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Dive into the research topics where Damian Bernard is active.

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Featured researches published by Damian Bernard.


Medical Physics | 2004

Dose perturbation induced by radiographic contrast inside brachytherapy balloon applicators

Michael C. Kirk; Wen C. Hsi; James C.H. Chu; Honquan Niu; Z Hu; Damian Bernard; Adam Dickler; Cam Nguyen

Phantom measurements and Monte Carlo calculations have been performed for the purpose of characterizing the dose perturbation caused by radiographic contrast inside the MammoSite breast brachytherapy applicator. Specifically, the dose perturbation is quantified as a heterogeneity correction factor (HCF) for various balloon radii and contrast concentration levels. The dose perturbation is larger for larger balloon radii and higher contrast concentrations. Based on a validated Monte Carlo simulation, the calculated HCF values are 0.99 for a 2 cm radius balloon and 0.98 for a 3 cm radius balloon at 6% contrast concentration levels, and 0.89 and 0.87 for 2 and 3 cm radius balloons, respectively, at 100% contrast concentrations. For a typical implanted balloon radius of 2.4 cm, the HCF values decrease from 0.99 at 6% contrast concentration to 0.90 at 100% contrast concentration. For balloons implanted in patients at our institution, the mean HCF is 0.99, corresponding to a dose reduction of approximately 1%. The contrast effect results in a systematic reduction in the delivered dose, therefore the minimal amount of radiographic contrast necessary should be used.


Brachytherapy | 2008

A dosimetric comparison of Xoft Axxent Electronic Brachytherapy and iridium-192 high-dose-rate brachytherapy in the treatment of endometrial cancer

Adam Dickler; Michael C. Kirk; Alan B. Coon; Damian Bernard; T Zusag; Jacob Rotmensch; David E. Wazer

PURPOSE This analysis was undertaken to dosimetrically compare iridium-192 high-dose-rate brachytherapy (IB) and Xoft Axxent Electronic Brachytherapy (XB; Xoft Inc., Sunnyvale, CA) in the treatment of endometrial cancer. METHODS AND MATERIALS The planning CT scans from 11 patients previously treated with IB were used to construct hypothetical treatment plans using the source characteristics of the XB device. The mean V95, V100, and V150 (percent of the planning target volume that received 95%, 100%, and 150% of the prescription dose) were calculated. For both the bladder and rectum, the V35 (percent of the organ that received 35% of the prescription dose) and V50 (percent of the organ that received 50% of the prescription dose) were calculated for each patient using both methods of vaginal brachytherapy. RESULTS The mean %V95 was 99.7% vs. 99.6% (p = ns) and the mean %V100 was 99.0% vs. 99.1% (p = ns) for the IB and XB methods, respectively. The mean %V150 was 35.8% vs. 58.9% (p < 0.05) for the IB and XB methods, respectively. The mean bladder %V35 was 47.7% vs. 27.4% (p < 0.05) and the mean bladder %V50 was 26.5% vs. 15.9% (p < 0.05) for the IB and XB methods, respectively. The mean rectal %V35 was 48.3% vs. 28.3% (p < 0.05) and the mean rectal %V50 was 27.8% vs. 17.0% (p < 0.05) for the IB and XB methods, respectively. CONCLUSIONS The IB and XB methods of vaginal brachytherapy offer equivalent target volume coverage; however, the XB method allows increased sparing of the bladder and rectum.


Brachytherapy | 2009

A dosimetric comparison of MammoSite and ClearPath high-dose-rate breast brachytherapy devices

Adam Dickler; Neil Seif; Michael C. Kirk; Mita Patel; Damian Bernard; Alan B. Coon; Kambiz Dowlatshahi; Rupak K. Das; Rakesh R. Patel

