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Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer
BACKGROUND: Daily adaptive radiation therapy (ART) of patients with non-small cell lung cancer (NSCLC) lowers organs at risk exposure while maintaining the planning target volume (PTV) coverage. Thus, ART allows an isotoxic approach with increased doses to the PTV that could improve local tumor cont...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945670/ https://www.ncbi.nlm.nih.gov/pubmed/36814271 http://dx.doi.org/10.1186/s13014-023-02222-7 |
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author | Hoppen, Lea Sarria, Gustavo R. Kwok, Chung S. Boda-Heggemann, Judit Buergy, Daniel Ehmann, Michael Giordano, Frank A. Fleckenstein, Jens |
author_facet | Hoppen, Lea Sarria, Gustavo R. Kwok, Chung S. Boda-Heggemann, Judit Buergy, Daniel Ehmann, Michael Giordano, Frank A. Fleckenstein, Jens |
author_sort | Hoppen, Lea |
collection | PubMed |
description | BACKGROUND: Daily adaptive radiation therapy (ART) of patients with non-small cell lung cancer (NSCLC) lowers organs at risk exposure while maintaining the planning target volume (PTV) coverage. Thus, ART allows an isotoxic approach with increased doses to the PTV that could improve local tumor control. Herein we evaluate daily online ART strategies regarding their impact on relevant dose-volume metrics. METHODS: Daily cone-beam CTs (1 × n = 28, 1 × n = 29, 11 × n = 30) of 13 stage III NSCLC patients were converted into synthetic CTs (sCTs). Treatment plans (TPs) were created retrospectively on the first-fraction sCTs (sCT(1)) and subsequently transferred unaltered to the sCTs of the remaining fractions of each patient (sCT(2−n)) (IGRT scenario). Two additional TPs were generated on sCT(2−n): one minimizing the lung-dose while preserving the D(95%)(PTV) (isoeffective scenario), the other escalating the D(95%)(PTV) with a constant V(20Gy)(lung(ipsilateral)) (isotoxic scenario). RESULTS: Compared to the original TPs predicted dose, the median D(95%)(PTV) in the IGRT scenario decreased by 1.6 Gy ± 4.2 Gy while the V(20Gy)(lung(ipsilateral)) increased in median by 1.1% ± 4.4%. The isoeffective scenario preserved the PTV coverage and reduced the median V(20Gy)(lung(ipsilateral)) by 3.1% ± 3.6%. Furthermore, the median V(5%)(heart) decreased by 2.9% ± 6.4%. With an isotoxic prescription, a median dose-escalation to the gross target volume of 10.0 Gy ± 8.1 Gy without increasing the V(20Gy)(lung(ipsilateral)) and V(5%)(heart) was feasible. CONCLUSIONS: We demonstrated that even without reducing safety margins, ART can reduce lung-doses, while still reaching adequate target coverage or escalate target doses without increasing ipsilateral lung exposure. Clinical benefits by means of toxicity and local control of both strategies should be evaluated in prospective clinical trials. |
format | Online Article Text |
id | pubmed-9945670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-99456702023-02-23 Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer Hoppen, Lea Sarria, Gustavo R. Kwok, Chung S. Boda-Heggemann, Judit Buergy, Daniel Ehmann, Michael Giordano, Frank A. Fleckenstein, Jens Radiat Oncol Research BACKGROUND: Daily adaptive radiation therapy (ART) of patients with non-small cell lung cancer (NSCLC) lowers organs at risk exposure while maintaining the planning target volume (PTV) coverage. Thus, ART allows an isotoxic approach with increased doses to the PTV that could improve local tumor control. Herein we evaluate daily online ART strategies regarding their impact on relevant dose-volume metrics. METHODS: Daily cone-beam CTs (1 × n = 28, 1 × n = 29, 11 × n = 30) of 13 stage III NSCLC patients were converted into synthetic CTs (sCTs). Treatment plans (TPs) were created retrospectively on the first-fraction sCTs (sCT(1)) and subsequently transferred unaltered to the sCTs of the remaining fractions of each patient (sCT(2−n)) (IGRT scenario). Two additional TPs were generated on sCT(2−n): one minimizing the lung-dose while preserving the D(95%)(PTV) (isoeffective scenario), the other escalating the D(95%)(PTV) with a constant V(20Gy)(lung(ipsilateral)) (isotoxic scenario). RESULTS: Compared to the original TPs predicted dose, the median D(95%)(PTV) in the IGRT scenario decreased by 1.6 Gy ± 4.2 Gy while the V(20Gy)(lung(ipsilateral)) increased in median by 1.1% ± 4.4%. The isoeffective scenario preserved the PTV coverage and reduced the median V(20Gy)(lung(ipsilateral)) by 3.1% ± 3.6%. Furthermore, the median V(5%)(heart) decreased by 2.9% ± 6.4%. With an isotoxic prescription, a median dose-escalation to the gross target volume of 10.0 Gy ± 8.1 Gy without increasing the V(20Gy)(lung(ipsilateral)) and V(5%)(heart) was feasible. CONCLUSIONS: We demonstrated that even without reducing safety margins, ART can reduce lung-doses, while still reaching adequate target coverage or escalate target doses without increasing ipsilateral lung exposure. Clinical benefits by means of toxicity and local control of both strategies should be evaluated in prospective clinical trials. BioMed Central 2023-02-22 /pmc/articles/PMC9945670/ /pubmed/36814271 http://dx.doi.org/10.1186/s13014-023-02222-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Hoppen, Lea Sarria, Gustavo R. Kwok, Chung S. Boda-Heggemann, Judit Buergy, Daniel Ehmann, Michael Giordano, Frank A. Fleckenstein, Jens Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer |
title | Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer |
title_full | Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer |
title_fullStr | Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer |
title_full_unstemmed | Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer |
title_short | Dosimetric benefits of adaptive radiation therapy for patients with stage III non-small cell lung cancer |
title_sort | dosimetric benefits of adaptive radiation therapy for patients with stage iii non-small cell lung cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945670/ https://www.ncbi.nlm.nih.gov/pubmed/36814271 http://dx.doi.org/10.1186/s13014-023-02222-7 |
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