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1.
Comput Biol Med ; 177: 108675, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38820779

ABSTRACT

BACKGROUND: The different tumor appearance of head and neck cancer across imaging modalities, scanners, and acquisition parameters accounts for the highly subjective nature of the manual tumor segmentation task. The variability of the manual contours is one of the causes of the lack of generalizability and the suboptimal performance of deep learning (DL) based tumor auto-segmentation models. Therefore, a DL-based method was developed that outputs predicted tumor probabilities for each PET-CT voxel in the form of a probability map instead of one fixed contour. The aim of this study was to show that DL-generated probability maps for tumor segmentation are clinically relevant, intuitive, and a more suitable solution to assist radiation oncologists in gross tumor volume segmentation on PET-CT images of head and neck cancer patients. METHOD: A graphical user interface (GUI) was designed, and a prototype was developed to allow the user to interact with tumor probability maps. Furthermore, a user study was conducted where nine experts in tumor delineation interacted with the interface prototype and its functionality. The participants' experience was assessed qualitatively and quantitatively. RESULTS: The interviews with radiation oncologists revealed their preference for using a rainbow colormap to visualize tumor probability maps during contouring, which they found intuitive. They also appreciated the slider feature, which facilitated interaction by allowing the selection of threshold values to create single contours for editing and use as a starting point. Feedback on the prototype highlighted its excellent usability and positive integration into clinical workflows. CONCLUSIONS: This study shows that DL-generated tumor probability maps are explainable, transparent, intuitive and a better alternative to the single output of tumor segmentation models.


Subject(s)
Deep Learning , Head and Neck Neoplasms , Humans , Head and Neck Neoplasms/diagnostic imaging , User-Computer Interface , Positron Emission Tomography Computed Tomography/methods
2.
Radiother Oncol ; 196: 110319, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38702014

ABSTRACT

BACKGROUND AND PURPOSE: Recently, a comprehensive xerostomia prediction model was published, based on baseline xerostomia, mean dose to parotid glands (PG) and submandibular glands (SMG). Previously, PET imaging biomarkers (IBMs) of PG were shown to improve xerostomia prediction. Therefore, this study aimed to explore the potential improvement of the additional PET-IBMs from both PG and SMG to the recent comprehensive xerostomia prediction model (i.e., the reference model). MATERIALS AND METHODS: Totally, 540 head and neck cancer patients were split into training and validation cohorts. PET-IBMs from the PG and SMG, were selected using bootstrapped forward selection based on the reference model. The IBMs from both the PG and SMG with the highest selection frequency were added to the reference model, resulting in a PG-IBM model and a SMG-IBM model which were combined into a composite model. Model performance was assessed using the area under the curve (AUC). Likelihood ratio test compared the predictive performance between the reference model and models including IBMs. RESULTS: The final selected PET-IBMs were 90th percentile of the PG SUV and total energy of the SMG SUV. The additional two PET-IBMs in the composite model improved the predictive performance of the reference model significantly. The AUC of the reference model and the composite model were 0.67 and 0.69 in the training cohort, and 0.71 and 0.73 in the validation cohort, respectively. CONCLUSION: The composite model including two additional PET-IBMs from PG and SMG improved the predictive performance of the reference xerostomia model significantly, facilitating a more personalized prediction approach.


Subject(s)
Fluorodeoxyglucose F18 , Head and Neck Neoplasms , Positron-Emission Tomography , Xerostomia , Humans , Head and Neck Neoplasms/diagnostic imaging , Female , Male , Middle Aged , Xerostomia/diagnostic imaging , Xerostomia/etiology , Positron-Emission Tomography/methods , Radiopharmaceuticals , Aged , Adult , Submandibular Gland/diagnostic imaging , Parotid Gland/diagnostic imaging , Salivary Glands/diagnostic imaging
4.
Radiother Oncol ; 180: 109458, 2023 03.
Article in English | MEDLINE | ID: mdl-36608769

ABSTRACT

BACKGROUND AND PURPOSE: Previously, PET image biomarkers (PET-IBMs) - the 90th percentile standardized uptake value (P90-SUV) and the Mean SUV (Mean-SUV) of the contralateral parotid gland (cPG) - were identified as predictors for late-xerostomia following head and neck cancer (HNC) radiotherapy. The aim of the current study was to assess in an independent validation cohort whether these pre-treatment PET-IBM can improve late-xerostomia prediction compared to the prediction with baseline xerostomia and mean cPG dose alone. MATERIALS AND METHODS: The prediction endpoint was patient-rated moderate-to-severe xerostomia at 12 months after radiotherapy. The PET-IBMs were extracted from pre-treatment 18 F-FDG PET images. The performance of the model (base model) with baseline xerostomia and mean cPG dose alone and models with additionally P90-SUV or Mean-SUV were tested in the current independent validation cohort. Specifically, model discrimination (area under the curve: AUC) and calibration (calibration plot) were evaluated. RESULTS: The current validation cohort consisted of 137 patients of which 40% developed moderate-to-severe xerostomia at 12 months. Both the PET-P90 model (AUC:PET-P90 = 0.71) and the PET-Mean model (AUC: PET-Mean = 0.70) performed well in the current validation cohort. Moreover, their performance were improved compared to the base model (AUC:base model= 0.68). The calibration plots showed a good fit of the prediction to the actual rates for all tested models. CONCLUSION: PET-IBMs showed an improved prediction of late-xerostomia when added to the base model in this validation cohort. This contributed to the published hypothesis that PET-IBMs include individualized information and can serve as a pre-treatment risk factor for late-xerostomia.


Subject(s)
Head and Neck Neoplasms , Xerostomia , Humans , Fluorodeoxyglucose F18 , Xerostomia/diagnostic imaging , Xerostomia/etiology , Head and Neck Neoplasms/radiotherapy , Biomarkers , Parotid Gland , Positron-Emission Tomography
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