3D Diode Array Commissioning: Building Confidence in 3D QA Technology Caroline Yount, MS CANCER CENTER
3D QA The complex three-dimensional (3D) shapes of intensity modulated radiation therapy (IMRT) dose distributions and the methods for IMRT dose delivery demand that the dosimetry measurement techniques be reviewed and adapted for the unique challenges posed by IMRT. TG 120
QA Challenges Modern technologies are utilizing rotation delivery to speed up treatment time and decrease tissue toxicity (RapidArc, VMAT, TomoTherapy, IMAT, SmartArc) Rotational beam delivery creates a challenge for patient specific QA 360 degrees of delivery
3D QA
3D QA
3D QA
3D QA
ArcCHECK Introduction Designed for Helical & Arc Delivery 1386 diodes in a helical geometry 21cm diameter, 21cm length 1cm spacing, 3.28cm equivalent depth 0.64mm 2 active detector area 4 th Dimension = Time 50ms update frequency Optional cavity plug insert with ion chamber holder PMMA construction
Detector Geometry Entrance and exit dose are measured Effectively doubling the detector density in the measurement field. Central 10x10 contains approximately 230 detectors Detectors are arranged on a HeliGrid Increases sampling rate and reduces detector overlap from Beams Eye View (BEV) Entrance and exit dose can be correlated to determine gantry angle
Question How can I interpret and trust 3D QA?
Commissioning Measurements 1. Detector spacing 2. Linearity 3. Sensitivity 4. Individual detector response variations 5. Absolute dose accuracy Then Trend analysis
Detector spacing kvct MVCT
Linearity Conventional Dose Rates Dose @ a central diode 0 500 1000 1500 2000 2500 3000 200 300400 500 600700 800 1000 R² = 1 2000 0 500 1000 1500 2000 2500 MU Reading/MU 1.00 1.05 1.10 1.15 1.20 1.25 6MV 500MU/min 10x10 100SAD Ratio 0 1000 2000 3000 MU
Linearity High Dose Rates Dose @ a central diode 0 1000 2000 3000 4000 5000 1000 2000 R² = 1 4000 500 50 0 1000 2000 3000 4000 5000 Reading/MU 1.00 1.05 1.10 1.15 1.20 1.25 6MV FFF 1400MU/min 10x10 100SAD Ratio 0 2000 4000 6000 MU MU
Linearity High Dose Rates Dose @ a central diode 0 1000 2000 3000 4000 5000 6000 1000 2000 R² = 1 4000 500 50 0 1000 2000 3000 4000 5000 MU Reading/MU 1.00 1.10 1.20 1.30 10MV FFF 2400MU/min 10x10 100SAD Ratio 0 2000 4000 6000 MU
Spatial Sensitivity Table = 0mm Table shifted laterally = 0.5mm
Spatial Sensitivity Lateral Table Shifts 0.5mm 1mm 2mm 98% 96% 94% 92% 90% 88% 86% Pass Rate vs Shift 0 1 2 3 4 Shift (mm) 3mm
Spatial Sensitivity Longitudinal Table Shifts 0.5mm 1mm 2mm 98% 96% 94% 92% 90% 88% 86% Pass Rate vs Shift 0 1 2 3 Shift (mm) 3mm
Angular Sensitivity Gantry Angle Changes 0.5 1 2 98% 96% 94% 92% 90% 88% 86% Pass Rate vs Angle Change 0 1 2 3 Change in Angle (degrees) 3
Detector Response Variations Sensitivity differences between the ArcCHECK detectors These differences can be measured Individual correction factors applied to subsequent raw measurements
Detector Response Variations
Detector Response Variations
Calibration Validity Check AP PA
Calibration Validity Check Factory array calibration: In house array calibration:
Calibration Validity Check New In house array calibration: 1% 1.5%
ArcCHECK Calibration Array calibration on standard linac Dose calibration on standard linac SAD hand calc at 3.28 cm depth (water equivalent depth)
Dose Accuracy Measured 10x10 Planned 10x10
Clinical Example Chest
Phantom Plan
QA Result Measured Calculated Comparison Ion Chamber = -2% Profiles
Clinical Example Head & Neck
Phantom Plan
QA Result Measured Calculated Ion Chamber = 0% Comparison Profiles
Clinical Example Prostate
Phantom Plan
QA Result Measured Calculated Ion Chamber = -1.2% Comparison Profiles
Trend Analysis When did 3D QA indicate clinical issues?
Trend Analysis Patient specific Chamber Readings 13.5% 12.0% 10.5% 9.0% 7.5% 6.0% 4.5% 3.0% 1.5% 0.0% 1.5% 3.0% 4.5% 6.0% 7.5% 9.0% 10.5% 12.0% 13.5% Machine dose rate low ~900 QAs Setup error, high gradients, modulation too high
Trend Analysis Patient specific Gamma Pass Rates 70% Last 100 QAs 60% 50% 40% 30% 20% 10% 0% Gamma 3%/3mm <1
Future work 1. Better characterization with FFF 2. Higher resolution characterization for SRS 3. Applying results to patient s CT for DVH analysis
Conclusions 1. Commissioning 2. Ongoing Quality Improvement
Thank you!