PMID- 36110933 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20231115 IS - 2234-943X (Print) IS - 2234-943X (Electronic) IS - 2234-943X (Linking) VI - 12 DP - 2022 TI - Auto-segmentation for total marrow irradiation. PG - 970425 LID - 10.3389/fonc.2022.970425 [doi] LID - 970425 AB - PURPOSE: To evaluate the accuracy and efficiency of Artificial-Intelligence (AI) segmentation in Total Marrow Irradiation (TMI) including contours throughout the head and neck (H&N), thorax, abdomen, and pelvis. METHODS: An AI segmentation software was clinically introduced for total body contouring in TMI including 27 organs at risk (OARs) and 4 planning target volumes (PTVs). This work compares the clinically utilized contours to the AI-TMI contours for 21 patients. Structure and image dicom data was used to generate comparisons including volumetric, spatial, and dosimetric variations between the AI- and human-edited contour sets. Conventional volume and surface measures including the Sorensen-Dice coefficient (Dice) and the 95(th)% Hausdorff Distance (HD95) were used, and novel efficiency metrics were introduced. The clinical efficiency gains were estimated by the percentage of the AI-contour-surface within 1mm of the clinical contour surface. An unedited AI-contour has an efficiency gain=100%, an AI-contour with 70% of its surface<1mm from a clinical contour has an efficiency gain of 70%. The dosimetric deviations were estimated from the clinical dose distribution to compute the dose volume histogram (DVH) for all structures. RESULTS: A total of 467 contours were compared in the 21 patients. In PTVs, contour surfaces deviated by >1mm in 38.6% +/- 23.1% of structures, an average efficiency gain of 61.4%. Deviations >5mm were detected in 12.0% +/- 21.3% of the PTV contours. In OARs, deviations >1mm were detected in 24.4% +/- 27.1% of the structure surfaces and >5mm in 7.2% +/- 18.0%; an average clinical efficiency gain of 75.6%. In H&N OARs, efficiency gains ranged from 42% in optic chiasm to 100% in eyes (unedited in all cases). In thorax, average efficiency gains were >80% in spinal cord, heart, and both lungs. Efficiency gains ranged from 60-70% in spleen, stomach, rectum, and bowel and 75-84% in liver, kidney, and bladder. DVH differences exceeded 0.05 in 109/467 curves at any dose level. The most common 5%-DVH variations were in esophagus (86%), rectum (48%), and PTVs (22%). CONCLUSIONS: AI auto-segmentation software offers a powerful solution for enhanced efficiency in TMI treatment planning. Whole body segmentation including PTVs and normal organs was successful based on spatial and dosimetric comparison. CI - Copyright (c) 2022 Watkins, Qing, Han, Hui and Liu. FAU - Watkins, William Tyler AU - Watkins WT AD - Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, United States. FAU - Qing, Kun AU - Qing K AD - Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, United States. FAU - Han, Chunhui AU - Han C AD - Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, United States. FAU - Hui, Susanta AU - Hui S AD - Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, United States. FAU - Liu, An AU - Liu A AD - Department of Radiation Oncology, City of Hope National Medical Center, Duarte, CA, United States. LA - eng GR - R01 CA154491/CA/NCI NIH HHS/United States PT - Journal Article DEP - 20220830 PL - Switzerland TA - Front Oncol JT - Frontiers in oncology JID - 101568867 PMC - PMC9468379 OTO - NOTNLM OT - artificial intelligence OT - auto-contouring OT - auto-segmentation OT - total marrow irradiation OT - total marrow lymphoid irradiation COIS- AL, KQ, CH, and TW have a research collaboration with Medical Mind, Inc. The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2022/09/17 06:00 MHDA- 2022/09/17 06:01 PMCR- 2022/01/01 CRDT- 2022/09/16 02:40 PHST- 2022/06/15 00:00 [received] PHST- 2022/07/21 00:00 [accepted] PHST- 2022/09/16 02:40 [entrez] PHST- 2022/09/17 06:00 [pubmed] PHST- 2022/09/17 06:01 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fonc.2022.970425 [doi] PST - epublish SO - Front Oncol. 2022 Aug 30;12:970425. doi: 10.3389/fonc.2022.970425. eCollection 2022.