arXiv subjects

Ken Kang-Hsin Wang

Publications and source records attributed to Ken Kang-Hsin Wang.

8 recordsLinked to original sources

arXiv2026

Explicit pixel-value correction of lateral response artifacts in radiochromic film dosimetry: Evaluation of single-, double-, and triple-channel methods

Background:Flatbed scanners introduce a lateral response artifact (LRA) perpendicular to lamp motion. Because LRA varies with position, pixel value (PV), color channel, and film model, it may violate the channel-common perturbation assumption of multichannel dosimetry. Purpose:To characterize PV-domain LRA in EBT4 and EBT-XD films, compare Lewis and Full corrections, and evaluate their effects on single-, double-, and triple-channel dosimetry. Methods:Seven films were scanned at seven lateral positions using a cyclic-shift design. For each position and RGB channel, center-equivalent response was modeled as PVc = A + B * PV. Lewis correction used two films with linear interpolation of A and B; Full correction used all center-local pairs with PCHIP interpolation of PVc - PV. Performance was assessed by portrait-landscape profile consistency and dose accuracy. Results: LRA was affine in PV, asymmetric about scanner center, and dependent on film model and channel. Both corrections reduced profile differences. Mean absolute profile differences across MU levels ranged from 1.4%-5.3% for EBT4 and 2.4%-6.8% for EBT-XD. The methods performed similarly for EBT4, while Full correction reduced discrepancies for several EBT-XD double- and triple-channel methods. Residual blue-channel errors limited blue, red-blue, and triple-channel performance. At 500 MU and above, red showed the best dose agreement; at 100 MU, both corrections increased deviations for several single-channel estimates. Full correction produced smaller deviations than Lewis in several EBT-XD conditions. Conclusions:LRA should be corrected in the raw-PV domain before dose reconstruction. Full correction better preserved profile consistency and dose accuracy, particularly for EBT-XD. Because improved profile consistency did not always improve central-dose agreement, both should be evaluated separately in commissioning.

physics.med-ph↗

arXiv2026

Dosimetric Quantification of a Commercial Dual-Tube kV X-Ray System for Preclinical FLASH Research

A kV dual tube system has been disseminated as a commercial research platform for preclinical FLASH radiotherapy (RT). Because the tubes are arranged in a parallel opposed geometry, both output symmetry and time resolved tube synchronization are critical for achieving sufficiently high dose rates (DR) and reproducible study results. We quantified tube output asymmetry observed in depth dose measurements as well as tube synchronization and evaluated their impact on FLASH studies. The dual-tube system defines dose per pulse as the combined single pulse output from both tubes, with DR given by dose per pulse/pulse length. 3D dose distributions were reconstructed from film measurements to assess the impact of output discrepancies. Pulse synchronization between tubes was characterized using a scintillator with 1 ms resolution. We showed >20% discrepancies in output at nominally equal mA/ms settings. After we compensated such discrepancy by decreasing the current of the tube with higher output, the inter tube output difference was reduced to <1%, restoring symmetrical depth dose. We further simulated an in vivo intestinal irradiation in which naive tube settings resulted in >22% of the organ volume receiving >102% of the prescribed dose, compared with <7% when output compensation was applied. We identified a 10.2 +/- 7.0ms synchronization jitter between tubes, which disproportionately impacts the DR at low dose-per-pulse settings, particularly relevant for fractionated studies. Corresponding quality assurance (QA) was designed to monitor tube synchronization over time. We quantified the dosimetric impact of asymmetric output and synchronization and demonstrated implications for preclinical studies. The proposed methodology and QA would mitigate and monitor these effects, ensuring study reproducibility.

physics.med-ph↗

arXiv2025

An image-guided high-precision research platform for ultra-high dose rate spinal cord toxicity studies

