- The document discusses the use of artificial intelligence and radiomics in radiation oncology. It presents frameworks for radiomics analysis involving image registration, tumor segmentation, feature extraction, and predictive modeling.
- Specific applications discussed include using radiomics for lung cancer screening and prediction of tumor response. Radiomics features combined with machine learning models show improved performance over clinical guidelines for assessing lung nodule malignancy.
- Methods are also presented for quantifying tumor characteristics like spiculation through image analysis and extracting interpretable radiomics features. This can provide semantic information to radiologists for assessment.
1.Aim of Radiotherapy
The goal of radiotherapy is to deliver a prescribed dose of radiation to the Target while sparing surrounding Healthy tissues to the largest extent possible
2.Organ Motion
Intra-fraction motion
during the fraction
Heartbeat
Swallowing
Coughing
Eye movement
Inter-fraction motion
- in between the fractions
Tumour change
Weight gain/loss
Positioning deviation
Breathing
Bowel and rectal filling
Bladder filling
Muscle relaxation/tension
3. Respiratory motion affects:
Respiratory motion affects all tumour sites in the thorax, abdomen and Pelvis. Tumours in the Lung, Liver, Pancreas, Oesophagus, Breast, Kidneys, prostate
Tumour displacement varies depending on the site and organ Location
Lung tumours can move several cm in any direction during irradiation
It is most prevalent and prominent in Lung cancers
4. Problems associated with respiratory motion during RT
Image acquisition limitations
Treatment planning limitations
Radiation delivery limitations
5. Methods to Account for Respiratory Motion
1. Motion encompassing methods
2. Respiratory gating methods
3. Breath hold methods
4. Forced shallow breathing with abdominal compression
5. Real-time tumor tracking methods
Summary:
The management of respiratory motion in radiation oncology is an evolving field
IGRT provides a solution for combating organ motion in radiotherapy
Delivering higher dose to tumor and less dose to normal tissue.
Limited clinical studies, needs to be studied further
IGRT – the future of radiotherapy
This is a made easy summary of ICRU 89 guidelines for gynecological brachytherapy. Extra practical questions for MD/DNB Radiotherapy exams are also attached.
EBCTCG METAANALYSIS
INDICATION OF POST OP RADIOTHERAPY
Immobilization devices
Conventional planning
Alignment of the Tangential Beam with the Chest Wall Contour
Doses To Heart & Lung By Tangential Fields
1.Aim of Radiotherapy
The goal of radiotherapy is to deliver a prescribed dose of radiation to the Target while sparing surrounding Healthy tissues to the largest extent possible
2.Organ Motion
Intra-fraction motion
during the fraction
Heartbeat
Swallowing
Coughing
Eye movement
Inter-fraction motion
- in between the fractions
Tumour change
Weight gain/loss
Positioning deviation
Breathing
Bowel and rectal filling
Bladder filling
Muscle relaxation/tension
3. Respiratory motion affects:
Respiratory motion affects all tumour sites in the thorax, abdomen and Pelvis. Tumours in the Lung, Liver, Pancreas, Oesophagus, Breast, Kidneys, prostate
Tumour displacement varies depending on the site and organ Location
Lung tumours can move several cm in any direction during irradiation
It is most prevalent and prominent in Lung cancers
4. Problems associated with respiratory motion during RT
Image acquisition limitations
Treatment planning limitations
Radiation delivery limitations
5. Methods to Account for Respiratory Motion
1. Motion encompassing methods
2. Respiratory gating methods
3. Breath hold methods
4. Forced shallow breathing with abdominal compression
5. Real-time tumor tracking methods
Summary:
The management of respiratory motion in radiation oncology is an evolving field
IGRT provides a solution for combating organ motion in radiotherapy
Delivering higher dose to tumor and less dose to normal tissue.
Limited clinical studies, needs to be studied further
IGRT – the future of radiotherapy
This is a made easy summary of ICRU 89 guidelines for gynecological brachytherapy. Extra practical questions for MD/DNB Radiotherapy exams are also attached.
EBCTCG METAANALYSIS
INDICATION OF POST OP RADIOTHERAPY
Immobilization devices
Conventional planning
Alignment of the Tangential Beam with the Chest Wall Contour
Doses To Heart & Lung By Tangential Fields
Radiomics Analysis of Pulmonary Nodules in Low Dose CT for Early Detection of...Wookjin Choi
Purpose: To predict the histopathologic subtypes with poor surgery prognosis in early stage lung adenocarcinomas using CT and PET radiomics.
Methods: We retrospectively enrolled 53 patients with stage I lung adenocarcinoma who underwent both diagnostic CT and 18F-fluorodeoxyglucose (FDG) PET/CT before complete surgical resection of the tumors. Tumor segmentation was manually contoured by a physician on both the diagnostic CT and the attenuation CT of PET/CT.A total of 170 radiomics features were extracted on both PET and CT images to design predictive models for two histopathologic endpoints: (1) tumors with solid or micropapillary predominant subtype (aggressiveness), and (2) tumors with micropapillary component more than 5% (MIP5). We used least absolute shrinkage and selection operator (LASSO) as a model building method coupled with a class separability feature selection (CSFS) method. For an unbiased model estimate, a 10-fold cross validation approach was used. The area under the curve (AUC) and prediction accuracy were employed to evaluate the performance of the model. P-values were computed using Wilcoxon rank-sum test.
Results: Of the 53 patients, 9 and 15 had tumors with aggressiveness and MIP5, respectively. For both endpoints, LASSO models with two PET radiomics features achieved the best performance. For aggressiveness, the LASSO model with PET Cluster Shade and PET 2D Variance resulted in 77.6±2.3% accuracy and 0.71±0.02 AUC (P = 0.011). For MIP5, the LASSO model with PET Eccentricity and PET Cluster Shade resulted in 69.6±3.1% accuracy and 0.68±0.04 AUC (P=0.014). The PET Cluster Shade was commonly selected in both models. Cluster shade is a texture feature that measures the skewness of the co-occurrence matrix. Higher PET cluster shade predicted that the tumor was more aggressive and more likely MIP5.
Conclusion: We showed that PET/CT radiomics features can predict tumor aggressiveness.
Funding Support, Disclosures, and Conflict of Interest: This work was supported in part by the National Cancer Institute Grants R01CA172638.
American Association for Cancer Research Annual Meeting 2022
Analysis of images of routinely acquired tissue specimens promise to provide biomarkers that can be used to predict disease outcome and steer treatment, improve diagnostic reproducibility, and reveal new insights to further advance current human understanding of disease. The advent of AI and ubiquitous high-end computing are making it possible to carry out accurate whole slide image morphological and molecular tissue analyses at cellular and subcellular resolutions. AI methods are can enable exploration and discovery of novel diagnostic biomarkers grounded in prognostically predictive spatial and molecular patterns as well as quantitative assessments of predictive value and reproducibility of traditional morphological patterns employed in anatomic pathology. AI methods may be adapted to help steer treatment through integrative analysis of clinical information along with Pathology, Radiology and molecular data.
Interpretable Spiculation Quantification for Lung Cancer ScreeningWookjin Choi
Spiculations are spikes on the surface of pulmonary nodule and are important predictors of malignancy in lung cancer. In this work, we introduced an interpretable, parameter-free technique for quantifying this critical feature using the area distortion metric from the spherical conformal (angle-preserving) parameterization. The conformal factor in the spherical mapping formulation provides a direct measure of spiculation which can be used to detect spikes and compute spike heights for geometrically-complex spiculations. The use of the area distortion metric from conformal mapping has never been exploited before in this context. Based on the area distortion metric and the spiculation height, we introduced a novel spiculation score. A combination of our spiculation measures was found to be highly correlated (Spearman's rank correlation coefficient ρ = 0.48) with the radiologist's spiculation score. These measures were also used in the radiomics framework to achieve state-of-the-art malignancy prediction accuracy of 88.9% on a publicly available dataset.
