Try a new search

Format these results:

Searched for:

in-biosketch:yes

person:chent08

Total Results:

70


Meshless Deformable Models for 3D Cardiac Motion and Strain Analysis from Tagged MRI

Wang, Xiaoxu; Chen, Ting; Zhang, Shaoting; Schaerer, Joel; Qian, Zhen; Huh, Suejung; Metaxas, Dimitris; Axel, Leon
Tagged Meganetic Resonance Image (TMRI) provides a direct and noninvasive way to visualize the in-wall deformation of the myocardium. Due to the through-plane motion, the tracking of 3D trajectories of the material points and the computation of 3D strain field call for the nessicity of building 3D cardiac deformable models. The intersections of three stacks of orthogonal tagging planes are material points in the myocardium. With these intersections as control points, 3D motion can be reconstructed with a novel meshless deformable model. Volumetric meshless deformable models describe an object as point cloud inside the object boundary and the coordinate of each point can be written in parametric functions. A generic heart mesh is registered on the tagged MRI with polar decomposition. A 3D meshless deformable model is generated and deformed with MR image tagging lines. Volumetric meshless deformable models are deformed by calculating the dynamics function and minimizing the local Laplacian coordinates. The similarity transformation of each point is computed by assuming its neighboring points are making the same transformation. The deformation is computed iteratively until the control points match the target positions in the consecutive image frame. The 3D strain field is computed from the 3D displacement field with Moving Least Squares (MLS). We demonstrate that meshless deformable models outperformed the finite element method (FEM) and the spline method with a numerical phantom. Meshless deformable models can track the trajectory of any material point in the myocardium and compute the 3D strain field of any particular area. The experimental results on in vivo healthy and patient heart MRI show that the meshless deformable model can fully recover the myocardium motion in three dimension.
PMCID:4876045
PMID: 25157446
ISSN: 0730-725x
CID: 1162302

The Role of Fibronectin on Spatial Organization in 3D Culture: a Model for Wound Healing after Breast Reconstruction and Post-Mastectomy Radiation Therapy [Meeting Abstract]

Hsia, Henry C; Tian, Sibo; Goyal, Sharad; Haffty, Bruce G; Chen, Ting; Foty, Ramsey A
ORIGINAL:0012465
ISSN: 1529-4242
CID: 2932392

Tagged MRI based cardiac motion modeling and toxicity evaluation in breast cancer radiotherapy

Chen, Ting; Reyhan, Meral; Yue, Ning; Metaxas, Dimitris N; Haffty, Bruce G; Goyal, Sharad
PMCID:4315014
PMID: 25692095
ISSN: 2234-943x
CID: 2932012

The Role of Fibronectin on Spatial Organization in 3D Culture: A Model for Wound Healing After Radiation Therapy [Meeting Abstract]

Tian, S.; Goyal, S.; Haffty, B. G.; Chen, T.; Hsia, H. C.
ISI:000342331403035
ISSN: 0360-3016
CID: 2932312

Frequency filtering based analysis on the cardiac induced lung tumor motion and its impact on the radiotherapy management

Chen, Ting; Qin, Songbing; Xu, Xiaoting; Jabbour, Salma K; Haffty, Bruce G; Yue, Ning J
PURPOSE/OBJECTIVES/OBJECTIVE:Lung tumor motion may be impacted by heartbeat in addition to respiration. This study seeks to quantitatively analyze heart-motion-induced tumor motion and to evaluate its impact on lung cancer radiotherapy. METHODS/MATERIALS/METHODS:Fluoroscopy images were acquired for 30 lung cancer patients. Tumor, diaphragm, and heart were delineated on selected fluoroscopy frames, and their motion was tracked and converted into temporal signals based on deformable registration propagation. The clinical relevance of heart impact was evaluated using the dose volumetric histogram of the redefined target volumes. RESULTS:Correlation was found between tumor and cardiac motion for 23 patients. The heart-induced motion amplitude ranged from 0.2 to 2.6 mm. The ratio between heart-induced tumor motion and the tumor motion was inversely proportional to the amplitude of overall tumor motion. When the heart motion impact was integrated, there was an average 9% increase in internal target volumes for 17 patients. Dose coverage decrease was observed on redefined planning target volume in simulated SBRT plans. CONCLUSIONS:The tumor motion of thoracic cancer patients is influenced by both heart and respiratory motion. The cardiac impact is relatively more significant for tumor with less motion, which may lead to clinically significant uncertainty in radiotherapy for some patients.
PMID: 25236714
ISSN: 1879-0887
CID: 2932042

Angular dependence of the MOSFET dosimeter and its impact on in vivo surface dose measurement in breast cancer treatment

