small volume/thin window p-p) are recommended for scanning in a water tank If film is used with solid water, no air gaps should be present
Might be difficult if film is in a package
Phantoms
Square water phantoms are recommended for depth dose data Otherwise, layered, flat phantoms made of conducting plastics or thin laminae of polystyrene with conductive graphite coatings are recommended for depth dose and buildup data Elliptical, oval or cylindrical phantoms are recommended for simulating a patients body
Fluence
Evacuated Faraday cup with collimator placed over the aperture Electron fluence is determined from the charge collected and the area of the collimator This fluence can be used to estimate entrance surface dose
Depth dose
Using a parallel-plate chamber overlayed with varying thicknesses of polystyrene EORTC: R80 > 4mm, R20 < 2cm
Patient Considerations
Positioning
Patient should be positioned to minimize self shielding
Support devices
Patients may have trouble standing Should be prepared with multiple alternative positioning methods
Shielding
Lenses of the eyes can be shielded by placing high Z material either over or under the eye lids Finger and toe nails can be shielded with thin sheets of lead cut to size
Shielding
Patient Considerations
Boost Fields
Typically the Soles of the feet, the perineal area, the dorsal surface of the penis, peri-anal skin, and the inframammary region of large breasted women Areas requiring a boost are determined by in-vivo dosimetry
Boost Fields
Commissioning
LINAC must be capable Room must be large enough Determine a Beam monitoring approach Decide on a technique Build or purchase patient support system Create a written procedure for changing from conventional modalities to TSET and back to conventional Determine an In-vivo dosimetry protocol
TSET at MDACCO
IX Vault Patient Support System Stanford Technique In-Vivo Dosimetry system
Independent of energy for 6 and 18 MV beams Response increases linearly with dose rate Time resolution = 0.1s, Spatial resolution <0.5mm Readings compare well with TPS calculations
Review
What is TSET e- beam energy?
Nominal? 9 MeV At pt surface? 4 MeV
What are differences between clinical e- beam and TSET beam? Higher dose rates; Larger Field Sizes; No Cones What are common Tx indications for TSET?
T-cell Lymphoma (micosis fungoides) Doses? 36Gy in 9 fx