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Dosimetric impact of adaptive proton therapy in head and neck cancer – A review

BACKGROUND: Intensity Modulated Proton Therapy (IMPT) in head and neck cancer (HNC) is susceptible to anatomical changes and patient set-up inaccuracies during the radiotherapy course, which can cause discrepancies between planned and delivered dose. The discrepancies can be counteracted by adaptive...

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Autores principales: Huiskes, Merle, Astreinidou, Eleftheria, Kong, Wens, Breedveld, Sebastiaan, Heijmen, Ben, Rasch, Coen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969246/
https://www.ncbi.nlm.nih.gov/pubmed/36860581
http://dx.doi.org/10.1016/j.ctro.2023.100598
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author Huiskes, Merle
Astreinidou, Eleftheria
Kong, Wens
Breedveld, Sebastiaan
Heijmen, Ben
Rasch, Coen
author_facet Huiskes, Merle
Astreinidou, Eleftheria
Kong, Wens
Breedveld, Sebastiaan
Heijmen, Ben
Rasch, Coen
author_sort Huiskes, Merle
collection PubMed
description BACKGROUND: Intensity Modulated Proton Therapy (IMPT) in head and neck cancer (HNC) is susceptible to anatomical changes and patient set-up inaccuracies during the radiotherapy course, which can cause discrepancies between planned and delivered dose. The discrepancies can be counteracted by adaptive replanning strategies. This article reviews the observed dosimetric impact of adaptive proton therapy (APT) and the timing to perform a plan adaptation in IMPT in HNC. METHODS: A literature search of articles published in PubMed/MEDLINE, EMBASE and Web of Science from January 2010 to March 2022 was performed. Among a total of 59 records assessed for possible eligibility, ten articles were included in this review. RESULTS: Included studies reported on target coverage deterioration in IMPT plans during the RT course, which was recovered with the application of an APT approach. All APT plans showed an average improved target coverage for the high- and low-dose targets as compared to the accumulated dose on the planned plans. Dose improvements up to 2.5 Gy (3.5 %) and up to 4.0 Gy (7.1 %) in the D98 of the high- and low dose targets were observed with APT. Doses to the organs at risk (OARs) remained equal or decreased slightly after APT was applied. In the included studies, APT was largely performed once, which resulted in the largest target coverage improvement, but eventual additional APT improved the target coverage further. There is no data showing what is the most appropriate timing for APT. CONCLUSION: APT during IMPT for HNC patients improves target coverage. The largest improvement in target coverage was found with a single adaptive intervention, and an eventual second or more frequent APT application improved the target coverage further. Doses to the OARs remained equal or decreased slightly after applying APT. The most optimal timing for APT is yet to be determined.
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spelling pubmed-99692462023-02-28 Dosimetric impact of adaptive proton therapy in head and neck cancer – A review Huiskes, Merle Astreinidou, Eleftheria Kong, Wens Breedveld, Sebastiaan Heijmen, Ben Rasch, Coen Clin Transl Radiat Oncol Review Article BACKGROUND: Intensity Modulated Proton Therapy (IMPT) in head and neck cancer (HNC) is susceptible to anatomical changes and patient set-up inaccuracies during the radiotherapy course, which can cause discrepancies between planned and delivered dose. The discrepancies can be counteracted by adaptive replanning strategies. This article reviews the observed dosimetric impact of adaptive proton therapy (APT) and the timing to perform a plan adaptation in IMPT in HNC. METHODS: A literature search of articles published in PubMed/MEDLINE, EMBASE and Web of Science from January 2010 to March 2022 was performed. Among a total of 59 records assessed for possible eligibility, ten articles were included in this review. RESULTS: Included studies reported on target coverage deterioration in IMPT plans during the RT course, which was recovered with the application of an APT approach. All APT plans showed an average improved target coverage for the high- and low-dose targets as compared to the accumulated dose on the planned plans. Dose improvements up to 2.5 Gy (3.5 %) and up to 4.0 Gy (7.1 %) in the D98 of the high- and low dose targets were observed with APT. Doses to the organs at risk (OARs) remained equal or decreased slightly after APT was applied. In the included studies, APT was largely performed once, which resulted in the largest target coverage improvement, but eventual additional APT improved the target coverage further. There is no data showing what is the most appropriate timing for APT. CONCLUSION: APT during IMPT for HNC patients improves target coverage. The largest improvement in target coverage was found with a single adaptive intervention, and an eventual second or more frequent APT application improved the target coverage further. Doses to the OARs remained equal or decreased slightly after applying APT. The most optimal timing for APT is yet to be determined. Elsevier 2023-02-16 /pmc/articles/PMC9969246/ /pubmed/36860581 http://dx.doi.org/10.1016/j.ctro.2023.100598 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review Article
Huiskes, Merle
Astreinidou, Eleftheria
Kong, Wens
Breedveld, Sebastiaan
Heijmen, Ben
Rasch, Coen
Dosimetric impact of adaptive proton therapy in head and neck cancer – A review
title Dosimetric impact of adaptive proton therapy in head and neck cancer – A review
title_full Dosimetric impact of adaptive proton therapy in head and neck cancer – A review
title_fullStr Dosimetric impact of adaptive proton therapy in head and neck cancer – A review
title_full_unstemmed Dosimetric impact of adaptive proton therapy in head and neck cancer – A review
title_short Dosimetric impact of adaptive proton therapy in head and neck cancer – A review
title_sort dosimetric impact of adaptive proton therapy in head and neck cancer – a review
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9969246/
https://www.ncbi.nlm.nih.gov/pubmed/36860581
http://dx.doi.org/10.1016/j.ctro.2023.100598
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