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Daniel L. J. Thorek

Publications and source records attributed to Daniel L. J. Thorek.

6 recordsLinked to original sources

NGSE-Corr: A technique for objective clinical evaluation of quantitative-imaging methods without a gold standard

Objective evaluation of quantitative-imaging (QI) methods based on how reliably they measure true values is important for clinical translation. Performing such evaluation with patient data is highly desirable but hindered by the lack of gold standards. To address this challenge, advancing on previous studies, we propose a no-gold-standard evaluation technique, NGSE-Corr, that objectively evaluates QI methods without true values. The technique assumes a linear stochastic relationship between true and measured values, characterized by a slope, bias, and multivariate Gaussian-distributed noise term that models correlated noise across QI methods. We derive a maximum-likelihood approach to estimate these parameters using only measured values. From the estimates, we compute noise-to-slope ratio (NSR) to rank QI methods based on precision. Numerical experiments showed that NGSE-Corr reliably estimated the NSR, accurately ranked methods, and maintained performance even when assumptions made by the technique were partially violated. We also validated NGSE-Corr in an in silico imaging trial to rank three quantitative SPECT methods for measuring regional activity uptake in patients with bone metastatic castrate-resistant prostate cancer treated with radium-223. NGSE-Corr correctly identified the most precise QI method and ranked the methods for 95% (95% CI, 89%-98%) and 91% (95% CI, 84%-95%) of trials, respectively, with data from 50 patients. Performance further improved with larger cohorts. With 200 patients, NGSE-Corr yielded same rankings as those obtained with true values across all trial instances. These findings demonstrate the ability of NGSE-Corr to accurately rank QI methods without gold standards and motivate clinical validation and broader applications.

physics.med-ph↗

Progress in SPECT and PET Reconstruction for Theranostics: From Diagnosis to Therapy

The theranostic paradigm enables personalization of treatment by selecting patients with a diagnostic radiopharmaceutical and monitoring therapy using a matched therapeutic isotope. This strategy relies on accurate image reconstruction of both pretherapy and post-therapy images for patient selection and monitoring treatment. However, traditional reconstruction methods are hindered by challenges such as crosstalk in multi-isotope imaging and extremely low-count measurements data when imaging of alpha-emitting isotopes. Additionally, to fully realize the benefits of new imaging systems being developed for theranostic applications, advanced reconstruction techniques are needed. This review highlights recent progress and discusses critical challenges and unmet needs in theranostic image reconstruction.

physics.med-ph↗

Joint regional uptake quantification of Thorium-227 and Radium-223 using a multiple-energy-window projection-domain quantitative SPECT method

Thorium-227-based alpha-particle radiopharmaceutical therapies (α-RPTs) are being investigated in several clinical and pre-clinical studies. After administration, Thorium-227 decays to Radium-223, another alpha-particle-emitting isotope, which redistributes within the patient. Reliable dose quantification of both Thorium-227 and Radium-223 is clinically important, and SPECT may perform this quantification as these isotopes also emit X- and gamma-ray photons. However, reliable quantification is challenged by the orders-of-magnitude lower activity compared to conventional SPECT, resulting in a very low number of detected counts, the presence of multiple photopeaks, substantial overlap in the emission spectra of these isotopes, and the image-degrading effects in SPECT. To address these issues, we propose a multiple-energy-window projection-domain quantification (MEW-PDQ) method that jointly estimates the regional activity uptake of both Thorium-227 and Radium-223 directly using the SPECT projection from multiple energy windows. We evaluated the method with realistic simulation studies using anthropomorphic digital phantoms, in the context of imaging patients with bone metastases of prostate cancer and treated with Thorium-227-based α-RPTs. The proposed method yielded reliable (accurate and precise) regional uptake estimates of both isotopes and outperformed state-of-the-art methods across different lesion sizes and contrasts, in a virtual imaging trial, as well as with moderate levels of intra-regional heterogeneous uptake and with moderate inaccuracies in the definitions of the support of various regions. Additionally, we demonstrated the effectiveness of using multiple energy windows and the variance of the estimated uptake using the proposed method approached the Cramér-Rao-lower-bound-defined theoretical limit.

physics.med-ph↗

WIN-PDQ: A Wiener-estimator-based projection-domain quantitative SPECT method that accounts for intra-regional uptake heterogeneity