Societal Impact of Applied Data Science on the Big Data StackStealth Project
Data availability should ideally improve accountability and decision processes. Armed with evidence of data science working across multiple domains from healthcare analytics to internet advertising big data is enabling changes in society, one application at a time. This talk will have two parts. We will first present a data scientist's overview of different technologies in use today and their utility.
Then we will do a deep-dive on specific implementation and challenges we addressed while working with multiple partners in the healthcare industry on real-world healthcare data. We will discuss and demonstrate prototypes of our solutions for cost prediction and risk-of-readmission care management, and how we leveraged big data machine learning frameworks. We will end with an open conversation about challenges in verticals other than healthcare and provide an overview of ongoing efforts for social good at the University of Washington Center for Data Science; each a story in its own.
Deep Learning-based Histological SegmentationDifferentiates Cavitation Patte...Wookjin Choi
Unsupervised segmentation (unlabeled regions of interest, ROIs) and autoencoder (AE)-based classification were used to classify differences in cavitation patterns in knees and digits using the stained images (n=20-30 images/group).
Each image was divided into 256 x 256 pixel patches, and a convolutional neural network (CNN)-based unsupervised segmentation was used to identify ROIs. These patches were subsequently fed into a CNN-based AE whose latent space layer was connected to a classifier for input patch classification.
The AE was trained using the ROIs identified by the unsupervised segmentation, and the image classes were used to train the classifier. Whole image classifications were determined by maximum voting of the patch results and evaluated by accuracy.
Artificial Intelligence To Reduce Radiation-induced Cardiotoxicity In Lung Ca...Wookjin Choi
Traditionally, radiation-induced cardiotoxicity has been studied using cardiac radiation doses rather than functional imaging. We developed artificial intelligence (AI) models based on novel cardiac delta radiomics using pre- and post-treatment FDG-PET/CT scans to predict overall survival in lung cancer patients undergoing radiotherapy. We identified four clinically relevant delta radiomics features with the AI prediction models. The best model achieved an AUC of 0.91 on the training set and 0.87 on the test set. We are a pioneering group in AI for functional cardiac imaging. If validated, this approach will enable to use standard PET/CT scans as functional cardiac imaging with good predictive AUC for OS, as well as provide automated methods to provide functional cardiac information for clinical outcome prediction AI in lung cancer patients.
Novel Functional Radiomics for Prediction of Cardiac PET Avidity in Lung Canc...Wookjin Choi
Purpose/Objective(s)
Traditional methods of evaluating cardiotoxicity focus solely on radiation doses to the heart and do not incorporate functional imaging information. Functional imaging has great potential to improve the ability to provide early prediction for cardiotoxicity for lung cancer patients undergoing radiotherapy. FDG-based PET/CT imaging is routinely obtained as part of standard staging work up for lung cancer patients. Although FDG PET/CT scans are typically used to evaluate the tumor, imaging guidelines note that FDG PET/CT scans are an FDA-approved method to image for cardiac inflammation, and studies have noted that the PET cardiac signal can be predictive of clinical outcomes. The purpose of this work was to develop a radiomics model to predict clinical cardiac assessment of standard of care FDG PET/CT scans.
Materials/Methods
The study included 100 consecutive lung cancer patients treated with radiotherapy who underwent standard pre-treatment FDG-PET/CT staging scans. A clinician reviewed the PET/CT scans per clinical cardiac assessment guidelines and classified the cardiac uptake as: 0 = uniform diffuse, 1 = absent, 2 = heterogeneous, with event rates of 20%, 44%, and 35%, respectively. The heart was delineated and 200 novel functional radiomics features were selected to classify cardiac FDG uptake patterns. We divided the data into an 80% training set and a 20% test set to train and evaluate the classification models. Feature reduction was carried out using the Wilcoxon test (with Bonferroni adjusted p<0.05), hierarchical clustering, and Recursive Feature Elimination. Two automatic machine learning (AutoML) frameworks were used to determine classification models: a Random Forest Classifier (Tree-based Pipeline Optimization Tool, TPOT) and Linear Discriminant Analysis (AutoSklearn). 10-fold cross validation was carried out for training and the accuracy of the ability of the models to predict for clinical cardiac assessment is reported.
Results
Fifty-one independent radiomics features were reduced to 3 clinically pertinent features (PET 2D Skewness, PET Grey Level Co-occurrence Matrix Correlation, and PET Median) using feature reduction techniques. The model selected by TPOT showed 89.8% predictive accuracy in the cross validation of the training set and 85% predictive accuracy on the test set. The model selected by AutoSklearn showed 89.7% predictive accuracy in the cross validation of the training set and 80% predictive accuracy on the test set.
Conclusion
The novelty of this work is that it is the first study to develop and evaluate functional cardiac radiomic features from standard of care FDG PET/CT scans with the data showing good predictive accuracy with clinical imaging evaluation. If validated, the current work provides automated methods to provide functional cardiac information using standard of care imaging that can be used as an imaging biomarker for early clinical toxicity prediction for lung cancer patients.
Novel Deep Learning Segmentation Models for Accurate GTV and OAR Segmentation...Wookjin Choi
Purpose/Objective(s)
MR-guided adaptive radiotherapy (MRgART) improves target coverage and organ-at-risk (OAR) sparing in pancreatic cancer radiation therapy (RT). Inter-fractional changes in patients undergoing RT require time intensive re-delineation of gross tumor volume (GTV) and OARs prior to adaptive optimization. Accurate automatic segmentation has the potential to significantly improve efficiency of the adaptive workflow. We hypothesized that state-of-the-art deep learning (DL) segmentation models could adequately segment GTV and OARs in both planning and daily fractional MR scans.
Materials/Methods
The study included 21 patients with pancreatic cancer treated with MRgART (10 Gy x 5 fractions). The planning MR as well as all daily MR images and registrations were collected (6 image sets per patient and a total of 126 image sets). The planning MR and fraction 1-4 image sets were used as the training set (N = 105), while the test set (N = 21) comprised images for fraction 5, to simulate the last step of incremental learning from planning to final fraction. Evaluated contours included the GTV, Small Bowel, Large Bowel, Duodenum, Left and Right Kidney, Liver, Spinal Cord, and Stomach. To mimic clinical conditions, contour accuracy was evaluated within the ring structure surrounding the PTV, inside of which daily adaptive re-contouring is applied (2 cm expansion in the cradio-caudal direction, 3 cm expansion otherwise). We evaluated three DL model architectures: SegResNet, SegResNet 2D, and SwinUNETR to autosegment GTV and OARs. The segmentation models were trained on the training set using 5-fold cross-validation (CV) and quantitatively analyzed by comparing against clinically used contours with DICE scores. Qualitative analysis was performed by a radiation oncologist using a scoring scale: 1 = perfect, 2 = minor discrepancy, 3 = moderate discrepancy, and 4 = rejected.
Results
Overall, the DL segmentations were in acceptable agreement with clinical contours. The best performing model was the SwinUNETR model with overall training DICE = 0.88±0.06, test DICE = 0.78±0.11, and qualitative score of 1.6±0.8. The agreement between the DL model and clinical segmentation for the GTV was 0.79±0.08, with a qualitative score of 2.2±0.9
Conclusion
We report here the most comprehensive work on DL segmentation for pancreatic cancer MRgART, including quantitative and clinically-pertinent qualitative evaluations of 126 image sets and 3 DL architectures. Our data show good quantitative agreement between DL and clinical contours, and acceptable clinician evaluations for the majority of GTVs and OARs. The current work has great potential to significantly reduce a major bottleneck in the MRgART workflow for pancreatic cancer patients.
