Literature DB >> 30836167

Deep Learning-Based Delineation of Head and Neck Organs at Risk: Geometric and Dosimetric Evaluation.

Ward van Rooij1, Max Dahele2, Hugo Ribeiro Brandao2, Alexander R Delaney2, Berend J Slotman2, Wilko F Verbakel2.   

Abstract

PURPOSE: Organ-at-risk (OAR) delineation is a key step in treatment planning but can be time consuming, resource intensive, subject to variability, and dependent on anatomical knowledge. We studied deep learning (DL) for automated delineation of multiple OARs; in addition to geometric evaluation, the dosimetric impact of using DL contours for treatment planning was investigated. METHODS AND MATERIALS: The following OARs were delineated with DL developed in-house: both submandibular and parotid glands, larynx, cricopharynx, pharyngeal constrictor muscle (PCM), upper esophageal sphincter, brain stem, oral cavity, and esophagus. DL contours were benchmarked against the manual delineation (MD) clinical contours using the Sørensen-Dice similarity coefficient. Automated knowledge-based treatment plans were used. The mean dose to the manually delineated OAR structures was reported for the MD and DL plans.
RESULTS: DL delineation of all OARs took <10 seconds per patient. For 7 of 11 OARs, the average Sørensen-Dice similarity coefficient was good (0.78-0.83). However, performance was lower for the esophagus (0.60), brainstem (0.64), PCM (0.68), and cricopharynx (0.73), often because of variations in MD. Although the average dose was statistically significantly higher in the DL plans for the inferior PCM (1.4 Gy) and esophagus (2.2 Gy), these average differences were not clinically significant. Dose to 28 of 209 (13.4%) and 7 of 209 (3.3%) OARs was >2 Gy higher and >2 Gy lower, respectively, in the DL plans.
CONCLUSIONS: DL-based segmentation for head and neck OARs is fast; for most organs and most patients, it performs sufficiently well for treatment-planning purposes. It has the potential to increase efficiency and facilitate online adaptive radiation therapy.
Copyright © 2019 Elsevier Inc. All rights reserved.

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Year:  2019        PMID: 30836167     DOI: 10.1016/j.ijrobp.2019.02.040

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  29 in total

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