GlD i tGel Dosimetry - American Association of … i tGel Dosimetry L..Jo Sc e e d Od g John...
Transcript of GlD i tGel Dosimetry - American Association of … i tGel Dosimetry L..Jo Sc e e d Od g John...
G l D i tGel Dosimetry L. John Schreiner and Tim Olding . Jo Sc e e d O d gCancer Centre of Southeastern Ontario
Queen’s University
DisclosureDisclosure
Schreiner, AAPM Colorado ‘09
Learning objectives
Introduce gel dosimetry
g j
• Introduce dosimeter systems• Readout systemsReadout systems• Fundamental mechanisms
Di li i l li iDiscuss clinical application• Preparation and Use • Show some examples of use
Schreiner, AAPM Colorado ‘09
Wh t is l d sim t r?What is a gel dosimeter?
Schreiner, AAPM Colorado ‘09
What is a gel dosimeter?
89 % bulk waterh 89 % bulk waterh
Small amount stuff 5 % gelatinSmall amount stuffthat changes under
irradiation
5 % gelatin
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irradiation
What is a Fricke gel dosimeter ?
89 % bulk waterh 89 % bulk waterh
5 % gelatinFe2+
F 3+ 5 % gelatinFe3+
(in FX gels, + 0.05 mM xylenol orange)
Schreiner, AAPM Colorado ‘09
What is a polymer gel dosimeter ?
89 % bulk waterh 89 % bulk waterh
monomers
5 % gelatin
monomers
l 5 % gelatinLarge polymers(in normoxic gels, + 5 mM tetrakis THPC)
Schreiner, AAPM Colorado ‘09
What is a gel dosimeter ?
hhChanges can be monitored by variousChanges can be monitored by various techniques and dose mapped in three dimensions
Small amount stuff
dimensions
Small amount stuffthat changes under
irradiation
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irradiation
So a gel dosimeter is a d system to capture dose
information in 3D
Yves DeDeene Ghent
CCSEO
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Schreiner, AAPM Colorado ‘09c/o Andrew Jirasek, U. Victoria, BC
Intrinsic energy dependence :Most investigations of polymer gels in proton
beams indicate the gels exhibit an LET dependencep
Schreiner, AAPM Colorado ‘09c/o Andrew Jirasek, U. Victoria, BC
Gel dosimetry
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Parker MSc 1997
Gel DosimetryyNot yet clinically adopted broadly
• Imaging for readout not always readily available (particularly the goldavailable (particularly the gold standard, MRI)
• Gel preparation (toxicity, oxygen contamination )contamination …)
• May have better tools for applicationsMay have better tools for applications tested to date
Dose Quantification
• Looking at the MR relationship gives a sense of the parameters defining the dose of the parameters defining the dose relationship
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• With substitution R1 = 1/T1
Dose Quantification
• Looking at the MR relationship gives a sense of the parameters defining the dose of the parameters defining the dose relationship
Schreiner, AAPM Colorado ‘09
• With substitution R1 = 1/T1
Dose Quantification
• Looking at the MR relationship gives a sense of the parameters defining the dose of the parameters defining the dose relationship
Schreiner, AAPM Colorado ‘09
• With substitution R1 = 1/T1
Dose Quantification
• Looking at the MR relationship gives a sense of the parameters defining the dose of the parameters defining the dose relationship
Schreiner, AAPM Colorado ‘09
• With substitution R1 = 1/T1
A busy slide: why we use calibrations
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Typical dose response
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MRIBased on change of NMR spin-relaxation rates in irradiated
dosimeter
Fricke gels R1 ( = 1/T1 )• Fricke gels - R1 ( = 1/T1 ) • polymer gels – R2 (= 1/T2 ) or magnetization transfer imaging
Schieb 2001 BANG gel Crooks 1994 Fricke gel
AsideWhat is the accuracy and precision of gel dosimetry
• Relative doses - 3%, <2% easily in our workDelivered dose (absolute dose) 5% easily 3% with some work• Delivered dose (absolute dose) – 5% easily, 3% with some work
Schieb 2001 BANG gel Crooks 1994 Fricke gel
x-ray CT Based on change of density in irradiatedpolymer gel dosimeters
ypolymer gel dosimeters
Hilts et al. PMB 2000 PAGNIPAM with glycerol
PAG
Jirasek et al PMB 2009Jirasek et al. PMB 2009
B d h f ti l tt tiOptical CT