Objective: While FLASH radiotherapy is recognized for short-term normal tissue sparing, its durability in late-responding organs remains uncertain, limiting clinical adoption. With its clinical importance and steep dose-response, the spinal cord is an ideal model for evaluating FLASH effect on late toxicity. This work introduces a robust image-guided research platform for high-precision irradiation at both CONV and UHDR to enable FLASH late toxicity studies using a rat spinal cord model. Approach: A modified LINAC was employed to irradiate the C1-T2 rat spinal cord with 18 MeV UHDR and CONV beams. A custom rat immobilization device, a portable X-ray imaging system, and an ion-chamber-based UHDR output monitoring system were integrated to ensure accurate C1-T2 localization and precise dose delivery. A Monte Carlo (MC) dose engine was developed to provide accurate dosimetry and support interpretation of in vivo results. Scintillator measurements were performed within the spinal cord to verify MC results and the precision of our platform. Results: We achieved submillimeter C1-T2 setup accuracy and maintained submillimeter intrafraction motion. Ion chamber readings showed linear correlation with UHDR output. MC indicated uniform irradiation along the central ~13 mm cord. Our CONV beam exhibited distribution close to that of the UHDR beam, with difference <3%, isolating dose rate as the only variable. Scintillator-measured dose agreed with MC within 4%, confirming both MC accuracy and the platform's high-precision delivery. Significance: We developed the first comprehensive, image-guided preclinical platform for accurate UHDR and CONV irradiation to investigate FLASH-mitigated spinal cord toxicity in rats. This work thus establishes a robust foundation for systematic evaluation of the FLASH effect in late-responding organs and for determining clinical applicability of FLASH.

physics.med-ph↗

arXiv2025

Comprehensive characterization and validation of a fast-resolving (1000 Hz) plastic scintillator for ultra-high dose rate electron dosimetry

Background: The normal tissue sparing effect of ultra-high dose rate irradiation (>40 Gy/s, UHDR), as compared to conventional dose rate (CONV), has attracted significant research interest for FLASH radiotherapy (RT). Accurate, dose rate independent, fast-responding dosimeters capable of resolving the spatiotemporal characteristics of UHDR beams are urgently needed to facilitate FLASH research and support its clinical translation. Tissue-equivalent scintillators, with millimeter-level spatial resolution and millisecond-level temporal resolution, possess these required characteristics and show strong potential for use in UHDR dosimetry. Purpose: We investigated the performance of the HYPERSCINT RP-FLASH scintillator system at up to 1000 Hz sampling frequency (fs) for UHDR electron beam dosimetry. Methods: The scintillator was exposed to CONV and UHDR electron irradiation using a LINAC-based FLASH platform. Its spectral characteristics were delineated with a four-component calibration, followed by a signal-to-dose calibration using 18 MeV CONV electron beam. The dose linearity and dosimetric accuracy in response to CONV and UHDR irradiation at 1 and 1000 Hz fs were quantified against ion chamber and EBT-XD film measurements. The response of the scintillator system was investigated as a function of beam energy (6 and 18 MeV), field size (2x2 to 25x25 cm2), dose per pulse (DPP, 0.8 to 2.3 Gy/pulse), and pulse repetition frequency (PRF, 30 to 180 Hz). Relative signal sensitivity was quantified against accumulated dose to account for the scintillator's radiation degradation. Pulse-resolved dose measurements at 18 MeV UHDR, obtained using the scintillator with 1000 Hz fs for a train of 10 pulses at 180 Hz PRF, were validated with a PMT-fiber optic scattered radiation detector.

physics.med-ph↗

arXiv2025

A universal bioluminescence tomography system for pre-clinical image-guided radiotherapy research

CBCT-guided small animal irradiators encounter challenges in localizing soft-tissue targets due to low imaging contrast. Bioluminescence tomography (BLT) offers a promising solution, but they have largely remained in laboratorial development, limiting accessibility for researchers. In this work, we develop a universal, commercial-graded BLT-guided system (MuriGlo) designed to seamlessly integrate with commercial irradiators and empower researchers for translational studies. We demonstrate its capabilities in supporting in vitro and in vivo studies. The MuriGlo comprises detachable mouse bed, thermostatic control, mirrors, filters, and CCD, enabling multi-projection and multi-spectral imaging. We evaluate that the thermostatic control effectively sustains animal temperature at 37°C throughout imaging, and quantify that the system can detect as few as 61 GL261-AkaLuc cells in vitro. To illustrate how the MuriGlo can be utilized for in vivo image-guided research, we present 3 strategies, BLT-guided 5-arc, 2-field box, and BLI-guided single-beam, ranging from complicated high-conformal to simplest high-throughput plans. The high conformal BLT-guided 5-arc plan fully covers the gross tumor volume (GTV) at prescribed dose with minimal normal tissue exposure (3.9%), while the simplified, high-throughput BLT-guided 2-field box achieves 100% GTV coverage but results in higher normal tissue exposure (13.1%). Moreover, we demonstrate that the localization accuracy of MuriGlo for both widely-used SARRP and SmART irradiators is within1 mm, and the tumor coverage reaches over 97% with 0.75mm margin. The universal BLT-guided system offers seamless integration with commercial irradiators, achieving comparable localization accuracy, expected to supporting high-precision radiation research.