Novel Functional Delta-Radiomics for Predicting Overall Survival in Lung Canc...Wookjin Choi
AAPM2023_SU-300-IePD-F6-4
Purpose: Traditional methods of evaluating cardiotoxicity rely on cardiac radiation doses and do not incorporate functional imaging. Cardiac functional imaging can improve the ability to provide early prediction for clinical outcomes for lung cancer patients undergoing radiotherapy. FDG-based PET/CT imaging is routinely obtained for staging and disease assessment after treatment. Although FDG PET/CT scans are typically used to evaluate the tumor, studies have shown that the PET cardiac signal is predictive of clinical outcomes. Our study aimed to develop novel functional cardiac delta radiomics using pre and post-treatment FDG PET/CT scans to predict for overall survival (OS).
Methods: We conducted a study of 109 lung cancer patients who underwent standard FDG-PET/CT scans pre- and post-radiotherapy. Data from ACRIN 6668 (N=70) and an investigator-initiated lung cancer trial (N=39) for functional avoidance radiotherapy were used. The heart was delineated, and 200 cardiac CT and PET functional radiomics features were selected. Delta radiomics was calculated as the change between pre- and post-PET/CT. The data were divided into 80%/20% training/test set, and feature reduction was performed using Wilcoxon test, hierarchical clustering, and recursive feature elimination. A Gradient Boosting Classifier machine learning model evaluated the ability of the delta PET/CT cardiac radiomics to predict for OS using 10-fold cross-validation for training and area-under-the-curve (AUC) for model assessment.
Results: Median survival was 431 days (range 144 to 1640 days). 4 clinically relevant delta features were identified: pre-CT_Maximum, post-CT_Minimum, delta-CT_GLRM_Run_Variance, delta-PET_GLRM_Run_Entropy. The model showed an AUC of 0.91 on the training set and an AUC of 0.87 on the test set.
Conclusion: This is the first study to evaluate functional cardiac delta radiomic features from standard PET/CT scans with data showing good predictive AUC for OS. If validated, this work provides automated methods to provide functional cardiac information for clinical outcome prediction in lung cancer patients.
Automatic motion tracking system for analysis of insect behaviorWookjin Choi
Undergraduate research.
We present a multi-object tracking system to track small insects such as ants and bees. Motion-based object tracking recognizes the movements of objects in videos using information extracted from the given video frames. We applied several computer vision techniques, such as blob detection and appearance matching, to track ants. Moreover, we discussed different object detection methodologies and investigated the various challenges of object detection, such as illumination variations and blob merge/split. The proposed system effectively tracked multiple objects in various environments.
Assessing the Dosimetric Links between Organ-At-Risk Delineation Variability ...Wookjin Choi
Purpose: To determine the relative dosimetric impact of delineation variability (DV) when inter-observer and inter-technique planning variability (PV), and setup variability (SV) with are considered.
Methods: 409 plans for a single head-and-neck patient from the 2017 Radiation Knowledge plan competition were used. Plans were created with Eclipse (N=227), Pinnacle (N=49), RayStation (N=25), Monaco (N=75), and TomoTherapy (N=33) with delivery techniques conventional linac IMRT (N=142), volumetric modulated arc therapy (VMAT, N=234), and helical TomoTherapy (N=33). All plans were optimized using a consistent set of target volumes and a single OAR structure set. Four additional OAR structure sets were contoured by radiation oncologists (N=2) and medical physics residents (N=2) who had completed head-and-neck contouring training. Probabilistic DVHs, dose-volume coverage maps (DVCM), which shows the probability of achieving a dose metric, were computed for each OAR on the following scenarios: SV alone (N=1000), SV+PV (N=1000*409), SV+DV (N=1000*5), SV+PV+DV (total variability [TV], N=1000*409*5). Analysis focused on the probability of exceeding the maximum dose constraint exceeded 5% for each OAR.
Results: The primary source of variability was PV, which was expected due to inter-observer planning abilities and preferences during the optimization planning process, even when all participants utilized the same constraints. The parotid had the most significant interquartile range (IQR) on the PV scenario. Conversely, adding SV, DV, and TV each reduced the IQR, showing a washing out effect on the DVCM.
Conclusion: Assessment of OAR sensitivity to DV will be highly sensitive to the specific planning technique and planner, likely requiring plan-specific assessment of in-tolerance delineation variations. Incorporation SV and DV variabilities in plan assessments washes out their relative impacts on maximum dose.
Simulation of Realistic Organ-At-Risk Delineation Variability in Head and Nec...Wookjin Choi
(Sunday, 7/14/2019) 4:00 PM - 5:00 PM
Room: 225BCD
Purpose: To simulate realistic manual delineation (MD) organ-at-risk (OAR) delineation variability (DV) the purpose of quantifying DV’s dosimetric impact.
Methods: Fourteen independent MD head-and-neck OAR structure sets (SS) were obtained from the ESTRO Falcon group. Seven OARs were available (BrainStem, Esophagus, OralCavity, Parotid_L, Parotid_R, SpinalCord, and Thyroid). A consensus MD SS was generated by the simultaneous truth and performance level estimation (STAPLE) method. MD DV was evaluated with respect to the STAPLE SS using the Dice coefficient and Hausdorff distance (HD) geometric similarity metrics. DVs were simulated using auto-delineation (AD)
methods: an average surface of standard deviation (ASSD) method, GrowCut segmentation, and a random walker (RW) segmentation. Each OAR AD was repeated five times with a different seed or variability level. Dice and HD were computed for each OAR AD with respect to the STAPLE SS. Dosimetric analysis was achieved by intercomparing dose-volume histograms (DVH) from a plan developed with a reference MD SS with DVHs for each MD and AD. DVH confidence bands are reported for MD and each AD method.
Results: The MD Dice was 0.7±0.2 (μ±σ). AD Dice values (ASSD, GrowCut, and RW) were 0.5±0.2, 0.7±0.2, and 0.8±0.1, respectively. HDs were 35.4±45.2, 27.3±19.1, 29.3±19.9, and 14.6±10.3. The simulated DV increased with increasing the seed standard deviations or variability level. The dosimetric effect was largest for MD DVs (larger OAR DVH confidence intervals and larger HD), even though the MD Dice was greater than the ASSD and GrowCut Dice values. GrowCut DV resulted in less dosimetric variation than RW, unlike the geometric indices.
Conclusion: We developed a framework to simulate DVs and demonstrated its feasibility. ADs were able to simulate different magnitudes of DVs, but did not replicate the dosimetric consequences of human delineation variability. The correlation between geometric similarity metrics and dosimetric consequences of DV is poor.
Quantitative image analysis for cancer diagnosis and radiation therapyWookjin Choi
1.Lung Cancer Screening
1.1.Deep learning (feasible but not interpretable)
1.2.Radiomics (concise model)
1.3.Spiculation quantification (interpretable feature)
2.PET/CT Tumor Response
2.1.Aggressive Lung ADC subtype prediction (helpful for surgeons)
2.2.Pathologic response prediction (accurate but not concise)
2.3.Local tumor morphological changes (accurate and interpretable)
Interpretable Spiculation Quantification for Lung Cancer ScreeningWookjin Choi
Spiculations are spikes on the surface of pulmonary nodule and are important predictors of malignancy in lung cancer. In this work, we introduced an interpretable, parameter-free technique for quantifying this critical feature using the area distortion metric from the spherical conformal (angle-preserving) parameterization. The conformal factor in the spherical mapping formulation provides a direct measure of spiculation which can be used to detect spikes and compute spike heights for geometrically-complex spiculations. The use of the area distortion metric from conformal mapping has never been exploited before in this context. Based on the area distortion metric and the spiculation height, we introduced a novel spiculation score. A combination of our spiculation measures was found to be highly correlated (Spearman's rank correlation coefficient ρ = 0.48) with the radiologist's spiculation score. These measures were also used in the radiomics framework to achieve state-of-the-art malignancy prediction accuracy of 88.9% on a publicly available dataset.
