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Dive into the research topics where Åsa Carlsson Tedgren is active.

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Featured researches published by Åsa Carlsson Tedgren.


Medical Physics | 2012

Report of the Task Group 186 on model-based dose calculation methods in brachytherapy beyond the TG-43 formalism: Current status and recommendations for clinical implementation

Luc Beaulieu; Åsa Carlsson Tedgren; Jean-François Carrier; S Davis; Firas Mourtada; Mark J. Rivard; Rowan M. Thomson; F Verhaegen; Todd A. Wareing; Jeffrey F. Williamson

The charge of Task Group 186 (TG-186) is to provide guidance for early adopters of model-based dose calculation algorithms (MBDCAs) for brachytherapy (BT) dose calculations to ensure practice uniformity. Contrary to external beam radiotherapy, heterogeneity correction algorithms have only recently been made available to the BT community. Yet, BT dose calculation accuracy is highly dependent on scatter conditions and photoelectric effect cross-sections relative to water. In specific situations, differences between the current water-based BT dose calculation formalism (TG-43) and MBDCAs can lead to differences in calculated doses exceeding a factor of 10. MBDCAs raise three major issues that are not addressed by current guidance documents: (1) MBDCA calculated doses are sensitive to the dose specification medium, resulting in energy-dependent differences between dose calculated to water in a homogeneous water geometry (TG-43), dose calculated to the local medium in the heterogeneous medium, and the intermediate scenario of dose calculated to a small volume of water in the heterogeneous medium. (2) MBDCA doses are sensitive to voxel-by-voxel interaction cross sections. Neither conventional single-energy CT nor ICRU∕ICRP tissue composition compilations provide useful guidance for the task of assigning interaction cross sections to each voxel. (3) Since each patient-source-applicator combination is unique, having reference data for each possible combination to benchmark MBDCAs is an impractical strategy. Hence, a new commissioning process is required. TG-186 addresses in detail the above issues through the literature review and provides explicit recommendations based on the current state of knowledge. TG-43-based dose prescription and dose calculation remain in effect, with MBDCA dose reporting performed in parallel when available. In using MBDCAs, it is recommended that the radiation transport should be performed in the heterogeneous medium and, at minimum, the dose to the local medium be reported along with the TG-43 calculated doses. Assignments of voxel-by-voxel cross sections represent a particular challenge. Electron density information is readily extracted from CT imaging, but cannot be used to distinguish between different materials having the same density. Therefore, a recommendation is made to use a number of standardized materials to maintain uniformity across institutions. Sensitivity analysis shows that this recommendation offers increased accuracy over TG-43. MBDCA commissioning will share commonalities with current TG-43-based systems, but in addition there will be algorithm-specific tasks. Two levels of commissioning are recommended: reproducing TG-43 dose parameters and testing the advanced capabilities of MBDCAs. For validation of heterogeneity and scatter conditions, MBDCAs should mimic the 3D dose distributions from reference virtual geometries. Potential changes in BT dose prescriptions and MBDCA limitations are discussed. When data required for full MBDCA implementation are insufficient, interim recommendations are made and potential areas of research are identified. Application of TG-186 guidance should retain practice uniformity in transitioning from the TG-43 to the MBDCA approach.


Medical Physics | 2008

Optimization of the computational efficiency of a 3D, collapsed cone dose calculation algorithm for brachytherapy