PURPOSE A new form of partial breast irradiation (PBI), ClearPath (CP) breast brachytherapy, has been introduced. We present our results of a dosimetric comparison of MammoSite (MS) and CP PBI. METHODS AND MATERIALS The dimensions of the CP device were reconstructed onto the MS planning CT scans for 15 previously treated patients. The mean %V(100), %V(150), %V(200) (percent of the PTV that received 100%, 150%, and 200% of the prescription dose, respectively), ipsilateral breast %V(50) (percent of the ipsilateral normal breast that received 50% of the prescription dose), ipsilateral lung %V(30) (percent of the ipsilateral lung that received 30% of the prescription dose), the heart %V(5) (percent of the heart that received 5% of the prescription dose), and the maximum skin point dose per fraction were then determined for each patient using the two methods of balloon-based PBI. RESULTS The mean %V(100) was 96.5% vs. 96.5%, the mean %V(150) was 42.1% vs. 42.9% (p=ns), and the mean V(200) was 11.4% vs. 15.2% (p<.05) for the MS and CP methods, respectively. The mean ipsilateral breast %V(50) was 19.8% vs.18.0% (p<.05), the mean ipsilateral lung %V(30) was 3.7% vs. 2.8% (p<.05), the mean heart %V(5) was 57.0% vs. 54.3% (p<.05), and the maximum skin point dose per fraction was 312.2 and 273.6cGy (p<.05) for the MS and CP methods, respectively. CONCLUSIONS The MS and CP methods of PBI offer comparable target volume coverage; however, the CP device achieves increased normal tissue sparing.


Journal of Applied Clinical Medical Physics | 2004

Monte Carlo calculations of output factors for clinically shaped electron fields.

J Turian; B Smith; Damian Bernard; Katherine L. Griem; James C.H. Chu

We report on the use of the EGS4/BEAM Monte Carlo technique to predict the output factors for clinically relevant, irregularly shaped inserts as they intercept a linear accelerators electron beams. The output factor for a particular combination—energy, cone, insert, and source‐to‐surface distance (SSD)—is defined in accordance with AAPM TG‐25 as the product of cone correction factor and insert correction factor, evaluated at the depth of maximum dose. Since cone correction factors are easily obtained, we focus our investigation on the insert correction factors (ICFs). An analysis of the inserts used in routine clinical practice resulted in the identification of a set of seven “idealized” shapes characterized by specific parameters. The ICFs for these shapes were calculated using a Monte Carlo method (EGS4/BEAM) and measured for a subset of them using an ion chamber and well‐established measurement methods. Analytical models were developed to predict the Monte Carlo–calculated ICF values for various electron energies, cone sizes, shapes, and SSDs. The goodness‐of‐fit between predicted and Monte Carlo–calculated ICF values was tested using the Kolmogorov–Smirnoff statistical test. Results show that Monte Carlo–calculated ICFs match the measured values within 2.0% for most of the shapes considered, except for few highly elongated fields, where deviations up to 4.0% were recorded. Predicted values based on analytical modeling agree with measured ICF values within 2% to 3% for all configurations. We conclude that the predicted ICF values based on modeling of Monte Carlo–calculated values could be introduced in clinical use. PACS numbers: 87.53.Wz, 87.53.Hv


Journal of Applied Clinical Medical Physics | 2005

Performance of magnetic field guided navigation system for interventional neurosurgical and cardiac procedures

James C.H. Chu; Wen Chien Hsi; Lincoln Hubbard; Yunkai Zhang; Damian Bernard; Pamela Reeder; Demetrius K. Lopes

A hospital‐based magnetic guidance system (MGS) was installed to assist a physician in navigating catheters and guide wires during interventional cardiac and neurosurgical procedures. The objective of this study is to examine the performance of this magnetic field‐guided navigation system. Our results show that the systems radiological imaging components produce images with quality similar to that produced by other modern fluoroscopic devices. The systems magnetic navigation components also deflect the wire and catheter tips toward the intended direction. The physician, however, will have to oversteer the wire or catheter when defining the steering angle during the procedure. The MGS could be clinically useful in device navigation deflection and vessel access. PACS numbers: 07.55.Db, 07.85.‐m


Medical Dosimetry | 2011

HELICAL TOMOTHERAPY DELIVERY OF AN IMRT BOOST IN LIEU OF INTERSTITIAL BRACHYTHERAPY IN THE SETTING OF GYNECOLOGIC MALIGNANCY: FEASIBILITY AND DOSIMETRIC COMPARISON

Benjamin T. Gielda; Anand P. Shah; James C. Marsh; Joseph P. Smart; Damian Bernard; Jacob Rotmensch; Katherine L. Griem

