Dosimetric evaluation of Acuros XB Advanced Dose Calculation algorithm in heterogeneous media
 Antonella Fogliata^{1}Email author,
 Giorgia Nicolini^{1},
 Alessandro Clivio^{1},
 Eugenio Vanetti^{1} and
 Luca Cozzi^{1}
https://doi.org/10.1186/1748717X682
© Fogliata et al; licensee BioMed Central Ltd. 2011
Received: 23 May 2011
Accepted: 19 July 2011
Published: 19 July 2011
Abstract
Background
A study was realised to evaluate and determine relative figures of merit of a new algorithm for photon dose calculation when applied to inhomogeneous media.
Methods
The new Acuros XB algorithm implemented in the Varian Eclipse treatment planning system was compared against a Monte Carlo method (VMC++), and the Analytical Anisotropic Algorithm (AAA). The study was carried out in virtual phantoms characterized by simple geometrical structures. An insert of different material and density was included in a phantom built of skeletalmuscle and HU = 0 (setting "A"): Normal Lung (lung, 0.198 g/cm^{3}); Light Lung (lung, 0.035 g/cm^{3}); Bone (bone, 1.798 g/cm^{3}); another phantom (setting "B") was built of adipose material and including thin layers of bone (1.85 g/cm^{3}), adipose (0.92 g/cm^{3}), cartilage (1.4745 g/cm^{3}), air (0.0012 g/cm^{3}). Investigations were performed for 6 and 15 MV photon beams, and for a large (13 × 13 cm^{2}) and a small (2.8 × 13 cm^{2}) field.
Results
Results are provided in terms of depth dose curves, transverse profiles and Gamma analysis (3 mm/3% and 2 mm/2% distance to agreement/dose difference criteria) in planes parallel to the beam central axis; Monte Carlo simulations were assumed as reference. Acuros XB gave an average gamma agreement, with a 3 mm/3% criteria, of 100%, 86% and 100% for Normal Lung, Light Lung and Bone settings, respectively, and dose to medium calculations. The same figures were 86%, 11% and 100% for AAA, where only dose rescaled to water calculations are possible.
Conclusions
In conclusion, Acuros XB algorithm provides a valid and accurate alternative to Monte Carlo calculations for heterogeneity management.
Keywords
Background
A new photon dose calculation algorithm has recently been implemented in the Eclipse treatment planning system (Varian Medical Systems, Palo Alto, USA). This algorithm, named Acuros^{®} XB Advanced Dose Calculation (Acuros XB in the following) belongs to the class of the Linear Boltzmann Transport Equation (LBTE) Solvers. LBTE solvers, similarly to those used in Monte Carlo methods, aim to allow for accurate modelling of dose deposition in media.
Many studies explored the accuracy of algorithms for photon dose calculation in materials different from water. In 2006 a classification was proposed dividing algorithms into "type a" and "type b" groups (Knöös et al [1]), according to management (type b) or non management (type a) of the electron transport in dose calculation. "Type b" algorithms present higher accuracy in heterogeneous media, in particular for very low density tissues [2]. The differences observed in phantom studies are partially mitigated in patients, where there is a predominance of soft tissues, more similar to water [1]; in cases with large volumes of air or low density media the differences remained largely in favour of "type b" models [3].
Many studies have also been published to compare different algorithms with Monte Carlo simulations or measurements: the Anisotropic Analytical Algorithm (AAA) was evaluated e.g. by van Esch [4], Fogliata [2], daRosa [5]. Results showed that accuracy significantly depends on energy, field size, and density of the materials. Algorithms allowing calculation of dosetomedium lead to better agreement with Monte Carlo as already shown by Siebers [6] and confirmed by Knöös [1]. The clinical applicability of dosetomedium calculations is limited to few systems and the new Acuros XB is included in this list. The first works on validation and evaluation of the Acuros XB algorithm were recently published by Fogliata et al[7] and Bush et al[8] showing very promising results compared to both measurements and Monte Carlo calculations.
The present report summarises a study conducted to investigate the performance and accuracy of the Acuros XB in its Eclipse implementation, when applied to materials different from water. Tests are performed in simple geometrical phantoms with inserts or layers of different materials for photon beams. Acuros XB calculations are performed using both dosetomedium and dosetowater options. The validation assumes, as benchmark, Voxel Monte Carlo (VMC++) simulations. To complete the comparative analysis, results are reported also for the latest version of the AAA, the "type b" algorithm currently implemented in the Eclipse TPS.
Methods
The algorithms
The Acuros XB Advanced Dose Calculation algorithm
The Acuros XB is based on the application of the LBTE that describes the interactions of radiation particles with matter. This is based on approximate numerical methods. Monte Carlo (MC) and explicit LBTE solvers, as Acuros XB, should converge to the same final results. In practice, both methods are affected by potential inaccuracies depending on the level of sampling of the probability distribution functions applied during MC simulations or to the application of variables discretisation during explicit LBTE solution. A characteristic of LBTE solvers, compared to MC simulations, is the absence of uncertainties due to statistical noise in the calculated dose.
Progenitor of Acuros is the Attila algorithm [9], developed originally for nuclear physics applications, and also investigated for external photon beam dose calculations [10, 11] and brachytherapy [12]. The new Acuros algorithm, based on many of the Attila methods, was adapted for external photon dose calculations and described in Vassiliev et al[13]. Acuros XB is the Varian implementation in the Eclipse planning system of the original Acuros algorithm.
Acuros XB implementation consists of two main components: i) the photon beam source model and ii) the radiation transport model.
The latter includes discretisation of the spatial ( ), energy (E), and angular ( ) variables and was firstly described by Vassiliev et al[13] and summarised in a previous report on Acuros XB validation in water for simple fields [14].
where σ^{e}_{ED} is the macroscopic electron energy deposition cross section, ρ the material density, and Ψ^{ e }the angular electron fluence. Acuros XB calculates the energy dependent electron fluence, based on the material properties of the patient, as derived from the Hounsfield Unit (HU) of the CT dataset.
Dose to medium or dose to water can be selected in Acuros XB.
When dose to medium is calculated, σ_{ED}^{e} and ρ and are based on the material properties of output grid voxel, i.
When dose to water is reported, σ_{ED}^{e} and ρ are based on water in a post processing step (the transport calculation is identical for both dose to medium and dose to water reporting); in materials different from water, the dose is defined as the dose absorbed by a volume of water which is small enough not to perturb the energy dependent electron fluence. This volume should be much smaller than the output dose grid voxel of the computer based calculation or of any detector used to measure dose to water.
where M is the atomic mass and N_{ α }is the Avogadro's number. Coupled photonelectron cross sections include Compton scatter, photoelectric effect, and pair production, but not the Rayleigh scatter. In the model, the energy from bremsstrahlung photons produced by electron interactions inside the patients is not considered, being judged not significant for energies typical in the radiotherapy range.
The cutoff for electron energy is set at 500 keV (200 keV in version 11) kinetic energy only (without rest mass) and it is not modifiable by the user.
Material mass densities for automatic conversion, as implemented in the two Acuros XB versions.
Material  Density Range [g/cm^{3}] Acuros XB version 10  Density Range [g/cm^{3}] Acuros XB version 11 