Åsa Carlsson Tedgren; Anders Ahnesjö

Brachytherapy dose calculations based on point kernel superposition using the collapsed cone method have been shown to accurately model the influence from finite dimensions of the patient and effects from heterogeneities including those of high atomic numbers. The collapsed cone method is for brachytherapy applications most effectively implemented through a successive-scattering approach, in which the dose from once and higher order of scattered photons is calculated separately and in successive scatter order. The calculation speed achievable is directly proportional to the number of directions used for point kernel discretization and to the number of voxels in the volume. In this work we investigate how to best divide the total number of directions between the two steps of successive-scattering dose calculations. Results show that the largest fraction of the total number of directions should be utilized in calculating the first-scatter dose. Also shown is how the number of directions required for keeping discretization artifacts at acceptably low levels decreases significantly in multiple-source configurations, as a result of the dose gradients being less steep than those around single sources. Investigating the number of kernel directions required to keep artifacts low enough within the high dose region of an implant (i.e., for dose levels above approximately 5%-10% of the mean central target dose) reveals similar figures for brachytherapy as for external beam applications, where collapsed cone superposition is clinically used. Also shown is that approximating point kernels with their isotropic average leads to small dose differences at low and intermediate energies, implying that the collapsed cone calculations can be done in a single operation common to all sources of the implant at these energies. The current findings show that collapsed cone calculations can be achieved for brachytherapy with the same efficiency as for external beams. This, combined with recent results on gains in efficiency through implementing the algorithm on graphical card parallel hardware indicates that dose can be calculated with account for heterogeneities and finite dimensions within a few seconds for large voxel arrays and is therefore of interest for practical application to treatment planning.


Medical Physics | 2015

A generic high‐dose rate 192Ir brachytherapy source for evaluation of model‐based dose calculations beyond the TG‐43 formalism

Facundo Ballester; Åsa Carlsson Tedgren; Domingo Granero; Annette Haworth; Firas Mourtada; Gabriel P. Fonseca; K. Zourari; P. Papagiannis; Mark J. Rivard; Frank-André Siebert; Ron S. Sloboda; Ryan L. Smith; Rowan M. Thomson; F Verhaegen; J. Vijande; Yunzhi Ma; Luc Beaulieu

PURPOSE In order to facilitate a smooth transition for brachytherapy dose calculations from the American Association of Physicists in Medicine (AAPM) Task Group No. 43 (TG-43) formalism to model-based dose calculation algorithms (MBDCAs), treatment planning systems (TPSs) using a MBDCA require a set of well-defined test case plans characterized by Monte Carlo (MC) methods. This also permits direct dose comparison to TG-43 reference data. Such test case plans should be made available for use in the software commissioning process performed by clinical end users. To this end, a hypothetical, generic high-dose rate (HDR) (192)Ir source and a virtual water phantom were designed, which can be imported into a TPS. METHODS A hypothetical, generic HDR (192)Ir source was designed based on commercially available sources as well as a virtual, cubic water phantom that can be imported into any TPS in DICOM format. The dose distribution of the generic (192)Ir source when placed at the center of the cubic phantom, and away from the center under altered scatter conditions, was evaluated using two commercial MBDCAs [Oncentra(®) Brachy with advanced collapsed-cone engine (ACE) and BrachyVision ACUROS™ ]. Dose comparisons were performed using state-of-the-art MC codes for radiation transport, including ALGEBRA, BrachyDose, GEANT4, MCNP5, MCNP6, and PENELOPE2008. The methodologies adhered to recommendations in the AAPM TG-229 report on high-energy brachytherapy source dosimetry. TG-43 dosimetry parameters, an along-away dose-rate table, and primary and scatter separated (PSS) data were obtained. The virtual water phantom of (201)(3) voxels (1 mm sides) was used to evaluate the calculated dose distributions. Two test case plans involving a single position of the generic HDR (192)Ir source in this phantom were prepared: (i) source centered in the phantom and (ii) source displaced 7 cm laterally from the center. Datasets were independently produced by different investigators. MC results were then compared against dose calculated using TG-43 and MBDCA methods. RESULTS TG-43 and PSS datasets were generated for the generic source, the PSS data for use with the ace algorithm. The dose-rate constant values obtained from seven MC simulations, performed independently using different codes, were in excellent agreement, yielding an average of 1.1109 ± 0.0004 cGy/(h U) (k = 1, Type A uncertainty). MC calculated dose-rate distributions for the two plans were also found to be in excellent agreement, with differences within type A uncertainties. Differences between commercial MBDCA and MC results were test, position, and calculation parameter dependent. On average, however, these differences were within 1% for ACUROS and 2% for ace at clinically relevant distances. CONCLUSIONS A hypothetical, generic HDR (192)Ir source was designed and implemented in two commercially available TPSs employing different MBDCAs. Reference dose distributions for this source were benchmarked and used for the evaluation of MBDCA calculations employing a virtual, cubic water phantom in the form of a CT DICOM image series. The implementation of a generic source of identical design in all TPSs using MBDCAs is an important step toward supporting univocal commissioning procedures and direct comparisons between TPSs.