Interstitial brachytherapy is an important means by which to improve local control in gynecologic malignancy when intracavitary brachytherapy is untenable. Patients unable to receive brachytherapy have traditionally received conventional external beam radiation alone with modest results. We investigated the ability of Tomotherapy (Tomotherapy Inc., Madison, WI) to replace interstitial brachytherapy. Six patients were selected. The planning CT of each patient was contoured with the planning target volume (PTV), bladder, rectum, femoral heads, and bowel. Identical contour sets were exported to Tomotherapy and Nucletron PLATO (Nucletron B.V., Veenendaal, The Netherlands). With Tomotherapy, the PTV was prescribed 31 Gy in 5 fractions to 90% of the volume. With PLATO, 600 cGy × 5 fractions was prescribed to the surface of the PTV. Dose delivered was normalized to 2 Gy fractions (EQD2) and added to a hypothetical homogenous 45-Gy pelvic dose. Tomotherapy achieved a D90 of 87 Gy EQD2 versus 86 Gy with brachytherapy. PTV dose was more homogeneous with tomotherapy. The dose to the most at-risk 2 mL of bladder and rectum with Tomotherapy was of 78 and 71 Gy EQD2 versus 81 and 75 Gy with brachytherapy. Tomotherapy delivered more dose to the femoral heads (mean 1.23 Gy per fraction) and bowel. Tomotherapy was capable of replicating the peripheral dose achieved with brachytherapy, without the PTV hotspots inherent to interstitial brachytherapy. Similar maximum doses to bowel and bladder were achieved with both methods. Excessive small bowel and femoral head toxicity may result if previous pelvic irradiation is not planned accordingly. Significant challenges related to interfraction and intrafraction motion must be overcome if treatment of this nature is to be contemplated.


International Journal of Radiation Oncology Biology Physics | 2003

Design optimization of intraoperative radiotherapy cones

Damian Bernard; James C.H. Chu; Martin Rozenfeld; Lawrence H. Lanzl; Antonio Pagnamenta; Amod Saxena

PURPOSE Electron intraoperative cones (EIORCs) commonly used for intraoperative radiation therapy (IORT) often generate high-dose regions at superficial depths. This study was performed to optimize the use of rings in the EIORC design that reduces the high-dose region while minimizing the loss of the treatment volume at the prescribed depth. METHODS AND MATERIALS Monte Carlo simulations were performed to study the dosimetry properties of various EIORC designs. Simulations were conducted with EIORCs of various internal radii, lengths, and material compositions irradiated by available electron beam energies. The data were analyzed in terms of volume receiving > 105% and < 90% of the prescription dose, respectively. RESULTS The high-dose volume increases with the EIORC size and the electron beam energy. The use of a ring inside the EIORC reduces the 105% dose volume but also increases the sub-90% volume. The degree of change of these volumes depends on the ring thickness and position. CONCLUSION The optimal ring position is about 10 cm from the bottom of the EIORC, regardless of the EIORC material, geometry, or electron energy. The optimal thickness of the ring is dependent on its material composition, the beam energy, and the preferred compromise between a uniform dose profile and a loss of treatment volume.


Journal of Applied Clinical Medical Physics | 2005

Limited accuracy of dose calculation for large fields at deep depths using the BrainSCAN v5.21 treatment-planning system

Wen C. Hsi; Yunkai Zhang; Michael C. Kirk; Damian Bernard; James C.H. Chu

The Varian 120 multileaf collimator (MLC) has a leaf thickness of 5 mm projected at the isocenter plane and can deliver a radiation beam of large field size (up to 30 cm) to be used in intensity‐modulated radiotherapy (IMRT). Often the dose must be delivered to depths greater than 20 cm. Therefore, during the commissioning of the BrainSCAN v5.21 or any radiation treatment‐planning (RTP) systems, extensive testing of dose and monitor unit calculations must encompass the field sizes (1 cm to 30 cm) and the prescription depths (1 cm to 20 cm). Accordingly, the central‐axis percent depth doses (PDDs) and off‐axis percentage profiles must be measured at several depths for various field sizes. The data for this study were acquired with a 6‐MV X‐ray beam from a Varian 2100EX LINAC with a water phantom at a source‐to‐surface distance (SSD) of 100 cm. These measurements were also used to generate a photon beam module, based on a photon pencil beam dose‐calculation algorithm with a fast‐Fourier transform method. To commission the photon beam module used in our BrainSCAN RTP system, we performed a quantitative comparison of measured and calculated central‐axis depth doses and off‐axis profiles. Utilizing the principles of dose difference and distance‐to‐agreement introduced by Van Dyk et al. [Commissioning and quality assurance of treatment planning computers. Int J Radiat Oncol Biol Phys. 1993; 26:261—273], agreements between calculated and measured doses are <2% and <2 mm for the regions of low‐ and high‐dose gradients, respectively. However, large errors (up to ~5% and ~7% for 20‐cm and 30‐cm fields, respectively, at the depth 20 cm) were observed for monitor unit calculations. For a given field size, the disagreement increased with the depth. Similarly, for a given depth the disagreement also increased with the field size. These large systematic errors were caused by using the tissue maximum ratio (TMR) in BrainSCAN v5.21 without considering increased field size as depth increased. These errors have been reported to BrainLAB. PACS number: 87.53.‐j


Journal of Applied Clinical Medical Physics | 2010

Comparison of tumor and normal tissue dose for accelerated partial breast irradiation using an electronic brachytherapy eBx source and an Iridium-192 source.