Quantitative Image Analysis for Cancer Diagnosis and Radiation TherapyWookjin Choi
1.Lung Cancer Screening
1.1.Deep learning (feasible but not interpretable)
1.2.Radiomics (concise model)
1.3.Spiculation quantification (interpretable feature)
2.PET/CT Tumor Response
2.1.Aggressive Lung ADC subtype prediction (helpful for surgeons)
2.2.Pathologic response prediction (accurate but not concise)
2.3.Local tumor morphological changes (accurate and interpretable)
Robust Normal Lung CT Texture Features for the Prediction of Radiation-Induce...Wookjin Choi
Abstract
Purpose: Normal lung CT texture features have been used for the prediction of radiation-induced lung disease (RILD) - pneumonitis and fibrosis. For these features to be clinically useful, they should be robust (relatively invariant or unbiased) to tumor size variations and not correlated (non-redundant) with the normal lung volume of interest, i.e., volume of the peri-tumoral region.
Methods: CT images of 14 lung cancer patients were studied. Different sizes of gross tumor volumes (GTVs) were simulated with spheres (diameters 10 to 60 mm) and placed in the lung contralateral to the tumor. 27 texture features [nine from intensity histogram, eight from the gray-level co-occurrence matrix (GLCM) and ten from the gray-level run-length matrix (GLRM)] were extracted from the peri-tumoral region (uniform 30 mm expansion around the GTV in the lung). The Bland-Altman analysis was applied to measure the normalized range of agreement (nRoA) for each feature when GTV size varied. A feature was considered as robust when its nRoA was less than the threshold (100%), which was chosen at the nRoA of the volume of the peri-tumoral region with modification based on the cumulative graph of features vs. nRoA. A feature was regarded as not correlated with the volume of the peri-tumoral region when their correlation was lower than 0.70.
Results: 16 of the 27 texture features were identified as robust. All intensity histogram features were robust except sum and kurtosis. All GLCM features were robust except cluster shade, cluster prominence, and Haralick's Correlation. Five GLRM features (two run emphasis and three high gray-level emphasis) were robust while the other five (two nonuniformity and three low gray-level emphasis) were unrobost. None of the robust features was correlated with the volume of the peri-tumoral region. No feature showed statistically significant differences (P<0.05) on GTV location (upper vs. lower lobe).
Conclusion: We identified 16 robust normal lung CT texture features that can be further examined for the prediction of RILD. Particularly, GLRM high gray-level emphasis features were robust and characterized the radiologic manifestations of pulmonary abnormalities.
Robust Normal Lung CT Texture Features for the Prediction of Radiation-Induce...Wookjin Choi
Abstract
Purpose/Objective(s)
Normal lung CT texture features have been used for the prediction of radiation-induced lung disease (RILD) - pneumonitis and fibrosis. For these features to be clinically useful, they need to be relatively invariant (robust) to tumor size and not correlated with normal lung volume.
Materials/Methods
The free-breathing CTs of 14 lung SBRT patients were studied. Different sizes of GTVs were simulated with spheres (diameters 10 to 60 mm) placed in the lung contralateral to the tumor. Twenty-seven texture features (9 from intensity histogram, 8 from the gray-level co-occurrence matrix [GLCM], and 10 from the gray-level run-length matrix [GLRM]) were extracted from [lung – GTV]. The Bland-Altman method was applied to measure the normalized range of agreement (nRoA) of each texture feature when GTV size varied. A feature was considered as robust when its nRoA was less than that of [lung – GTV] volume (8.8%) and regarded as not correlated when their absolute correlation coefficient was lower than 0.70.
Results
Eighteen texture features were identified as robust. All intensity histogram features were robust except sum and kurtosis. All GLCM features were robust except energy and Haralick's Correlation. Five GLRM features (two run emphasis and three high gray-level emphasis) were robust while the other five (two nonuniformity and three low gray-level emphasis) were nonrobust. Particularly, all three low gray-level emphasis features had extremely large nRoAs (∼30%), indicating huge variations when GTV size changed. None of the robust features was correlated with the normal lung [lung – GTV] volume, suggesting that they can provide additional information. Three nonrobust features (sum and two nonuniformity features) were highly correlated with the normal lung volume. None feature showed statistically significant differences (P < 0.05) with respect to GTV location (upper vs. lower lobe).
Conclusion
We identified 18 robust lung CT texture features which were invariant to varying tumor volumes. Particularly the three GLRM high gray-level emphasis features can characterize the radiologic manifestations of pulmonary abnormalities. Hence these features can be further examined for the prediction of the RILD.
Aggressive Lung Adenocarcinoma Subtype Prediction Using FDG-PET/CT RadiomicsWookjin Choi
Purpose: To predict the histopathologic subtypes with poor surgery prognosis in early stage lung adenocarcinomas using CT and PET radiomics.
Methods: We retrospectively enrolled 53 patients with stage I lung adenocarcinoma who underwent both diagnostic CT and 18F-fluorodeoxyglucose (FDG) PET/CT before complete surgical resection of the tumors. Tumor segmentation was manually contoured by a physician on both the diagnostic CT and the attenuation CT of PET/CT.A total of 170 radiomics features were extracted on both PET and CT images to design predictive models for two histopathologic endpoints: (1) tumors with solid or micropapillary predominant subtype (aggressiveness), and (2) tumors with micropapillary component more than 5% (MIP5). We used least absolute shrinkage and selection operator (LASSO) as a model building method coupled with a class separability feature selection (CSFS) method. For an unbiased model estimate, a 10-fold cross validation approach was used. The area under the curve (AUC) and prediction accuracy were employed to evaluate the performance of the model. P-values were computed using Wilcoxon rank-sum test.
Results: Of the 53 patients, 9 and 15 had tumors with aggressiveness and MIP5, respectively. For both endpoints, LASSO models with two PET radiomics features achieved the best performance. For aggressiveness, the LASSO model with PET Cluster Shade and PET 2D Variance resulted in 77.6±2.3% accuracy and 0.71±0.02 AUC (P = 0.011). For MIP5, the LASSO model with PET Eccentricity and PET Cluster Shade resulted in 69.6±3.1% accuracy and 0.68±0.04 AUC (P=0.014). The PET Cluster Shade was commonly selected in both models. Cluster shade is a texture feature that measures the skewness of the co-occurrence matrix. Higher PET cluster shade predicted that the tumor was more aggressive and more likely MIP5.
Conclusion: We showed that PET/CT radiomics features can predict tumor aggressiveness.
Funding Support, Disclosures, and Conflict of Interest: This work was supported in part by the National Cancer Institute Grants R01CA172638.
Individually Optimized Contrast-Enhanced 4D-CT for Radiotherapy Simulation in...Wookjin Choi
Purpose/Objectives: To develop an individually optimized contrast-enhanced (CE) 4D-CT for radiotherapy simulation in pancreatic adenocarcinoma (PDA).
Materials/Methods: Ten PDA patients were enrolled and underwent three CT scans: a 4D-CT immediately following a CE 3D-CT, and an individually optimized CE 4D-CT using a test injection to estimate the peak contrast enhancement time and to optimize the delay time. Three physicians contoured the tumor and pancreatic tissues. We compared image quality scores, tumor volume, motion, image noise, tumor-to-pancreas contrast, and contrast-to- noise ratio (CNR) in the three CTs. We also evaluated inter-observer variations in contouring the tumor using simultaneous truth and performance level estimation (STAPLE).