Medical Physics | 2011

Response of LiF:Mg,Ti thermoluminescent dosimeters at photon energies relevant to the dosimetry of brachytherapy (<1 MeV)

Åsa Carlsson Tedgren; Angelica Hedman; Jan-Erik Grindborg; Gudrun Alm Carlsson

PURPOSE High energy photon beams are used in calibrating dosimeters for use in brachytherapy since absorbed dose to water can be determined accurately and with traceability to primary standards in such beams, using calibrated ion chambers and standard dosimetry protocols. For use in brachytherapy, beam quality correction factors are needed, which include corrections for differences in mass energy absorption properties between water and detector as well as variations in detector response (intrinsic efficiency) with radiation quality, caused by variations in the density of ionization (linear energy transfer (LET) -distributions) along the secondary electron tracks. The aim of this work was to investigate experimentally the detector response of LiF:Mg,Ti thermoluminescent dosimeters (TLD) for photon energies below 1 MeV relative to (60)Co and to address discrepancies between the results found in recent publications of detector response. METHODS LiF:Mg,Ti dosimeters of formulation MTS-N Poland were irradiated to known values of air kerma free-in-air in x-ray beams at tube voltages 25-250 kV, in (137)Cs- and (60)Co-beams at the Swedish Secondary Standards Dosimetry Laboratory. Conversions from air kerma free-in-air into values of mean absorbed dose in the dosimeters in the actual irradiation geometries were made using EGSnrc Monte Carlo simulations. X-ray energy spectra were measured or calculated for the actual beams. Detector response relative to that for (60)Co was determined at each beam quality. RESULTS An increase in relative response was seen for all beam qualities ranging from 8% at tube voltage 25 kV (effective energy 13 keV) to 3%-4% at 250 kV (122 keV effective energy) and (137)Cs with a minimum at 80 keV effective energy (tube voltage 180 kV). The variation with effective energy was similar to that reported by Davis et al. [Radiat. Prot. Dosim. 106, 33-43 (2003)] with our values being systematically lower by 2%-4%. Compared to the results by Nunn et al. [Med. Phys. 35, 1861-1869 (2008)], the relative detector response as a function of effective energy differed in both shape and magnitude. This could be explained by the higher maximum read-out temperature (350 °C) used by Nunn et al. [Med. Phys. 35, 1861-1869 (2008)], allowing light emitted from high-temperature peaks with a strong LET dependence to be registered. Use of TLD-100 by Davis et al. [Radiat. Prot. Dosim. 106, 33-43 (2003)] with a stronger super-linear dose response compared to MTS-N was identified as causing the lower relative detector response in this work. CONCLUSIONS Both careful dosimetry and strict protocols for handling the TLDs are required to reach solid experimental data on relative detector response. This work confirms older findings that an over-response relative to (60)Co exists for photon energies below 200-300 keV. Comparison with the results from the literature indicates that using similar protocols for annealing and read-out, dosimeters of different makes (TLD-100, MTS-N) differ in relative detector response. Though universality of the results has not been proven and further investigation is needed, it is anticipated that with the use of strict protocols for annealing and read-out, it will be possible to determine correction factors that can be used to reduce uncertainties in dose measurements around brachytherapy sources at photon energies where primary standards for absorbed dose to water are not available.


