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Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy

AIMS: This study aimed to examine whether any significant differences existed in trial protocol compliance in target volumes (TV) and organs at risk (OARs) contouring amongst clinical oncologists specialised in lung cancer radiotherapy. MATERIALS/METHODS: Two lung radiotherapy trials that require al...

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Autores principales: Tsang, Yatman, Hoskin, Peter, Spezi, Emiliano, Landau, David, Lester, Jason, Miles, Elizabeth, Conibear, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033767/
https://www.ncbi.nlm.nih.gov/pubmed/32095541
http://dx.doi.org/10.1016/j.tipsro.2019.05.001
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author Tsang, Yatman
Hoskin, Peter
Spezi, Emiliano
Landau, David
Lester, Jason
Miles, Elizabeth
Conibear, John
author_facet Tsang, Yatman
Hoskin, Peter
Spezi, Emiliano
Landau, David
Lester, Jason
Miles, Elizabeth
Conibear, John
author_sort Tsang, Yatman
collection PubMed
description AIMS: This study aimed to examine whether any significant differences existed in trial protocol compliance in target volumes (TV) and organs at risk (OARs) contouring amongst clinical oncologists specialised in lung cancer radiotherapy. MATERIALS/METHODS: Two lung radiotherapy trials that require all prospective investigators to submit pre-trial outlining quality assurance (QA) benchmark cases were selected. The contours from the benchmark cases were compared against a set of reference contours which were defined by the trial management group (TMG). In order to quantify the degree of variation in TV and OARs contouring, the matching index (MI), Dice coefficient (DICE), Jaccard index (JI), Van‘t Riet Index and geographical miss index (GMI) were calculated. RESULTS: A total of 198 structures contoured by 21 clinicians were collected from the outlining benchmark cases. There were 40 clinical target volumes (CTV), 32 spinal cord, 36 oesophagus, 36 heart and 54 lungs volumes included in the study. Analysis of the pre-trial benchmark cases revealed statistically significant differences (p ≤ 0.05) in trial protocol compliances between clinical oncologists’ target volume and organs at risk contours. Our results demonstrated that the lung contours had the highest level of conformity, followed by heart, CTV, spinal cord and oesophagus respectively. CONCLUSIONS: This study showed that there was a statistically significant difference in trial protocol compliance for lung clinical oncologists’ TV and OARs contouring within the pre-trial QA benchmark cases. Trial protocol compliances of TV and OARs delineation can be identified through assessing outlining QA benchmark cases.
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spelling pubmed-70337672020-02-24 Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy Tsang, Yatman Hoskin, Peter Spezi, Emiliano Landau, David Lester, Jason Miles, Elizabeth Conibear, John Tech Innov Patient Support Radiat Oncol Research article AIMS: This study aimed to examine whether any significant differences existed in trial protocol compliance in target volumes (TV) and organs at risk (OARs) contouring amongst clinical oncologists specialised in lung cancer radiotherapy. MATERIALS/METHODS: Two lung radiotherapy trials that require all prospective investigators to submit pre-trial outlining quality assurance (QA) benchmark cases were selected. The contours from the benchmark cases were compared against a set of reference contours which were defined by the trial management group (TMG). In order to quantify the degree of variation in TV and OARs contouring, the matching index (MI), Dice coefficient (DICE), Jaccard index (JI), Van‘t Riet Index and geographical miss index (GMI) were calculated. RESULTS: A total of 198 structures contoured by 21 clinicians were collected from the outlining benchmark cases. There were 40 clinical target volumes (CTV), 32 spinal cord, 36 oesophagus, 36 heart and 54 lungs volumes included in the study. Analysis of the pre-trial benchmark cases revealed statistically significant differences (p ≤ 0.05) in trial protocol compliances between clinical oncologists’ target volume and organs at risk contours. Our results demonstrated that the lung contours had the highest level of conformity, followed by heart, CTV, spinal cord and oesophagus respectively. CONCLUSIONS: This study showed that there was a statistically significant difference in trial protocol compliance for lung clinical oncologists’ TV and OARs contouring within the pre-trial QA benchmark cases. Trial protocol compliances of TV and OARs delineation can be identified through assessing outlining QA benchmark cases. Elsevier 2019-06-22 /pmc/articles/PMC7033767/ /pubmed/32095541 http://dx.doi.org/10.1016/j.tipsro.2019.05.001 Text en Crown Copyright © 2019 Published by Elsevier B.V. on behalf of European Society for Radiotherapy & Oncology. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research article
Tsang, Yatman
Hoskin, Peter
Spezi, Emiliano
Landau, David
Lester, Jason
Miles, Elizabeth
Conibear, John
Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
title Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
title_full Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
title_fullStr Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
title_full_unstemmed Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
title_short Assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
title_sort assessment of contour variability in target volumes and organs at risk in lung cancer radiotherapy
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7033767/
https://www.ncbi.nlm.nih.gov/pubmed/32095541
http://dx.doi.org/10.1016/j.tipsro.2019.05.001
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