Results: The average image quality scores for CE 3D-CT and CE 4D-CT were comparable (4.0 and 3.8, p=0.47), and both were significantly better than that for 4D-CT (2.6, p<0.001). The tumor-to- pancreas contrast in CE 3D-CT and CE 4D-CT were comparable (15.5 and 16.7 HU, p=0.71), and the later was significantly higher than that in 4D-CT (9.2 HU, p=0.03). Image noise in CE 3D-CT (12.5 HU) was significantly lower than that in CE 4D-CT (22.1 HU, p<0.001) and 4D-CT (19.4 HU, p=0.005). The CNR in CE 3D-CT and CE 4D-CT were comparable (1.4 and 0.8, p=0.23), and the former was significantly better than that in 4D-CT (0.6, p=0.04). The average tumor volume was smaller in CE 3D-CT (29.8 cm 3 ) and CE 4D-CT (22.8 cm 3 ) than in 4D-CT (42.0 cm 3 ), though the differences were not statistically significant. The tumor motion was comparable in 4D-CT and CE 4D-CT (7.2 and 6.2 mm, p=0.23). The inter-observer variations were comparable in CE 3D-CT and CE 4D-CT (Jaccard index 66.0% and 61.9%), and the former was significantly smaller than that of 4D-CT (55.6%, p=0.047).
Conclusions: The CE 4D-CT demonstrated largely comparable characteristics to the CE 3D-CT. It has high potential for simultaneously delineating the tumor and quantifying the tumor motion with a single scan.
Individually Optimized Contrast-Enhanced 4D-CT for Radiotherapy Simulation in...Wookjin Choi
To develop an individually optimized contrast-enhanced (CE) 4D-CT for radiotherapy simulation in pancreatic ductal adenocarcinomas (PDA).
http://scitation.aip.org/content/aapm/journal/medphys/43/6/10.1118/1.4958261
Identification of Robust Normal Lung CT Texture FeaturesWookjin Choi
Normal lung CT texture features have been used for the prediction of radiation-induced lung disease (radiation pneumonitis and radiation fibrosis). For these features to be clinically useful, they need to be relatively invariant (robust) to tumor size and not correlated with normal lung volume.
http://scitation.aip.org/content/aapm/journal/medphys/43/6/10.1118/1.4955803
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
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Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
Prix Galien International 2024 Forum ProgramLevi Shapiro
June 20, 2024, Prix Galien International and Jerusalem Ethics Forum in ROME. Detailed agenda including panels:
- ADVANCES IN CARDIOLOGY: A NEW PARADIGM IS COMING
- WOMEN’S HEALTH: FERTILITY PRESERVATION
- WHAT’S NEW IN THE TREATMENT OF INFECTIOUS,
ONCOLOGICAL AND INFLAMMATORY SKIN DISEASES?
- ARTIFICIAL INTELLIGENCE AND ETHICS
- GENE THERAPY
- BEYOND BORDERS: GLOBAL INITIATIVES FOR DEMOCRATIZING LIFE SCIENCE TECHNOLOGIES AND PROMOTING ACCESS TO HEALTHCARE
- ETHICAL CHALLENGES IN LIFE SCIENCES
- Prix Galien International Awards Ceremony
1. Sep 17, 2021 @ Thomas Jefferson Univ
Artificial Intelligence
in Radiation Oncology
Wookjin Choi, PhD
Assistant Professor of Computer Science
Virginia State University
wchoi@vsu.edu
2. Acknowledgements
Memorial Sloan Kettering Cancer Center
• Wei Lu PhD
• Sadegh Riyahi, PhD
• Jung Hun Oh, PhD
• Saad Nadeem, PhD
• Joseph O. Deasy, PhD
• Andreas Rimner, MD
• Prasad Adusumilli, MD
• Chia-ju Liu, MD
• Wolfgang Weber, MD
Stony Brook University
• Allen Tannenbaum, PhD
University of Virginia School of Medicine
• Jeffrey Siebers, PhD
• Victor Gabriel Leandro Alves, PhD
• Hamidreza Nourzadeh, PhD
• Eric Aliotta, PhD
University of Maryland School of Medicine
• Howard Zhang, PhD
• Wengen Chen, MD, PhD
• Charles White, MD
• Seth Kligerman, MD
• Shan Tan, PhD
• Jiahui Wang, PhD
2
NIH/NCI Grant R01 CA222216, R01 CA172638 and NIH/NCI Cancer Center Support Grant P30 CA008748
The ESTRO Falcon project team, Scott Kaylor of EduCase, Benjamin Nelms of Proknow for the multi-
delineator contour data presented in this work
3. AI in Radiation Oncology
3
Huynh et al. Nat Rev Clin Oncol 2020
4. 4
Netherton et al. Oncology 2021
Hype cycle for three major innovations
in radiation oncology
Automatable tasks in radiation oncology
for the modern clinic
5. Outline
Radiomics - Decision Support Tools
• Lung Cancer Screening
• Tumor Response Prediction and Evaluation
• Aggressive Lung ADC subtype prediction
• Multimodal data: Pathology, Multiomics, etc.
Auto Delineation and Variability Analysis
• Delineation Variability Quantification
• Dosimetric Consequences of Variabilities
• OARNet, Probabilistic U-Net
5
6. Radiomics
6
Controllable Feature Analysis
More Interpretable
Lambin, et al. Eur J Cancer 2012
Aerts et al., Nature Communications, 2014
7. Radiomics Framework
7
Image
Registration
• Multi-level rigid
• Deformable
• Pre/Post-CT
• MSE, MI
Tumor
Segmentation
• Adaptive region growing
• Level set
• Grow cut
• Morphology filter
• Multi-modality
image segmentation
Feature
Extraction
• Intensity distribution
• Spatial variations
(texture)
• Geometric properties
• Jacobian feature
from DVF
• Feature selection
Predictive
Model
• ROC analyses
• Prediction models
• Validation
• Tumor response
• Recurrence
• Survival
Source codes: https://github.com/taznux/radiomics-tools
• Automated Workflow (Python)
- Integrate all the radiomics components
- 3D Slicer, ITK (C++), Matlab, R, and Python
- Scalable: support multicore & GPU computing
8. Radiomics Framework
8
Image
Registration
• Multi-level rigid
• Deformable
• Pre/Post-CT
• MSE, MI
Tumor
Segmentation
• Adaptive region growing
• Level set
• Grow cut
• Morphology filter
• Multi-modality
image segmentation
Feature
Extraction
• Intensity distribution
• Spatial variations
(texture)
• Geometric properties
• Jacobian feature
from DVF
• Feature selection
Predictive
Model
• ROC analyses
• Prediction models
• Validation
• Tumor response
• Recurrence
• Survival
Source codes: https://github.com/taznux/radiomics-tools
Deep Learning Model
• Automated Workflow (Python)
• Integrate all the radiomics components
• 3D Slicer, ITK (C++), Matlab, R, and Python
• Scalable: support multicore & GPU computing
9. Radiomics Framework
9
Image
Registration
• Multi-level rigid
• Deformable
• Pre/Post-CT
• MSE, MI
Tumor
Segmentation
• Adaptive region growing
• Level set
• Grow cut
• Morphology filter
• Multi-modality
image segmentation
Feature
Extraction