Air    0.0000.020 
Lung  0.0000.590  0.0110.624 
Adipose Tissue  0.5900.985  0.5541.001 
Muscle, Skeletal  0.9851.075  0.9691.093 
Cartilage  1.0751.475  1.0561.600 
Bone  1.4753.000  1.1003.000 
The Anisotropic Analytical Algorithm, AAA
Comparison to the AAA algorithms was also included in the study. AAA, based on the work of Ulmer et al [16–18] and Tillikainen et al [19, 20], was extensively validated [2, 4, 21–26]. The reader should refer to Tillikainen et al [20] for detailed description. AAA is not accounting for chemical material/tissue properties, hence the computed dose can be defined as dose to water, rescaled according to the specific density (dose rescaled to water in the following).
The Voxel Monte Carlo, VMC++
The Voxel Monte Carlo VMC++ [27–30] is a class II condensed history Monte Carlo simulation of coupled electronphoton transport. It uses small angle approximation, and reuses electron histories and STOPS (Simultaneous Transport Of Particle Sets) variance reduction techniques [31]. It was validated in the field of radiotherapy by Gardner et al [32].
The version of VMC++ used here is implemented as a research version in Eclipse. Material chemical composition and related density ranges are here set identical to the Acuros XB settings. For the simulations, the electron energy cutoff is automatically selected and based upon the density of the material density; a smoothing process is activated during calculations (locally adaptive SavitzkyGolay filter); final dose calculation accuracy is set to 1%. A cross validation of VMC++ version is here presented against EGSnrc as already published [2]. During EGSnrc simulations 75 million particles are used to have a maximum statistical uncertainty of about 2%. The resolution is 2.5 mm in all directions. The total energy cutoff for electrons and photons are set to 700 keV and 10 keV, respectively.
Source model
The source model used for this study is the standard multiple source implemented in Eclipse and is the same for all algorithms used: Acuros XB, AAA and VMC++. For a detailed description the reader can refer to Tillikainen et al [19].
Eclipse framework and tested versions
All calculations are performed using the Eclipse planning system, with version 10 for Acuros XB and AAA, and version 8 for VMC++. The algorithm versions used are as following:

Acuros XB: clinical release 10.0.28.

AAA: clinical release 10.0.25.

VMC++: research release 8.0.1, not for clinical usage.
Some results are also reported for the Acuros XB calculations in its engineering preclinical version 11.0.03. Two are the main differences between the two Acuros XB versions 10 and 11. The first concerns the human material assignment, where the Air material is assigned to very low density regions in the body (Air material is not present in version 10), and the density ranges for each material are slightly overlapping (Table 1). The second improvement refers to a better resampling process of the structure voxels to the calculation grid, setting the density and material of the structure to the calculation voxel when at least half of the calculation voxel volume belongs to the structure.
All calculations, are performed with a grid size of 1.25 mm. The grid, in addition to the smoothing process used in the VMC++ calculations might lead to some unavoidable smoother dose profiles.
The phantoms and the beams
All studies are performed on a set of virtual phantoms.

Normal Lung: 0.198 g/cm^{3}, HU = 780, lung tissue, 16 cm thick.

Light Lung: 0.035 g/cm^{3}, HU = 942, lung tissue, 16 cm thick.

Bone: 1.798 g/cm^{3}, HU = 1380, bone tissue, 6 cm thick.

Layer A: 1.4751 g/cm^{3}, HU = 763, bone tissue, 1 cm thick

Layer B: 0.0012 g/cm^{3}, HU = 993, air, 1.6 cm thick

Layer C: 0.92 g/cm^{3}, HU = 122, adipose tissue, 2 cm thick

Layer D: 1.4745 g/cm^{3}, HU = 762, cartilage tissue, 1 cm thick.
Notice that layers A and D differ for only one HU, but have different material assignment (bone or cartilage), presenting different elemental composition, especially in terms of Calcium content.

field sizes: 2.8 × 13 cm^{2}, small field, SF, (the long axis crossed the heterogeneity boundary), and 13 × 13 cm^{2}, large field, LF.

beam energies: 6 and 15 MV from a Varian Clinac 2100 iX, presenting TPR_{20/10} of 0.672 and 0.761 respectively (6X and 15X in the following).
For all cases, calculations are performed for Acuros XB and VMC++ as: i) dose to water, ii) dose to medium and iii) dose rescaled to water. This last modality is defined with a manual assignment to water material for all phantom structures, outline and inserts, with specific HU according to each phantom setting; CT ranges to corresponding materials and compositions are modified accordingly also for VMC++ calculations. For AAA, only the dose rescaled to water option is available.
The analysis
1D analysis: DD and profiles
Data are reported for calculations along the directions shown by the arrows in figure 1, i.e. depth dose curves (DD) at 4 cm offaxis parallel to the beam central axis for phantom A, and on the beam central axis for phantom B.
Horizontal transverse profiles are calculated at the depth of midthickness of the inhomogeneities for phantom A to evaluate the lateral interface.
2D analysis: Gamma evaluation

pre: before the inhomogeneity, from 3 cm depth, with 1.5 cm internal margin from the field edge on the left and the beam central axis on the right

in: inside the inhomogeneity, with the same lateral margins of 1.5 cm

post: after the inhomogeneity for a depth of 2 cm.