S Ahmad; D Johnson; Jessica R. Hiatt; D. Timothy Still; Eli E. Furhang; David Marsden; Frank Kearly; Damian Bernard; Randall W. Holt

The objective of this study has been to compare treatment plans for patients treated with electronic brachytherapy (eBx) using the Axxent System as adjuvant therapy for early stage breast cancer with treatment plans prepared from the same CT image sets using an Ir‐192 source. Patients were implanted with an appropriately sized Axxent balloon applicator based on tumor cavity size and shape. A CT image of the implanted balloon was utilized for developing both eBx and Ir‐192 brachytherapy treatment plans. The prescription dose was 3.4 Gy per fraction for 10 fractions to be delivered to 1 cm beyond the balloon surface. Iridium plans were provided by the sites on 35 of the 44 patients enrolled in the study. The planning target volume coverage was very similar when comparing sources for each patient as well as between patients. There were no statistical differences in mean %V100. The percent of the planning target volume in the high dose region was increased with eBx as compared with Iridium (p<0.001). The mean maximum calculated skin and rib doses did not vary greatly between eBx and Iridium. By contrast, the doses to the ipsilateral lung and the heart were significantly lower with eBx as compared with Iridium (p<0.0001). The total nominal dwell times required for treatment can be predicted by using a combination of the balloon fill volume and planned treatment volume (PTV). This dosimetric comparison of eBx and Iridium sources demonstrates that both forms of balloon‐based brachytherapy provide comparable dose to the planning target volume. Electronic brachytherapy is significantly associated with increased dose at the surface of the balloon and decreased dose outside the PTV, resulting in significantly increased tissue sparing in the heart and ipsilateral lung. PACS numbers: 87,53.Jw, 87.55.dk, 87.55.D‐,87.56 b‐,87.56.bg


Physics in Medicine and Biology | 2018

Characterization of Compton-scatter imaging with an analytical simulation method

Kevin C. Jones; Gage Redler; A Templeton; Damian Bernard; J Turian; James C.H. Chu

By collimating the photons scattered when a megavoltage therapy beam interacts with the patient, a Compton-scatter image may be formed without the delivery of an extra dose. To characterize and assess the potential of the technique, an analytical model for simulating scatter images was developed and validated against Monte Carlo (MC). For three phantoms, the scatter images collected during irradiation with a 6 MV flattening-filter-free therapy beam were simulated. Images, profiles, and spectra were compared for different phantoms and different irradiation angles. The proposed analytical method simulates accurate scatter images up to 1000 times faster than MC. Minor differences between MC and analytical simulated images are attributed to limitations in the isotropic superposition/convolution algorithm used to analytically model multiple-order scattering. For a detector placed at 90° relative to the treatment beam, the simulated scattered photon energy spectrum peaks at 140-220 keV, and 40-50% of the photons are the result of multiple scattering. The high energy photons originate at the beam entrance. Increasing the angle between source and detector increases the average energy of the collected photons and decreases the relative contribution of multiple scattered photons. Multiple scattered photons cause blurring in the image. For an ideal 5 mm diameter pinhole collimator placed 18.5 cm from the isocenter, 10 cGy of deposited dose (2 Hz imaging rate for 1200 MU min-1 treatment delivery) is expected to generate an average 1000 photons per mm2 at the detector. For the considered lung tumor CT phantom, the contrast is high enough to clearly identify the lung tumor in the scatter image. Increasing the treatment beam size perpendicular to the detector plane decreases the contrast, although the scatter subject contrast is expected to be greater than the megavoltage transmission image contrast. With the analytical method, real-time tumor tracking may be possible through comparison of simulated and acquired patient images.

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James C.H. Chu

Rush University Medical Center

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Michael C. Kirk

Rush University Medical Center

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Alan B. Coon

Rush University Medical Center

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Adam Dickler

Rush University Medical Center

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J Turian

Rush University Medical Center

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Katherine L. Griem

Rush University Medical Center

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A Templeton

Rush University Medical Center

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Gage Redler

Rush University Medical Center

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R Yao

Rush University Medical Center

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J Chu

Rush University Medical Center

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