Based on change of optical attenuation coefficients in irradiated dosimeter
• Fricke gels - Absorption changes
p
g p g
• polymer gels – mainly changes in scatter
Optical CT Modus Medical CBCT optical systemp
FX gelFX gel
Optical CT0.15
m-1
)p0.1
uatio
n (c
m
5 cm9 cm
0
0.05
Atte
nu
2 cm
00 50 100
Position (mm)0.4-1
)
y = 0.9213x
0.3
Coe
ffici
ent (
cm-
0.1
0.2
sta
Atte
nuat
ion
Uncorrected Scatter SolutionsBSA CorrectedDye SolutionsFan BeamLi Fit (BSA C t d)
CBCT optical system
00 0.2 0.4 0.6 0.8 1 1.2
Spectrophotometer Attenuation Coefficient (cm-1)
Vis Linear Fit (BSA Corrected)
Timescale for Gel dosimetry (typical times and limits)
Prepare IrradiateFricke
Wait( bring to
r dnFricke systems
45 minNIPAM (polymer)
Fricke<20 minPolymer
12 hrs to 1 weekPolymer
12 hrs to 1 week
radn
room T )
45 minym
No limit( dark cool storage )
3 4 hAnalysis Readout
Fricke
Wait
3-4 hrsCalibration, registration,
l i (
OpticalCBCT < 8 +10 min
2nd gen CT > 30 min 1 hrMRI
30 min – 2 hour (maybe )Polymer
> 12 (24) hrsanalysis (gamma maps DVHs etc)
MRI30 min 1 hr f (readout)
( MRI may be more sensitive )
Timescale for Gel dosimetry (typical times and limits)
Prepare IrradiateFricke
Wait( bring to
r dnFricke systems
45 minNIPAM (polymer)
Fricke<20 minPolymer
12 hrs to 1 weekPolymer
12 hrs to 1 week
radn
room T )
45 minym
No limit( dark cool storage )
3 4 hAnalysis Readout
Fricke
Wait
3-4 hrsCalibration, registration,
l i (
30 min – 2 hour (maybe )Polymer
> 12 (24) hrsanalysis (gamma maps DVhs etc) f (readout)
( MRI may be more sensitive )NIPAM added at too high T
Timescale for Gel dosimetry (typical times and limits)
Prepare IrradiateFricke
Wait( bring to
r dnFricke systems
45 minNIPAM (polymer)
Fricke<20 minPolymer
12 hrs to 1 weekPolymer
12 hrs to 1 week
radn
room T )
45 minym
No limit( dark cool storage )
( dark cool storage )
3 4 hAnalysis Readout
Fricke
Waitstorage )
3-4 hrsCalibration, registration,
l i (
OpticalCBCT < 8 +10 min
2nd gen CT > 30 min 1 hrMRI
30 min – 2 hour (maybe )Polymer
> 12 (24) hrsanalysis (gamma maps DVhs etc)
MRI30 min 1 hr f (readout)
( MRI may be more sensitive )
Timescale for Gel dosimetry (typical times and limits)
Prepare IrradiateFricke
Wait( bring to
r dn• Calibration Fricke systems
45 minNIPAM (polymer)
Fricke<20 minPolymer
12 hrs to 1 weekPolymer
12 hrs to 1 week
radn
room T )
• Choice of gel and readout system45 min
ymNo limit( dark cool
storage )
g y
3 4 hAnalysis
Fricke
WaitReadout
3-4 hrsCalibration, registration,
l i (
30 min – 2 hour (maybe )Polymer
> 12 (24) hrs
OpticalCBCT < 8 +10 min
2nd gen CT > 30 min - 1 hrMRI
( bring to measurement
room T )analysis (gamma maps DVHs etc) f (readout)
( MRI may be more sensitive )
MRI30 min / 1 hr
room T )
CALIBRATION
vialsInternal
vials
Independent from same batch
Gel Dosimetryy
Will i s li ti s llWill now review some applications wellsuited to gels
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Application 1: Beam commissioning of small fieldssmall fields
Moutsatsos et al., Dosgel’08
Pappas et al., Dosgel’08
Petrokokkinos et al., D l’08Dosgel’08
Application 2: Commissioning of t h i i th li i
Fricke Gel IMRT Validation
new techniques in the clinic
Fricke Gel IMRT Validation
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200 cGy Eclipse Plan OptCT Measurement
IMRT Gamma Evaluation
Gamma 3% 3mm
(93% of dosimeter i l d)pixels passed)
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Application 2b: Commissioning of new techniquestechniques
Ceberg et al., Dosgel’08
PAGAT gel dosimeter with MRIPAGAT gel dosimeter with MRI readout at 1.5 T using multiecho T2 sequence (TE 25 ms, TR 4000 ms) ,
3voxel size 1x1x3 mm3
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Schreiner, AAPM Colorado ‘09
Application 3: Adaptive Radiation Therapy Process QATherapy Process QA
A proposalA proposal
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Image Guided Ad ti R di ti
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Adaptive Radiation Therapy
1) These are all intricate processes with complex data transfer between points, also requirin human evaluation and human
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also requiring human evaluation and human intervention.