Medical Physics | 2010

Response of lithium formate EPR dosimeters at photon energies relevant to the dosimetry of brachytherapy

Emelie Adolfsson; Gudrun Alm Carlsson; Jan-Erik Grindborg; Håkan Gustafsson; Eva Lund; Åsa Carlsson Tedgren

PURPOSE To investigate experimentally the energy dependence of the detector response of lithium formate EPR dosimeters for photon energies below 1 MeV relative to that atC60o energies. High energy photon beams are used in calibrating dosimeters for use in brachytherapy since the absorbed dose to water can be determined with high accuracy in such beams using calibrated ion chambers and standard dosimetry protocols. In addition to any differences in mass-energy absorption properties between water and detector, variations in radiation yield (detector response) with radiation quality, caused by differences in the density of ionization in the energy imparted (LET), may exist. Knowledge of an eventual deviation in detector response with photon energy is important for attaining high accuracy in measured brachytherapy dose distributions. METHODS Lithium formate EPR dosimeters were irradiated to known levels of air kerma in 25-250 kV x-ray beams and inC137s and C60o beams at the Swedish Secondary Standards Dosimetry Laboratory. Conversions from air kerma free in air into values of mean absorbed dose to the detectors were made using EGSnrc MC simulations and x-ray energy spectra measured or calculated for the actual beams. The signals from the detectors were measured using EPR spectrometry. Detector response (the EPR signal per mean absorbed dose to the detector) relative to that for C60o was determined for each beam quality. RESULTS Significant decreases in the relative response ranging from 5% to 6% were seen for x-ray beams at tube voltages≤180kV. No significant reduction in the relative response was seen for C137s and 250 kV x rays. CONCLUSIONS When calibrated inC60o or MV photon beams, corrections for the photon energy dependence of detector response are needed to achieve the highest accuracy when using lithium formate EPR dosimeters for measuring absorbed doses around brachytherapy sources emitting photons in the energy range of 20-150 keV such as Y169b and electronic sources.


Medical Physics | 2012

Impact of Using Linear Optimization Models in Dose Planning for HDR Brachytherapy

Åsa Holm; Torbjörn Larsson; Åsa Carlsson Tedgren

PURPOSE Dose plans generated with optimization models hitherto used in high-dose-rate (HDR) brachytherapy have shown a tendency to yield longer dwell times than manually optimized plans. Concern has been raised for the corresponding undesired hot spots, and various methods to mitigate these have been developed. The hypotheses upon this work is based are (a) that one cause for the long dwell times is the use of objective functions comprising simple linear penalties and (b) that alternative penalties, as these are piecewise linear, would lead to reduced length of individual dwell times. METHODS The characteristics of the linear penalties and the piecewise linear penalties are analyzed mathematically. Experimental comparisons between the two types of penalties are carried out retrospectively for a set of prostate cancer patients. RESULTS When the two types of penalties are compared, significant changes can be seen in the dwell times, while most dose-volume parameters do not differ significantly. On average, total dwell times were reduced by 4.2%, with a reduction of maximum dwell times by 25%, when the alternative penalties were used. CONCLUSIONS The use of linear penalties in optimization models for HDR brachytherapy is one cause for the undesired long dwell times that arise in mathematically optimized plans. By introducing alternative penalties, a significant reduction in dwell times can be achieved for HDR brachytherapy dose plans. Although various measures for mitigating the long dwell times are already available, the observation that linear penalties contribute to their appearance is of fundamental interest.


Medical Physics | 2010

Characterization of a Co-60 unit at a secondary standard dosimetry laboratory: Monte Carlo simulations compared to measurements and results from the literature