SPECT can enable the quantification of activity uptake in lesions and at-risk organs in α-particle-emitting radiopharmaceutical therapies (α-RPTs). But this quantification is challenged by the low photon counts, complicated isotope physics, and the image-degrading effects in α-RPT SPECT. Thus, strategies to optimize the SPECT system and protocol designs for the task of regional uptake quantification are needed. Objectively performing this task-based optimization requires a reliable (accurate and precise) regional uptake quantification method. Conventional reconstruction-based quantification (RBQ) methods have been observed to be erroneous for α-RPT SPECT. Projection-domain quantification methods, which estimate regional uptake directly from SPECT projections, have demonstrated potential in providing reliable regional uptake estimates, but these methods assume constant uptake within the regions, an assumption that may not hold. To address these challenges, we propose WIN-PDQ, a Wiener-estimator-based projection-domain quantitative SPECT method. The method accounts for the heterogeneity within the regions of interest while estimating mean uptake. An early-stage evaluation of the method was conducted using 3D Monte Carlo-simulated SPECT of anthropomorphic phantoms with radium-223 uptake and lumpy-model-based intra-regional uptake heterogeneity. In this evaluation with phantoms of varying mean regional uptake and intra-regional uptake heterogeneity, the WIN-PDQ method yielded ensemble unbiased estimates and significantly outperformed both reconstruction-based and previously proposed projection-domain quantification methods. In conclusion, based on these preliminary findings, the proposed method is showing potential for estimating mean regional uptake in α-RPTs and towards enabling the objective task-based optimization of SPECT system and protocol designs.

physics.med-ph↗

A list-mode multi-energy window low-count SPECT reconstruction method for isotopes with multiple emission peaks

SPECT provides a mechanism to perform absorbed-dose quantification tasks for $α$-particle radiopharmaceutical therapies ($α$-RPTs). However, quantitative SPECT for $α$-RPT is challenging due to the low number of detected counts, the complex emission spectrum, and other image-degrading artifacts. Towards addressing these challenges, we propose a low-count quantitative SPECT reconstruction method for isotopes with multiple emission peaks. Given the low-count setting, it is important that the reconstruction method extract the maximal possible information from each detected photon. Processing data over multiple energy windows and in list-mode (LM) format provide mechanisms to achieve that objective. Towards this goal, we propose a list-mode multi-energy window (LM-MEW) OSEM-based SPECT reconstruction method that uses data from multiple energy windows in LM format, and includes the energy attribute of each detected photon. For computational efficiency, we developed a multi-GPU-based implementation of this method. The method was evaluated using 2-D SPECT simulation studies in a single-scatter setting conducted in the context of imaging [$^{223}$Ra]RaCl${_2}$. The proposed method yielded improved performance on the task of estimating activity uptake within known regions of interest in comparison to approaches that use a single energy window or use binned data. The improved performance was observed in terms of both accuracy and precision and for different sizes of the region of interest. Results of our studies show that the use of multiple energy windows and processing data in LM format with the proposed LM-MEW method led to improved quantification performance in low-count SPECT of isotopes with multiple emission peaks. These results motivate further development and validation of the LM-MEW method for such imaging applications, including for $α$-RPT SPECT.

physics.med-ph↗

A projection-domain low-count quantitative SPECT method for alpha-particle emitting radiopharmaceutical therapy

Single-photon emission computed tomography (SPECT) provides a mechanism to estimate regional isotope uptake in lesions and at-risk organs after administration of α-particle-emitting radiopharmaceutical therapies (α-RPTs). However, this estimation task is challenging due to the complex emission spectra, the very low number of detected counts, the impact of stray-radiation-related noise at these low counts, and the multiple image-degrading processes in SPECT. The conventional reconstruction-based quantification methods are observed to be erroneous for α-RPT SPECT. To address these challenges, we developed a low-count quantitative SPECT (LC-QSPECT) method that directly estimates the regional activity uptake from the projection data, compensates for stray-radiation-related noise, and for the radioisotope and SPECT physics. The method was validated in the context of three-dimensional SPECT with 223 Ra. Validation was performed using both realistic simulation studies, including a virtual clinical trial, and synthetic and anthropomorphic physical-phantom studies. Across all studies, the LC-QSPECT method yielded reliable regional-uptake estimates and outperformed the conventional ordered subset expectation maximization (OSEM)-based reconstruction and geometric transfer matrix (GTM)-based post-reconstruction partial-volume compensation methods. Further, the method yielded reliable uptake across different lesion sizes, contrasts, and different levels of intra-lesion heterogeneity. Additionally, the variance of the estimated uptake approached the Cramé-Rao bound-defined theoretical limit.

physics.med-ph↗