• Intensity distribution
• Spatial variations
(texture)
• Geometric properties
• Jacobian feature
from DVF
• Feature selection
Predictive
Model
• ROC analyses
• Prediction models
• Validation
• Tumor response
• Recurrence
• Survival
Source codes: https://github.com/taznux/radiomics-tools
Deep Learning Model
• Automated Workflow (Python)
• Integrate all the radiomics components
• 3D Slicer, ITK (C++), Matlab, R, and Python
• Scalable: support multicore & GPU computing
10. Radiomics Framework
10
Image
Registration
• Multi-level rigid
• Deformable
• Pre/Post-CT
• MSE, MI
Tumor
Segmentation
• Adaptive region growing
• Level set
• Grow cut
• Morphology filter
• Multi-modality
image segmentation
Feature
Extraction
• Intensity distribution
• Spatial variations
(texture)
• Geometric properties
• Jacobian feature
from DVF
• Feature selection
Predictive
Model
• ROC analyses
• Prediction models
• Validation
• Tumor response
• Recurrence
• Survival
Source codes: https://github.com/taznux/radiomics-tools
Deep Learning Model
• Automated Workflow (Python)
• Integrate all the radiomics components
• 3D Slicer, ITK (C++), Matlab, R, and Python
• Scalable: support multicore & GPU computing
11. Radiomics Framework
11
Image
Registration
• Multi-level rigid
• Deformable
• Pre/Post-CT
• MSE, MI
Tumor
Segmentation
• Adaptive region growing
• Level set
• Grow cut
• Morphology filter
• Multi-modality
image segmentation
Feature
Extraction
• Intensity distribution
• Spatial variations
(texture)
• Geometric properties
• Jacobian feature
from DVF
• Feature selection
Predictive
Model
• ROC analyses
• Prediction models
• Validation
• Tumor response
• Recurrence
• Survival
Source codes: https://github.com/taznux/radiomics-tools
Deep Learning Model
• Automated Workflow (Python)
• Integrate all the radiomics components
• 3D Slicer, ITK (C++), Matlab, R, and Python
• Scalable: support multicore & GPU computing
13. Lung Cancer Screening
13
Early detection of lung cancer by LDCT can reduce mortality
Known features correlated with PN malignancy
Size, growth rate (Lung-RADS)
Calcification, enhancement, solidity → texture features
Boundary margins (spiculation, lobulation), attachment → shape and
appearance features
Malignant nodules Benign nodules
Size Total Malignancy
< 4mm 2038 0%
4-7 mm 1034 1%
8-20 mm 268 15%
> 20 mm 16 75%
14. ACR Lung-RADS
Category Baseline Screening Malignancy
1 No PNs; PNs with calcification
Negative
<1% chance of malignancy
2
Solid/part-solid: <6 mm
GGN: <20 mm
Benign appearance
<1% chance of malignancy
3
Solid: ≥6 to <8 mm
Part-solid: ≥6 mm with solid component <6 mm
GGN: ≥20 mm
Probably benign
1-2% chance of malignancy
4A
Solid: ≥8 to <15 mm
Part-solid: ≥8 mm with solid component ≥6 and <8 mm
Suspicious
5-15% chance of malignancy
4B
Solid: ≥15 mm
Part-solid: Solid component ≥8 mm
>15% chance of malignancy
4X
Category 3 or 4 PNs with suspicious features (e.g. enlarged lymph
nodes) or suspicious imaging findings (e.g. spiculation)
>15% chance of malignancy
14
ACR: American College of Radiology
Lung-RADS: Lung CT Screening Reporting and Data System
15. Lung Cancer Screening (Methodology)
• TCIA LIDC-IDRI public data set (n=1,010)
• Multi-institutional data
• 72 cases evaluated (31 benign and 41 malignant cases)
• Consensus contour
15
GLCM GLRM
Texture features Intensity features
2D
Shape features
3D
16. Lung Cancer Screening (SVM-LASSO Model )
16
SVM classification
Distinctive feature identification
Malignant?
Predicted malignancy
Feature extraction
Yes
10x10-fold
CV
10-fold
CV
LASSO feature selection
• Size (BB_AP) : Highly correlated with the axial longest diameter
and its perpendicular diameter (r = 0.96, larger – more
malignant)
• Texture (SD_IDM) : Tumor heterogeneity (smaller – more
malignant)
17. Lung Screening (Results: Comparison)
Sensitivity Specificity Accuracy AUC
Lung-RADS
Clinical guideline
73.3% 70.4% 72.2% 0.74
Hawkins et al. (2016)
Radiomics – 23 features
51.7 % 92.9% 80.0% 0.83
Ma et al. (2016)
Radiomics – 583 features
80.0% 85.5% 82.7%
Buty et al. (2016)
DL – 400 SH and 4096 AlexNet features
82.4%
Kumar et al. (2015)
DL: 5000 features
79.1% 76.1% 77.5%
Proposed
Radiomics: two features (Size and Texture)
87.2% 81.2% 84.6% 0.89
17
DL: Deep Learning, SH: Spherical Harmonics
Choi et al., Medical Physics, 2018.
18. ACR Lung-RADS
Category Baseline Screening Malignancy
1 No PNs; PNs with calcification
Negative
<1% chance of malignancy
2
Solid/part-solid: <6 mm
GGN: <20 mm
Benign appearance
<1% chance of malignancy
3
Solid: ≥6 to <8 mm
Part-solid: ≥6 mm with solid component <6 mm
GGN: ≥20 mm
Probably benign
1-2% chance of malignancy
4A
Solid: ≥8 to <15 mm
Part-solid: ≥8 mm with solid component ≥6 and <8 mm
Suspicious
5-15% chance of malignancy
4B
Solid: ≥15 mm
Part-solid: Solid component ≥8 mm
>15% chance of malignancy
4X
Category 3 or 4 PNs with suspicious features (e.g. enlarged lymph
nodes) or suspicious imaging findings (e.g. spiculation)
>15% chance of malignancy
18
ACR: American College of Radiology
Lung-RADS: Lung CT Screening Reporting and Data System
19. Spiculation Quantification (Motivation)
• Blind Radiomics
• Semantic Features
• Semi-automatic Segmentation
- GrowCut and LevelSet
19
Radiologists spiculation score (RS) for different pulmonary nodules
1 2 3 4 5
Choi et al. in CMPB 2021
23. Progression-free survival Prediction
after SBRT for early-stage NSCLC
23
Thor, Choi et al. ASTRO 2020
• 412 patients treated between 2006 and 2017
• PETs and CTs within three months prior to SBRT start.
• The median prescription dose was 50Gy in 5 fractions.
24. Progression-free survival Prediction (Results)
• PET entropy, CT number of peaks,
CT major axis, and gender.
• The most frequently selected model
included PET entropy and CT
number of peaks
- The c-index in the validation subset
was 0.77
- The prediction-stratified survival
indicated a clear separation between
the observed HR and LR
- e.g. a PFS of 60% was observed at 12
months in HR vs. 22 months in LR.
24
Thor, Choi et al. ASTRO 2020
25. Local tumor morphological changes
25
Jacobian Map
- Jacobian matrix: calculates rate of displacement change in each direction.
- Determinant indicates volumetric ratio of shrinkage/expansion.