Åsa Carlsson Tedgren; Sandro de Luelmo; Jan-Erik Grindborg

PURPOSE To compare a Monte Carlo (MC) characterization of a C60o unit at the Swedish Secondary Standard Dosimetry Laboratory (SSDL) with the results of both measurements and literature with the aims of (1) resolving a change in the ratio of air-kerma free in air Kair and absorbed dose to water Dw in a water phantom noted experimentally after a source exchange in the laboratory and (2) reviewing results from the literature on similar MC simulations. Although their use in radiotherapy is decreasing, the characteristics of C60o beams are of interest since C60o beams are utilized in calibrating ionization chambers for the absolute dosimetry of radiotherapy beams and as reference radiation quality in evaluating the energy dependence of radiation detectors and in studies on radiobiological effectiveness. METHODS The BEAMnrc MC code was used with a detailed geometrical model of the treatment head and two models of the C60o source representing the sources used before and after source exchange, respectively. The active diameters of the C60o sources were 1.5 cm in pellet form and 2.0 cm in sintered form. Measurements were performed on the actual unit at the Swedish SSDL. RESULTS Agreement was obtained between the MC and the measured results within the estimated uncertainties for beam profiles, water depth-dose curve, relative air-kerma output factors, and for the ratios of Kair/Dw before and after source exchange. The on-axis energy distribution of the photon fluence free in air for the unit loaded with its present (1.5 cm in diameter) source agreed closely with the results from the literature in which a source of the same make and active diameter, inside a different treatment head, was simulated. The spectrum for the larger (2.0 cm in diameter) source was in close agreement with another published spectrum, also modeling a C60o source with an active diameter of 2.0 cm inside a different treatment head. CONCLUSIONS The reduction in the value of Kair/Dw following source exchange was explained by the spectral differences between the two sources that were larger in the free in-air geometry used for Kair calibrations than at 5g/cm2 depth in the water phantom used for Dw calibrations. Literature review revealed differences between published in-air C60o spectra derived for sources of different active diameters, and investigators in need of an accurately determined C60o in-air spectrum should be aware of differences due to source active diameter.


Radiotherapy and Oncology | 2008

Audit on source strength determination for HDR and PDR 192Ir brachytherapy in Sweden

Åsa Carlsson Tedgren; Jan-Erik Grindborg

BACKGROUND AND PURPOSE To investigate the status of source strength determination in terms of reference air kerma rate (RAKR) for HDR and PDR (192)Ir brachytherapy in Sweden. MATERIALS AND METHODS RAKR was determined in each of the 14 Swedish afterloaders, using calibrated equipment from the Swedish Secondary Standard Dosimetry Laboratory. RESULTS Values of RAKR from the external audit, the hospitals and vendors agreed within the uncertainty limits guaranteed by the vendors. CONCLUSIONS The accuracy in RAKR determination has increased over the last years as a result of increased availability of interpolation standards for HDR (192)Ir and the increased use of robust well-type ion chambers designed for brachytherapy. It is recommended to establish a ratio between the RAKR value from own measurements at the hospital and that of the vendor since such a ratio embeds constant systematic differences due to e.g. varying traceability and therefore has the potential of being less uncertain than the RAKR alone. Traceability to primary standards for HDR (192)Ir sources will in the future significantly decrease the uncertainty in RAKR of (192)Ir brachytherapy.


Physics in Medicine and Biology | 2015

The collapsed cone algorithm for 192 Ir dosimetry using phantom-size adaptive multiple-scatter point kernels

Åsa Carlsson Tedgren; Mathieu Plamondon; Luc Beaulieu

The aim of this work was to investigate how dose distributions calculated with the collapsed cone (CC) algorithm depend on the size of the water phantom used in deriving the point kernel for multiple scatter. A research version of the CC algorithm equipped with a set of selectable point kernels for multiple-scatter dose that had initially been derived in water phantoms of various dimensions was used. The new point kernels were generated using EGSnrc in spherical water phantoms of radii 5 cm, 7.5 cm, 10 cm, 15 cm, 20 cm, 30 cm and 50 cm. Dose distributions derived with CC in water phantoms of different dimensions and in a CT-based clinical breast geometry were compared to Monte Carlo (MC) simulations using the Geant4-based brachytherapy specific MC code Algebra. Agreement with MC within 1% was obtained when the dimensions of the phantom used to derive the multiple-scatter kernel were similar to those of the calculation phantom. Doses are overestimated at phantom edges when kernels are derived in larger phantoms and underestimated when derived in smaller phantoms (by around 2% to 7% depending on distance from source and phantom dimensions). CC agrees well with MC in the high dose region of a breast implant and is superior to TG43 in determining skin doses for all multiple-scatter point kernel sizes. Increased agreement between CC and MC is achieved when the point kernel is comparable to breast dimensions. The investigated approximation in multiple scatter dose depends on the choice of point kernel in relation to phantom size and yields a significant fraction of the total dose only at distances of several centimeters from a source/implant which correspond to volumes of low doses. The current implementation of the CC algorithm utilizes a point kernel derived in a comparatively large (radius 20 cm) water phantom. A fixed point kernel leads to predictable behaviour of the algorithm with the worst case being a source/implant located well within a patient/phantom for which low doses at phantom edges can be overestimated by 2-5 %. It would be possible to improve the situation by using a point kernel for multiple-scatter dose adapted to the patient/phantom dimensions at hand.