edge: along the inhomogeneity, across the field edge, 1.5 cm inside and 1.5 cm outside the border

edge_in: the edge sector only inside the field

edge_out: the edge sector only outside the field

axis: across the beam central axis (and also inhomogeneity), 1.5 cm inside and 1.5 cm outside the inhomogeneity

axis_in: the axis sector only inside the inhomogeneity

axis_out: the axis sector only outside the inhomogeneity
Gamma evaluation is recorded as Gamma Agreement Index, GAI, defined as the percentage of the pixels fulfilling the criteria inside each sector.

pre: before the first inhomogeneity, from 3 to 5 cm depth

bone: inside the bone layer of 1 cm

air: inside the air layer of 1.6 cm

adipose: inside the adipose layer of 2 cm

cartilage: inside the cartilage layer of 1 cm

post: after the last inhomogeneity layer, for 2 cm depth.
Results and Discussion
Dose to medium, dose to water, dose rescaled to water
The Lung cases present very small differences among all calculation modalities. In the Bone case, dose to water calculations in bone show strong difference in DD compared to the other two calculations. Dose to medium is expressed as dose to water multiplied by the stopping power ratio s_{ water,medium }between the two media; s_{ water,bone }is in the range 1.091.15 for cortical bone [6]. This confirms the difference of ~1014% reported here. From a qualitative analysis of the Bone DD, a small peak about 23 mm before and behind the insert is computed in the dose to medium with Acuros XB. Small peaks in the dose to medium calculations are consistently present also in the horizontal profiles at the level of the interface between the two media.
Phantom B data show similar patterns depending on the layer material, with enhanced criticalities due to the short distance between interfaces and to the presence of different adjacent materials with very different density and composition, e.g. bone and air, where the different exit dose from bone is reflected in higher dose inaccuracy in the next air layer.
VMC++ vs. EGSnrc comparison
Onedimensional analysis: DD and profiles
In the following, only graphs relative to dose to medium calculations for Acuros XB, AAA and VMC++ are presented. Graphs referring to dose to water and dose rescaled to water are reported as additional files.
For all calculations performed in Normal Lung tissue, good agreement between Acuros XB and VMC++ is achieved. AAA, as expected from the radiation transport model, is less accurate especially for small fields and high energy beams [2]. The rebuildup curve behind the low density insert starts at the interface layer in Acuros XB calculations, while in VMC++ computations it starts about 1 mm inside the lung insert. This effect, more evident for the Light Lung cases, yields to a shift of about 2 mm of the rebuildup portion of the curve for the two algorithms. This difference could partly ascribed to the boundary handling from different algorithms (considering that no grid alignment is performed between image and dose grid voxels), or also to the variance reduction techniques implemented in VMC++ to decrease statistical noise.
The Light Lung DD curve has a noticeably steeper gradient that starts 24 cm distal to the interface. The horizontal profiles through the light lung insert enhance the display of this unexpected increase in dose a few cm from the field edge and the interface, an effect that is more pronounced at deeper distances. Inside the most internal light lung material the differences between Acuros XB and VMC++ are small. The calculations for very low densities prove to be critical for all algorithms since this density range enhanced the inaccuracies coming from different approximations, as e.g. the energy cutoff for electron interactions, present also in Monte Carlo simulations.
Acuros XB and VMC++ show good mutual agreement in the bone tissue, while AAA presents inferior accuracy for low energy. The small peaks, few mm before and after the bone insert, are more pronounced for Acuros XB calculations. In dose to water calculations, Acuros XB shows the start of the increase of the depth dose curve for dose to water ~5 mm before the bone interface, while VMC++ anticipates this to ~10 mm before it.
Results from phantom B present the same, but enhanced, patterns and characteristics as phantom A. To note is the inability of AAA to properly model the presence of thin inhomogeneities.
For phantom B settings, that present thin inhomogeneity layers, a plain improvement is shown with Acuros XB version 11, due to the improved alignment of structures and dose voxels. In addition it can be noticed that the dose computed with Acuros XB version 11 inside the Air material layer presents much better agreement with VMC++ calculations, due to the inclusion in the human tissues list of the air material, that was considered as lung composition in version 10.
Twodimensional analysis: Gamma evaluation
Gamma Agreement Index GAI
6X  15X  