𝐷𝑒𝑡 𝐽 =
𝐷𝑒𝑡 𝐽 > 1 volume expansion
𝐷𝑒𝑡 𝐽 = 1 no volume change
𝐷𝑒𝑡 𝐽 < 1 volume shrinkage
𝐷𝑒𝑡 𝐽 = 1.2 = 20% expansion
𝐷𝑒𝑡 𝐽 = 0.8 = 20% shrinkage (-20%)
Riyahi, Choi et al., PMB 2018
27. Local tumor morphological changes (Results)
Features P-value AUC Correlation to responders
Minimum Jacobian 0.009 0.98 -0.79
Median Jacobian 0.046 0.95 -0.72
The P-value, AUC and correlation to responders for all significant features in univariate analysis
27
Riyahi, Choi et al., PMB 2018 SVM-LASSO: AUC 0.91
28. Aggressive Lung ADC Subtype Prediction (Motivation)
28
CT
MIP
PET/CT
Soild
CT PET/CT
Five classifications of lung ADC Travis et
al. JTO 2011
Solid and MIP components: poor surgery/SBRT prognosis factor
Benefit from lobectomy rather than limited resection
Core biopsy (Leeman et al. IJROBP 2017)
Minimally invasive, not routinely performed, sampling error (about 60%
agreement with pathology)
Preoperative diagnostic CT and FDG PET/CT radiomics
Non-invasive and routinely performed
29. Aggressive Lung ADC Subtype Prediction (Method & Results)
• Retrospectively enrolled 120 patients
- Stage I lung ADC, ≤2cm
- Preoperative diagnostic CT and FDG PET/CT
• Histopathologic endpoint
- Aggressiveness (Solid : 18 cases, MIP : 5 cases)
• 206 radiomic features & 14 clinical parameters
• SVM-LASSO model
29
Performance of the SVM-LASSO model to predict aggressive lung ADC
Choi et al. Manuscript under review
Box plots of SUVmax (FDR q=0.004) and PET Mean of
Cluster Shade (q=0.002)
Feature Sensitivity Specificity PPV NPV Accuracy AUC
Conventional SUVmax 57.8±4.6% 78.5±1.4% 39.2±2.3% 88.6±1.1% 74.5±1.4% 0.64±0.01
SVM-LASSO
PET Mean of Cluster
Shade
67.4±3.1% 86.0±1.1% 53.7±2.1% 91.7±1.0% 82.4±1.0% 0.78±0.01
p-value SUVmax vs. SVM-LASSO 0.002 1e-5 7e-8 3e-5 5e-8 0.03
30. Unsupervised Learning of Deep Learned Features
from Breast Cancer Images
30
Lee, Choi et al. IEEE BIBE 2020
32. PathCNN: interpretable convolutional neural networks
for survival prediction and pathway analysis applied to glioblastoma
32
Oh, Choi et al. Bioinformatics 2021, joint first author Source code: https://github.com/mskspi/PathCNN.
• CNNs have achieved great success
• A lack of interpretability remains
a key barrier
• Moreover, because biological array
data are generally represented in a
non-grid structured format
• PathCNN
An interpretable CNN model on
integrated multi-omics data using
a newly defined pathway image.
33. PathCNN: interpretable CNNs (results)
33
Cancer PathCNN Logistic
regression SVM with RBF Neural network MiNet
GBM 0.755 ± 0.009 0.668 ± 0.039 0.685 ± 0.037 0.692 ± 0.030 0.690 ± 0.032
LGG 0.877 ± 0.007 0.816 ± 0.036 0.884 ± 0.017 0.791 ± 0.031 0.854 ± 0.027
LUAD 0.637 ± 0.014 0.581 ± 0.028 0.624 ± 0.034 0.573 ± 0.031 0.597 ± 0.042
KIRC 0.709 ± 0.009 0.654 ± 0.034 0.684 ± 0.027 0.702 ± 0.028 0.659 ± 0.030
Comparison of predictive performance with benchmark methods in terms of the area
under the curve (AUC: mean ± standard deviation) over 30 iterations of the 5-fold
cross validation
Note: AUCs for PathCNN were obtained with three principal components. Bold = Highest AUC for each dataset.
SVM, support vector machine; RBF, radial basis function; MiNet, Multi-omics Integrative Net; GBM, glioblastoma
multiforme; LGG, low-grade glioma; LUAD, lung adenocarcinoma; KIRC, kidney cancer.
Oh, Choi et al. Bioinformatics 2021, joint first author Source code: https://github.com/mskspi/PathCNN.
34. Outline
Radiomics - Decision Support Tools
• Lung Cancer Screening
• Tumor Response Prediction and Evaluation
• Aggressive Lung ADC subtype prediction
• Multimodal data: Pathology, Multiomics, etc.
Auto Delineation and Variability Analysis
• Delineation Variability Quantification
• Dosimetric Consequences of Variabilities
• OARNet, Probabilistic U-Net
34
35. Delineation Variability Quantification and Simulation
A framework for radiation therapy variability analysis
35
RT plan
Structure Set
CT Image
Dose Distribution
Structure Sets
DV simulation
ASSD
GrowCut
RW
Other delineators
SV analysis
DV analysis
Geometric
Dosimetric
Variability analysis
Human DV
Simulated
DV
Consensus SS
OARNet
Choi et al., AAPM, 2019.
36. Delineation Variability Quantification and
Simulation
• ESTRO Falcon contour workshop (EduCase)
- A HNC case, Larynx, 70 Gy and 35 fractions
- 14 independent manually delineated (MD) OAR structure sets (SS)
- BrainStem, Esophagus, OralCavity, Parotid_L, Parotid_R, SpinalCord, and Thyroid
• Consensus MD SS
- The simultaneous truth and performance level estimation (STAPLE)
36
Choi, Nourzadeh et al., AAPM, 2019.
37. Delineation Variability Quantification and
Simulation (Methods)
•Geometric analysis
- Similarity: Dice coefficient (Volumetric, Surface)
- Distance: Hausdorff distance (HD), Actual Average Surface
Distance (AASD)
- Reference: STAPLE SS
•Dosimetric analysis
- Single dose distribution planned from a human SS
- DVH confidence bands (90%tile)
- 𝐷mean, 𝐷max, 𝐷min, 𝐷50
37
Choi, Nourzadeh et al., AAPM, 2019.
38. Delineation Variability Quantification and Simulation (Results)
• DVH variability not predicted by geometric measures
• Large human variability
38
100%
50%
0%
100%
50%
0%
Human ASSD GrowCut RW
Right
Parotid
Left
Parotid
Choi, Nourzadeh et al., AAPM, 2019.
47. A Probabilistic U-Net for Segmentation of Ambiguous Images
Kohl et al. NeurIPS 2018 47
48. Segmentations on different Variability levels (middle 5) and their occupancy map
• Implemented the model using PyTorch
• Model trained using TCIA LIDC dataset (about 2000 nodules with up to 4 radiologists delineations)
• Titan Xp, 12GB (1 week for training)
• Unstable to train, 2D segmentation, tumor
A Probabilistic U-Net (Results)
48
Variability
Low High
49. A Probabilistic U-Net for Segmentation of Ambiguous Images
Wasserstein distance?
2D → 2.5D → 3D 49
50. Summary
Radiomics - Decision Support Tools
• Lung Cancer Screening
• Tumor Response Prediction and Evaluation
• Aggressive Lung ADC subtype prediction
• Multimodal data: Pathology, Multiomics, etc.
Auto Delineation and Variability Analysis
• Delineation Variability Quantification
• Dosimetric Consequences of Variabilities
• OARNet, Probabilistic U-Net
50
51. Short-term Future Works
• Human-Variability aware auto-delineation
• Variability quantification and simulation using generative models
• OARNet + Probabilistic U-Net → Probabilistic OARNet
• Develop interpretable radiomic features
• Improve spiculation quantification
• Multi-institution validation
• Integrate the radiomics framework into TPS
• Eclipse (C#), MIM (Python), RayStation (Python)
51
52. Long-term Future Works
• Comprehensive Framework for Cancer Imaging
• Multi-modal imaging
• Response prediction and evaluation (Pre, Mid, and Post)
• Longitudinal analysis of tumor change
• Shape analysis (e.g. Spiculation)
• Deep learning models
• Automation of Clinical Workflow
• Big Data Analytics: EMR, PACS, ROIS, Genomics, etc.