Medical Physics | 2017

A generic TG-186 shielded applicator for commissioning model-based dose calculation algorithms for high-dose-rate 192Ir brachytherapy

Yunzhi Ma; J. Vijande; Facundo Ballester; Åsa Carlsson Tedgren; Domingo Granero; Annette Haworth; Firas Mourtada; Gabriel P. Fonseca; K. Zourari; P. Papagiannis; Mark J. Rivard; Frank−André Siebert; Ron S. Sloboda; Ryan L. Smith; Marc Chamberland; Rowan M. Thomson; Frank Verhaegen; Luc Beaulieu

Purpose: A joint working group was created by the American Association of Physicists in Medicine (AAPM), the European Society for Radiotherapy and Oncology (ESTRO), and the Australasian Brachytherapy Group (ABG) with the charge, among others, to develop a set of well‐defined test case plans and perform calculations and comparisons with model‐based dose calculation algorithms (MBDCAs). Its main goal is to facilitate a smooth transition from the AAPM Task Group No. 43 (TG‐43) dose calculation formalism, widely being used in clinical practice for brachytherapy, to the one proposed by Task Group No. 186 (TG‐186) for MBDCAs. To do so, in this work a hypothetical, generic high‐dose rate (HDR) 192Ir shielded applicator has been designed and benchmarked. Methods: A generic HDR 192Ir shielded applicator was designed based on three commercially available gynecological applicators as well as a virtual cubic water phantom that can be imported into any DICOM‐RT compatible treatment planning system (TPS). The absorbed dose distribution around the applicator with the TG‐186 192Ir source located at one dwell position at its center was computed using two commercial TPSs incorporating MBDCAs (Oncentra® Brachy with Advanced Collapsed‐cone Engine, ACE™, and BrachyVision ACUROS™) and state‐of‐the‐art Monte Carlo (MC) codes, including ALGEBRA, BrachyDose, egs_brachy, Geant4, MCNP6, and Penelope2008. TPS‐based volumetric dose distributions for the previously reported “source centered in water” and “source displaced” test cases, and the new “source centered in applicator” test case, were analyzed here using the MCNP6 dose distribution as a reference. Volumetric dose comparisons of TPS results against results for the other MC codes were also performed. Distributions of local and global dose difference ratios are reported. Results: The local dose differences among MC codes are comparable to the statistical uncertainties of the reference datasets for the “source centered in water” and “source displaced” test cases and for the clinically relevant part of the unshielded volume in the “source centered in applicator” case. Larger local differences appear in the shielded volume or at large distances. Considering clinically relevant regions, global dose differences are smaller than the local ones. The most disadvantageous case for the MBDCAs is the one including the shielded applicator. In this case, ACUROS agrees with MC within [−4.2%, +4.2%] for the majority of voxels (95%) while presenting dose differences within [−0.12%, +0.12%] of the dose at a clinically relevant reference point. For ACE, 95% of the total volume presents differences with respect to MC in the range [−1.7%, +0.4%] of the dose at the reference point. Conclusions: The combination of the generic source and generic shielded applicator, together with the previously developed test cases and reference datasets (available in the Brachytherapy Source Registry), lay a solid foundation in supporting uniform commissioning procedures and direct comparisons among treatment planning systems for HDR 192Ir brachytherapy.

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Eva Lund

Linköping University

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Josef Nilsson

Karolinska University Hospital

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Åsa Holm

Linköping University

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Firas Mourtada

Christiana Care Health System

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