Evaluation of a new VMAT QA device, or the "X" and "O" array geometries

被引:109
作者
Feygelman, Vladimir [1 ]
Zhang, Geoffrey [1 ]
Stevens, Craig [1 ]
Nelms, Benjamin E. [2 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Div Radiat Oncol, Tampa, FL 33612 USA
[2] Canis Lupus LLC, Sauk Cty, WI 53561 USA
关键词
IMRT QA; rotational therapy; dose distribution comparison; three-dimensional dosimetry; diode array; MODULATED RADIATION-THERAPY; IONIZATION-CHAMBER ARRAYS; IMRT QUALITY-ASSURANCE; DIODE-ARRAY; ARC THERAPY; DOSIMETRIC EVALUATION; RADIOGRAPHIC FILM; POLYMER GEL; ION-CHAMBER; VERIFICATION;
D O I
10.1120/jacmp.v12i2.3346
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
We introduce a logical process of three distinct phases to begin the evaluation of a new 3D dosimetry array. The array under investigation is a hollow cylinder phantom with diode detectors fixed in a helical shell forming an "O" axial detector cross section (ArcCHECK), with comparisons drawn to a previously studied 3D array with diodes fixed in two crossing planes forming an "X" axial cross section (Delta(4)). Phase I testing of the ArcCHECK establishes: robust relative calibration (response equalization) of the individual detectors, minor field size dependency of response not present in a 2D predecessor, and uncorrected angular response dependence in the axial plane. Phase II testing reveals vast differences between the two devices when studying fixed-width full circle arcs. These differences are primarily due to arc discretization by the TPS that produces low passing rates for the peripheral detectors of the ArcCHECK, but high passing rates for the Delta(4). Similar, although less pronounced, effects are seen for the test VMAT plans modeled after the AAPM TG119 report. The very different 3D detector locations of the two devices, along with the knock-on effect of different percent normalization strategies, prove that the analysis results from the devices are distinct and noninterchangeable; they are truly measuring different things. The value of what each device measures, namely their correlation with - or ability to predict - clinically relevant errors in calculation and/or delivery of dose is the subject of future Phase III work.
引用
收藏
页码:146 / 168
页数:23
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