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Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study

BACKGROUND: Radiation therapy, especially the development of linear accelerators, plays a key role in cancer management. The fast-rotating coplanar O-ring Halcyon Linac has demonstrated many advantages. The previous literature has mainly focused on the machine parameters and plan quality of Halcyon,...

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Autores principales: Wang, Guang-Yu, Zhu, Qi-Zhen, Zhu, He-Ling, Jiang, Ling-Juan, Zhao, Nan, Liu, Zhi-Kai, Zhang, Fu-Quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372831/
https://www.ncbi.nlm.nih.gov/pubmed/36158510
http://dx.doi.org/10.12998/wjcc.v10.i22.7728
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author Wang, Guang-Yu
Zhu, Qi-Zhen
Zhu, He-Ling
Jiang, Ling-Juan
Zhao, Nan
Liu, Zhi-Kai
Zhang, Fu-Quan
author_facet Wang, Guang-Yu
Zhu, Qi-Zhen
Zhu, He-Ling
Jiang, Ling-Juan
Zhao, Nan
Liu, Zhi-Kai
Zhang, Fu-Quan
author_sort Wang, Guang-Yu
collection PubMed
description BACKGROUND: Radiation therapy, especially the development of linear accelerators, plays a key role in cancer management. The fast-rotating coplanar O-ring Halcyon Linac has demonstrated many advantages. The previous literature has mainly focused on the machine parameters and plan quality of Halcyon, with a lack of relevant research on its clinical application. AIM: To evaluate the clinical performance of the O-ring Halcyon treatment system in a real-world application setting. METHODS: Data from sixty-one patients who were treated with the Halcyon system throughout the entire radiotherapy process in Peking Union Medical College Hospital between August 2019 and September 2020 were retrospectively reviewed. We evaluated the target tumour response to radiotherapy and irradiation toxicity from 1 to 3 mo after treatment. Dosimetric verification of Halcyon plans was performed using a quality assurance procedure, including portal dosimetry, ArcCHECK and point dose measurements for verification of the system delivery accuracy. RESULTS: Of the 61 patients in the five groups, 16, 12, 7 and 26 patients had complete response, partial response, progressive disease and stable disease, respectively. No increase in the irradiated target tumour volume was observed when separately evaluating the local response. Regarding irradiation toxicity, no radiation-induced deaths were observed. Thirty-eight percent (23/61 patients) had no radiation toxicity after radiotherapy, 56% (34/61 patients) experienced radiation toxicity that resolved after treatment, and 6% (4/61 patients) had irreversible adverse reactions. The average gamma passing rates with a 2% dose difference and 2-mm distance to agreement for IMRT/VMAT/SRT plans were ArcCHECK at 96.4% and portal dosimetry at 96.7%, respectively. All of the validated clinical plans were within 3% for point dose measurements, and Halcyon’s ArcCHECK demonstrated a high pass rate of 99.1% ± 1.1% for clinical gamma passing criteria of 3%/3 mm. CONCLUSION: The O-ring Halcyon Linac could achieve a better therapeutic effect on the target volume by providing accurate treatment delivery plans with tolerable irradiation toxicity.
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spelling pubmed-93728312022-09-23 Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study Wang, Guang-Yu Zhu, Qi-Zhen Zhu, He-Ling Jiang, Ling-Juan Zhao, Nan Liu, Zhi-Kai Zhang, Fu-Quan World J Clin Cases Retrospective Study BACKGROUND: Radiation therapy, especially the development of linear accelerators, plays a key role in cancer management. The fast-rotating coplanar O-ring Halcyon Linac has demonstrated many advantages. The previous literature has mainly focused on the machine parameters and plan quality of Halcyon, with a lack of relevant research on its clinical application. AIM: To evaluate the clinical performance of the O-ring Halcyon treatment system in a real-world application setting. METHODS: Data from sixty-one patients who were treated with the Halcyon system throughout the entire radiotherapy process in Peking Union Medical College Hospital between August 2019 and September 2020 were retrospectively reviewed. We evaluated the target tumour response to radiotherapy and irradiation toxicity from 1 to 3 mo after treatment. Dosimetric verification of Halcyon plans was performed using a quality assurance procedure, including portal dosimetry, ArcCHECK and point dose measurements for verification of the system delivery accuracy. RESULTS: Of the 61 patients in the five groups, 16, 12, 7 and 26 patients had complete response, partial response, progressive disease and stable disease, respectively. No increase in the irradiated target tumour volume was observed when separately evaluating the local response. Regarding irradiation toxicity, no radiation-induced deaths were observed. Thirty-eight percent (23/61 patients) had no radiation toxicity after radiotherapy, 56% (34/61 patients) experienced radiation toxicity that resolved after treatment, and 6% (4/61 patients) had irreversible adverse reactions. The average gamma passing rates with a 2% dose difference and 2-mm distance to agreement for IMRT/VMAT/SRT plans were ArcCHECK at 96.4% and portal dosimetry at 96.7%, respectively. All of the validated clinical plans were within 3% for point dose measurements, and Halcyon’s ArcCHECK demonstrated a high pass rate of 99.1% ± 1.1% for clinical gamma passing criteria of 3%/3 mm. CONCLUSION: The O-ring Halcyon Linac could achieve a better therapeutic effect on the target volume by providing accurate treatment delivery plans with tolerable irradiation toxicity. Baishideng Publishing Group Inc 2022-08-06 2022-08-06 /pmc/articles/PMC9372831/ /pubmed/36158510 http://dx.doi.org/10.12998/wjcc.v10.i22.7728 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Retrospective Study
Wang, Guang-Yu
Zhu, Qi-Zhen
Zhu, He-Ling
Jiang, Ling-Juan
Zhao, Nan
Liu, Zhi-Kai
Zhang, Fu-Quan
Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study
title Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study
title_full Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study
title_fullStr Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study
title_full_unstemmed Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study
title_short Clinical performance evaluation of O-Ring Halcyon Linac: A real-world study
title_sort clinical performance evaluation of o-ring halcyon linac: a real-world study
topic Retrospective Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9372831/
https://www.ncbi.nlm.nih.gov/pubmed/36158510
http://dx.doi.org/10.12998/wjcc.v10.i22.7728
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