LF  SF  LF  SF  
Dose to medium  
NormalLung  Acuros XB  99.9  99.6  100.0  100.0 
AAA  91.2  91.6  98.9  66.6  
LightLung  Acuros XB  85.6  90.1  81.5  85.5 
AAA  47.9  6.3  18.4  1.6  
Bone  Acuros XB  99.9  99.8  100.0  100.0 
AAA  62.2  41.8  100.0  100.0  
Dose to water  
NormalLung  Acuros XB  99.8  99.2  100.0  99.3 
AAA  97.1  95.8  98.0  48.2  
LightLung  Acuros XB  83.5  90.5  83.8  90.0 
AAA  34.8  6.1  12.2  1.6  
Bone  Acuros XB  89.0  75.8  90.5  72.7 
AAA  79.8  97.4  18.3  12.6  
Dose rescaled to water  
NormalLung  Acuros XB  99.9  98.7  99.9  99.3 
AAA  99.5  93.3  97.6  51.8  
LightLung  Acuros XB  81.0  88.6  78.6  85.6 
AAA  29.9  6.0  7.8  1.6  
Bone  Acuros XB  99.9  99.8  99.9  99.9 
AAA  100.0  100.0  100.0  100.0 
Summarising the results from phantom A: the GAI (3%, 3 mm criteria) for Acuros XB (version 10), dose to medium, are in average 100%, 86%, 100%, for Normal Lung, Light Lung and Bone cases respectively. The same figures are 87%, 19%, 76% for AAA calculations. Considering the dose rescaled to water, where the comparison with AAA comparison is more relevant, GAI results are: 99%, 83%, 100% for Acuros XB, and 86%, 11%, 100% for AAA.
Those data imply that for low density materials, more than the specific modality to compute dose, the critical variable is identified in the mass density of the medium itself, while the crucial point for bone tissue is more related to the elemental composition and the ability to consider it in calculations.
From phantom B results the dose inside the Air layer presents rather low gamma values for both AAA and Acuros XB version 10.
The results here presented are in good agreement with what has been published by Bush et al[8] comparing Acuros XB calculations with BEAMnrc/DOSXYZnrc Monte Carlo simulations. The key point from the two studies remains the high level of accuracy of Acuros XB implementation in Eclipse when simple heterogeneities in phantom are involved. Anyway, different settings have been used in the two studies, mainly in the two Monte Carlo algorithms.
In their work, Bush et al, used different elemental compositions and density ranges for HU to mass density conversion with respect to what is implemented in Acuros XB. This discrepancy is not used in the present paper, where the same Acuros XB chemical composition and density range are set for VMC++ calculations.
Also the electron energy cutoff is different for all calculations: 700 keV as kinetic+electron rest mass in Monte Carlo calculation from Bush et al; in VMC++ of the present study it is automatically selected and based upon the density of the material density; it is set to 500 keV (version 10) or 200 keV (version 11) as kinetic energy only for Acuros XB calculations.
Those two examples of differences point to unavoidable approximations of all dose calculations, including Monte Carlo. Those examples enforce the need of publishing different comparisons, presenting various characteristics, in order to give to the community the opportunity to read about results coming from different approaches.
Conclusions
The new Acuros XB photon dose calculation engine is tested for accuracy against Monte Carlo simulations in phantoms with simple geometrical heterogeneities in its clinical version 10. The comparison is extended also to the widely used AAA algorithm. Good agreement between Acuros XB and Monte Carlo is shown, even in extreme cases of materials of very low density and for low energy and small fields. Some differences between different algorithms are pointed out at interfaces between different materials. In those cases, Acuros XB and VMC++ present differences mainly in the rebuildup region. The agreement in this region improves with the newer version 11 of the Acuros XB algorithm.
In general, results suggest that the Acuros XB algorithm is mature for clinical implementation and can provide a valid and accurate alternative to Monte Carlo calculations.
Declarations
Acknowledgements
The authors thank the whole Varian Medical System group in Helsinki, Finland, especially Pekka Uusitalo, Tuomas Torsti, Laura Korhonen, Viljo Petaja and Stephen Thompson for the fruitful discussions arising during the evaluation and testing phase of the Acuros XB through its various developing versions.
Authors’ Affiliations
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