Qin, S; Chen, T; Wang, L; Tu, Y; Yue, N; Zhou, J
The focus of this study is the angular dependence of two types of Metal Oxide Semiconductor Field Effect Transistor (MOSFET) dosimeters (MOSFET20 and OneDose/OneDosePlus) when used for surface dose measurements. External beam radiationat different gantry angles were delivered to a cubic solid water phantom with a MOSFET placed on the top surface at CAX. The long axis of the MOSFET was oriented along the gantry axis of rotation, with the dosimeter (bubble side) facing the radiation source. MOSFET-measured surface doses were compared against calibrated radiochromic film readings. It was found that both types of MOSFET dosimeters exhibited larger than previously reported angular dependence when measuring surface dose in beams at large oblique angles. For the MOSFET20 dosimeter the measured surface dose deviation against film readings was as high as 17% when the incident angle was 72 degrees to the norm of the phantom surface. It is concluded that some MOSFET dosimeters may have a strong angular dependence when placed on the surface of water-equivalent material, even though they may have an isotropic angular response when surrounded by uniform medium. Extra on-surface calibration maybe necessary before using MOSFET dosimeters for skin dose measurement in tangential fields.
PMID: 24206205
ISSN: 1533-0338
CID: 2932172

Parameterization of brachytherapy source phase space file for Monte Carlo-based clinical brachytherapy dose calculation

Zhang, M; Zou, W; Chen, T; Kim, L; Khan, A; Haffty, B; Yue, N J
A common approach to implementing the Monte Carlo method for the calculation of brachytherapy radiation dose deposition is to use a phase space file containing information on particles emitted from a brachytherapy source. However, the loading of the phase space file during the dose calculation consumes a large amount of computer random access memory, imposing a higher requirement for computer hardware. In this study, we propose a method to parameterize the information (e.g., particle location, direction and energy) stored in the phase space file by using several probability distributions. This method was implemented for dose calculations of a commercial Ir-192 high dose rate source. Dose calculation accuracy of the parameterized source was compared to the results observed using the full phase space file in a simple water phantom and in a clinical breast cancer case. The results showed the parameterized source at a size of 200 kB was as accurate as the phase space file represented source of 1.1 GB. By using the parameterized source representation, a compact Monte Carlo job can be designed, which allows an easy setup for parallel computing in brachytherapy planning.
PMID: 24374831
ISSN: 1361-6560
CID: 2932152

[Real patient data based cross verification of kilovoltage and megavoltage CT calibration for proton therapy]

Chen, T; et al
ORIGINAL:0012461
ISSN: 1345-5354
CID: 2932342

Optimization of heart block in the left-sided whole breast radiation treatments

Yue, Ning J; Goyal, Sharad; Park, Joo Han; Jones, Sheri; Xu, Xiaoting; Khan, Atif; Haffty, Bruce G; Chen, Ting
PURPOSE/OBJECTIVE:Blocks have been used to protect heart from potential radiation damage in left-sided breast treatments. Since cardiac motion pattern may not be fully captured on conventional 3DCT or 4DCT simulation scans, this study was intended to investigate the optimization of the heart block design taking the cardiac motion into consideration. MATERIALS AND METHODS/METHODS:Whole breast treatment plans using two opposed tangential fields were designed based on 4DCT simulation images for 10 left-sided breast cancer patients. Using an OBI system equipped to a Varian Linac, beam-eye viewed fluoroscopy images were acquired for each of the treatment beams after patient treatment setup, and the MLC heart blocks were overlaid onto the fluoroscopy images with an in-house software package. A non-rigid image registration and tracking algorithm was utilized to track the cardiac motion on the fluoroscopy images with minimal manual delineation for initialization, and the tracked cardiac motion information was used to optimize the heart block design to minimize the radiation damage to heart while avoiding the over-shielding that may lead to underdosing certain breast tissues. RESULTS:Twenty-three sets of fluoroscopy images were acquired on 23 different days of treatment for the 10 patients. As expected, heart moved under the influences of both respiratory and cardiac motion. It was observed that for 16 out of the 23 treatments, heart moved beyond the planed heart block into treatment fields and MLC had to be adjusted to fully block heart. The adjustment was made for all but one patient. The number of the adjusted MLC leaves ranged from 1 to 16 (mean = 10), and the MLC leaf position adjustment ranged from 2 to 10 mm (mean = 6 mm). The added heart block areas ranged from 3 to 1230 mm(2) (mean = 331 mm(2)). CONCLUSION/CONCLUSIONS:In left-sided whole breast radiation treatments, simulation CT (and 4DCT) based heart block design may not provide adequate heart protection for all the treatments. A fluoroscopy-based method has been developed to adaptively optimize the heart MLC block to achieve optimal heart protection.
PMCID:4251287
PMID: 25520942
ISSN: 2234-943x
CID: 2932092

Radiation oncology and medical devices (Part 2)

Yue, Ning J; Chen, Ting; Zou, Wei; et al
ORIGINAL:0012463
ISSN: 1674-1633
CID: 2932362