• Provide an informatics platform for comprehensive cancer therapy
52
53. Selected Publications
1. Jung Hun Oh*, Wookjin Choi* et al., “PathCNN: interpretable convolutional neural networks for survival prediction and
pathway analysis applied to glioblastoma”, Bioinformatics, 2021, *joint first author
2. Wookjin Choi et al., “ Reproducible and Interpretable Spiculation Quantification for Lung Cancer Screening”, Computer
Methods and Programs in Biomedicine”, 2021
3. Noemi Garau, Wookjin Choi, et al., “ External validation of radiomics‐based predictive models in low‐dose CT screening
for early lung cancer diagnosis”, Medical Physics, 2020
4. Jiahui Wang, Wookjin Choi et al., “Prediction of anal cancer recurrence after chemoradiotherapy using quantitative
image features extracted from serial 18F-FDG PET/CT”, Frontiers in oncology, 2019
5. Wookjin Choi et al., “Radiomics analysis of pulmonary nodules in low-dose CT for early detection of lung cancer”,
Medical Physics, 2018
6. Sadegh Riyahi, Wookjin Choi, et al., “Quantifying local tumor morphological changes with Jacobian map for prediction of
pathologic tumor response to chemo-radiotherapy in locally advanced esophageal cancer”, Physics in Medicine and
Biology, 2018
7. Shan Tan, Laquan Li, Wookjin Choi, et al., “Adaptive region-growing with maximum curvature strategy for tumor
segmentation in 18F-FDG PET”, Physics in Medicine and Biology, 2017
8. Wookjin Choi et al., “Individually Optimized Contrast-Enhanced 4D-CT for Radiotherapy Simulation in Pancreatic Ductal
Adenocarcinoma”, Medical Physics, 2016
9. Wookjin Choi, Tae-Sun Choi, “Automated Pulmonary Nodule Detection based on Three-dimensional Shape-based
Feature Descriptor”, Computer Methods and Programs in Biomedicine, 2014
53
Complete list of publications: https://scholar.google.com/citations?user=iHgsGLUAAAAJ
54. 54
Thank You!
Q & A
https://qradiomics.wordpress.com
E-mail: wchoi@vsu.edu
55. Spiculation Quantification: Height, Area Distortion
• Area distortion better than solid angle for non-conic spicules
• Height is medial axis length, can be perpendicular distance
• Width is measured at base, can be FWHM
𝑠1 =
𝑖 mean 𝜖𝑝 𝑖 ∗ ℎ𝑝 𝑖
𝑖 ℎ𝑝 𝑖
𝑠2 =
𝑖 min 𝜖𝑝 𝑖 ∗ ℎ𝑝 𝑖
𝑖 ℎ𝑝 𝑖
55
58. Delineation Variability Simulation (Methods)
• DV Simulation using auto-delineation (AD) methods (σ=2, 5, 10 mm)
• Average surface of standard deviation (ASSD): random perturbation
• GrowCut: cellular automata region growing
• Random walker (RW): probabilistic segmentation
58
Background 0
Foreground 1
Initial Binary Mask
Gaussian-Smoothed Mask
Gaussian Noises-Added Mask
Intensity
Spatial location
Inside
Outside
σ = 2mm σ = 5mm σ = 8mm σ = 10mm
Choi et al., AAPM, 2019.
59. OARNet comparisons
59
(a) Dice similarity coefficient and (b) Hausdorff comparison for the alternative delineation
methods. The points in the graphs are mean values and bars show the 95% confidence intervals.
60. 60
A matrix of adjusted P-values.The row represents the 146 KEGG pathways ordered on pathway images.
The columns represent the first two principal components of each omics type.The red color indicates key
pathways with adjusted P-values < 0.001
Editor's Notes
Thank you for coming today! It’s an honor to have the opportunity to share my research here TJU.
I’m going to talk about -
I would like to thank everyone who has helped me in the projects
a general overview of the radiation therapy workflow with brief descriptions of expected applications of artificial intelligence (AI) at each step.
The workflow begins with the decision to treat the patient with radiation therapy,
followed by a simulation appointment during which medical images are acquired for treatment planning.
Subsequently, the patient-specific treatment plan is created,
and then the plan is subjected to approval, review and quality assurance (QA) measures prior to delivery of radiation to the patient.
The patient then receives follow-up care.
AI has the potential to improve radiation therapy for patients with cancer by increasing efficiency for the staff involved, improving the quality of treatments, and providing additional clinical information and predictions of treatment response to assist and improve clinical decision-making.
(triangle: Monte Carlo; square: Inverse optimization/IMRT; circle: deep learning-based contouring). The curve depicts expectations by the target audience (those in radiation oncology and medical physics) as a function of time. Yellow, magenta, cyan, green, and blue portions of the curve denote “innovation trigger,” “peak of inflated expectations,” “trough of disillusionment,” “slope of enlightenment,” and “productivity plateau” regions, respectively.
Automatable tasks in radiation oncology for the modern clinic. The extent to which each skill set is used or task is performed in this figure is not indicated and may be dependent on each clinical practice. In order to group essential tasks performed during the treatment planning process, “Physical,” “Knowledge,” and “Social” skill domains were created and are indicated by green, magenta, and blue ellipses, respectively. Skills or tasks are indicated by circles within each colored domain and may be shared between domains. Based on works cited in this review, tasks which may be automated are within the “Automatable” domain.
How to generalize it
A large number of image features from medical images
additional information that has prognostic value
I open sample automated workflow and essential components to public
I open sample automated workflow and essential components to public
I open sample automated workflow and essential components to public
I open sample automated workflow and essential components to public
I open sample automated workflow and essential components to public
I open sample automated workflow and essential components to public
Frequent use of LDCT increased number of indeterminate PNs
Prediction of PN malignancy is important
The Lung Imaging Reporting and Data System (Lung-RADS) was developed by the American College of Radiology (ACR) to standardize the screening of lung cancer on CT images.
As shown in the Table, the Lung-RADS categorization is mainly based on PN size (the average of the longest and shortest diameters on axial slice)
with some consideration to calcification, appearance type (solid, part-solid, and non-solid or ground glass nodule/GGN), and additional suspicious features.
We also performed Lung-RADS categorization based on the PN contour and the physician’s annotations.
To match the original LIDC-IDRI diagnosis, categories 3 and lower are labeled as benign and category 4 (4A, 4B, and 4X) as malignant.
79 LDCT scans: 36 benign and 43 malignant cases, 7 missing contours
We performed Lung-RADS categorization based on the PN contour and the physician’s annotations.
Having diagnosis data 157
Primary cancer 43 -> 41 biopsy-proven, progression
Benign 36 -> 31 biopsy-proven, 2yrs of stable PN, progression
Metastatic cancer or unknown 78
To increase interpretability, need concise model with minimum number of features
The proposed method showed comparable or better accuracy than others,
Better than deep learning with two features
The Lung Imaging Reporting and Data System (Lung-RADS) was developed by the American College of Radiology (ACR) to standardize the screening of lung cancer on CT images.
As shown in the Table, the Lung-RADS categorization is mainly based on PN size (the average of the longest and shortest diameters on axial slice)
with some consideration to calcification, appearance type (solid, part-solid, and non-solid or ground glass nodule/GGN), and additional suspicious features.
We also performed Lung-RADS categorization based on the PN contour and the physician’s annotations.
To match the original LIDC-IDRI diagnosis, categories 3 and lower are labeled as benign and category 4 (4A, 4B, and 4X) as malignant.
Spiculations are spikes on the surface of PN and are important predictors of malignancy in lung cancer