Could use a test tool that mimics a patient undergoing treatment
5 & 65 & 6
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8
Physicists / physics team / rad oncs
4
90
2
Dose (Gy)
EvaluationSchreiner, AAPM Colorado ‘09
Evaluation
Jar Volume
100 EclipseGel
Bladder
100Example con’t
25
50
75
Frac
tion
of V
olum
e (%
) Gel
25
50
75
Frac
tion
of V
olum
e (%
)
00 2 4 6
Dose (Gy)
00 2 4 6
Dose (Gy) Rectum
100
%)
Prostate
100
%)
0
25
50
75
Frac
tion
of V
olum
e (%
0
25
50
75
Frac
tion
of V
olum
e (%
00 2 4 6
Dose (Gy)
00 2 4 6
Dose (Gy) Prostate + 1.5cm (Control Volume)
75
100m
e (%
)Cumulative GVH
0
25
50
0 2 4 6
Frac
tion
of V
olum
(gamma test)
Schreiner, AAPM Colorado ‘09
Dose (Gy)
Jar Volume
100 EclipseGel
Bladder
100Example con’t
25
50
75
Frac
tion
of V
olum
e (%
) Gel
25
50
75
Frac
tion
of V
olum
e (%
)
00 2 4 6
Dose (Gy)
00 2 4 6
Dose (Gy) Rectum
100
%)
Prostate
100
%) OOPs
0
25
50
75
Frac
tion
of V
olum
e (%
0
25
50
75
Frac
tion
of V
olum
e (% OOPs
00 2 4 6
Dose (Gy)
00 2 4 6
Dose (Gy) Prostate + 1.5cm (Control Volume)
75
100m
e (%
)Cumulative GVH
0
25
50
0 2 4 6
Frac
tion
of V
olum
(gamma test)
Schreiner, AAPM Colorado ‘09
Dose (Gy)
Conclusions• Many of the problems that have kept gel dosimetry
out of the clinic have been corrected
• Gels have some special roles:p– Small beam commissioning
Validation of new techniques (particularly before using– Validation of new techniques (particularly before using and external credentialing service, e.g., RPC)
P h h i l i RT P QA• Perhaps have a unique role in RT Process QA
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ConclusionsConclusions
C d i• Care and consistency
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Ideal Dosimeter: makes for well planned, smooth and easy route to a l d d ti tiplanned destination.
Clinical Dosimeters: trip may not be as smooth and may require a bit more skill but with careful use of skills and technique destination can be reached.
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DosGel Conferences on Radiotherapy Gel DosimetryDosimetry.
(2004, 06 and 08 proceedings available on web through J Phys Conf Series)J Phys Conf Series)
Acknowledgementsg• Graduate Students: (current and long previous)
Matthew Podgorsak, Chantal Audet, Brian Keller, WillMatthew Podgorsak, Chantal Audet, Brian Keller, Will Parker, Rob Senden, Adrian Fuxman, Valeria Koeva, Oliver Holmes, Tim Olding,
• Dosgelers: Kim McAuley, Simon Doran, Geoff Ibbott, Yves Dedeene, Mark Oldham, Evangelos Pappas, Thomas Maris, Sophie Ceberg, Michele Hilts, Sven Bäck, Andrew Jirasek, Clive Baldock and othersAndrew Jirasek, Clive Baldock and others
Schreiner, AAPM Colorado ‘09