physics.med-ph↗

arXiv2024

Electron FLASH platform for pre-clinical research: LINAC modification, simplification of pulse control and dosimetry

Background: FLASH radiotherapy is a treatment regime that delivers therapeutic dose to tumors at an ultra-high dose rate while maintaining adequate normal tissue sparing. However, a comprehensive understanding of the underlying mechanisms, potential late toxicities, and optimal fractionation schemes is important for successful clinical translation. This has necessitated extensive pre-clinical investigations, leading several research institutions to initiate dedicated FLASH research programs. Purpose: This work describes a workflow for establishing an easily accessible electron FLASH (eFLASH) platform. The platform incorporates simplified pulse control, optimized dose rate delivery, and validated Monte Carlo (MC) dose engine for accurate in vivo dosimetry dedicated to FLASH pre-clinical studies. Methods: Adjustment of the automatic frequency control (AFC) module allowed us to optimize the LINAC pulse form to achieve a uniform dose rate. A MC model for the 6 MeV FLASH beam was commissioned to ensure accurate dose calculation necessary for reproducible in vivo studies. Results: Optimizing the AFC module enabled the generation of a uniform pulse form, ensuring consistent dose per pulse and a uniform dose rate throughout FLASH irradiation. The MC model closely agreed with film measurements. MC dose calculations indicated that 6 MeV FLASH is adequate to achieve a uniform dose distribution for mouse whole brain irradiation but may not be optimal for the spinal cord study. Conclusions: We present a novel workflow for establishing a LINAC-based eFLASH research platform, incorporating techniques for optimized dose rate delivery, a simplified pulse control system, and validated MC engine. This work provides researchers with valuable new approaches to facilitate the development of robust and accessible LINAC-based system for FLASH studies.

physics.med-ph↗

arXiv2020

Quantitative Bioluminescence Tomography-guided System for Conformal Irradiation In Vivo

Although cone-beam CT (CBCT) has been used to guide irradiation for pre-clinical radiotherapy(RT) research, it is limited to localize soft tissue target especially in a low imaging contrast environment. Knowledge of target shape is a fundamental need for RT. Without such information to guide radiation, normal tissue can be irradiated unnecessarily, leading to experimental uncertainties. Recognition of this need led us to develop quantitative bioluminescence tomography (QBLT), which provides strong imaging contrast to localize optical targets. We demonstrated its capability of guiding conformal RT using an orthotopic bioluminescent glioblastoma (GBM) model. With multi-projection and multi-spectral bioluminescence imaging and a novel spectral derivative method, our QBLT system is able to reconstruct GBM with localization accuracy <1mm. An optimal threshold was determined to delineate QBLT reconstructed gross target volume (GTV_{QBLT}), which provides the best overlap between the GTV_{QBLT} and CBCT contrast labeled GBM (GTV), used as the ground truth for the GBM volume. To account for the uncertainty of QBLT in target localization and volume delineation, we also innovated a margin design; a 0.5mm margin was determined and added to GTV_{QBLT} to form a planning target volume (PTV_{QBLT}), which largely improved tumor coverage from 75% (0mm margin) to 98% and the corresponding variation (n=10) of the tumor coverage was significantly reduced. Moreover, with prescribed dose 5Gy covering 95% of PTV_{QBLT}, QBLT-guided 7-field conformal RT can irradiate 99.4 \pm 1.0% of GTV vs. 65.5 \pm 18.5% with conventional single field irradiation (n=10). Our QBLT-guided system provides a unique opportunity for researchers to guide irradiation for soft tissue targets and increase rigorous and reproducibility of scientific discovery.

physics.med-ph↗

arXiv2003

Fluctuation and localization of acoustic waves in bubbly water

Here the fluctuation properties of acoustic localization in bubbly water is explored. We show that the strong localization can occur in such a system for a certain frequency range and sufficient filling fractions of air-bubbles. Two fluctuating quantities are considered, that is, the fluctuation of transmission and the fluctuation of the phase of acoustic wave fields. When localization occurs, these fluctuations tend to vanish, a feature able to uniquely identify the phenomenon of wave localization.

cond-mat.soft↗