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Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes

BACKGROUND: Delivery of SBRT to central thoracic tumours within 2 cm of the proximal bronchial tree (PBT), and especially ultra-central tumours which directly abut the PBT, has been controversial due to concerns about high risk of toxicity and treatment-related death when delivering high doses close...

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Autores principales: Cooke, Rosie, Camilleri, Philip, Chu, Kwun-Ye, O'Cathail, Séan M., Robinson, Maxwell, Van Den Heuvel, Frank, Hawkins, Maria A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042153/
https://www.ncbi.nlm.nih.gov/pubmed/32128460
http://dx.doi.org/10.1016/j.tipsro.2020.01.002
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author Cooke, Rosie
Camilleri, Philip
Chu, Kwun-Ye
O'Cathail, Séan M.
Robinson, Maxwell
Van Den Heuvel, Frank
Hawkins, Maria A.
author_facet Cooke, Rosie
Camilleri, Philip
Chu, Kwun-Ye
O'Cathail, Séan M.
Robinson, Maxwell
Van Den Heuvel, Frank
Hawkins, Maria A.
author_sort Cooke, Rosie
collection PubMed
description BACKGROUND: Delivery of SBRT to central thoracic tumours within 2 cm of the proximal bronchial tree (PBT), and especially ultra-central tumours which directly abut the PBT, has been controversial due to concerns about high risk of toxicity and treatment-related death when delivering high doses close to critical mediastinal structures. We present dosimetric and clinical outcomes from a group of oligometastatic patients treated with a risk-adapted SBRT approach. METHODS: Between September 2015 and October 2018, 27 patients with 28 central thoracic oligometastases (6 moderately central, 22 ultra-central) were treated with 60 Gy in 8 fractions under online CBCT guidance. PTV dose was compromised where necessary to meet mandatory OAR constraints. Patients were followed up for toxicity and disease status. RESULTS: Mandatory OAR constraints were met in all cases; this required PTV coverage compromise in 23 cases, with V100% reduced to <70% in 11 cases. No acute or late toxicities of Grade ≥ 3 were reported. One and 2 year in-field control rates were 95.2% and 85.7% respectively, progression-free survival rates were 42.8% and 23.4% respectively, and overall survival rates were 82.7% and 69.5% respectively. No significant differences were seen in control or survival rates by extent of PTV underdosage or between moderately and ultra-central cases. CONCLUSION: It appears that compromising PTV coverage to meet OAR constraints allows safe and effective delivery of SBRT to moderately and ultra-central tumours, with low toxicity rates and high in-field control rates. This treatment can be delivered on standard linear accelerators with widely available imaging technology.
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spelling pubmed-70421532020-03-03 Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes Cooke, Rosie Camilleri, Philip Chu, Kwun-Ye O'Cathail, Séan M. Robinson, Maxwell Van Den Heuvel, Frank Hawkins, Maria A. Tech Innov Patient Support Radiat Oncol Research article BACKGROUND: Delivery of SBRT to central thoracic tumours within 2 cm of the proximal bronchial tree (PBT), and especially ultra-central tumours which directly abut the PBT, has been controversial due to concerns about high risk of toxicity and treatment-related death when delivering high doses close to critical mediastinal structures. We present dosimetric and clinical outcomes from a group of oligometastatic patients treated with a risk-adapted SBRT approach. METHODS: Between September 2015 and October 2018, 27 patients with 28 central thoracic oligometastases (6 moderately central, 22 ultra-central) were treated with 60 Gy in 8 fractions under online CBCT guidance. PTV dose was compromised where necessary to meet mandatory OAR constraints. Patients were followed up for toxicity and disease status. RESULTS: Mandatory OAR constraints were met in all cases; this required PTV coverage compromise in 23 cases, with V100% reduced to <70% in 11 cases. No acute or late toxicities of Grade ≥ 3 were reported. One and 2 year in-field control rates were 95.2% and 85.7% respectively, progression-free survival rates were 42.8% and 23.4% respectively, and overall survival rates were 82.7% and 69.5% respectively. No significant differences were seen in control or survival rates by extent of PTV underdosage or between moderately and ultra-central cases. CONCLUSION: It appears that compromising PTV coverage to meet OAR constraints allows safe and effective delivery of SBRT to moderately and ultra-central tumours, with low toxicity rates and high in-field control rates. This treatment can be delivered on standard linear accelerators with widely available imaging technology. Elsevier 2020-02-17 /pmc/articles/PMC7042153/ /pubmed/32128460 http://dx.doi.org/10.1016/j.tipsro.2020.01.002 Text en © 2020 The Authors 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
Cooke, Rosie
Camilleri, Philip
Chu, Kwun-Ye
O'Cathail, Séan M.
Robinson, Maxwell
Van Den Heuvel, Frank
Hawkins, Maria A.
Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes
title Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes
title_full Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes
title_fullStr Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes
title_full_unstemmed Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes
title_short Stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: Initial outcomes
title_sort stereotactic body radiotherapy for moderately central and ultra-central oligometastatic disease: initial outcomes
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7042153/
https://www.ncbi.nlm.nih.gov/pubmed/32128460
http://dx.doi.org/10.1016/j.tipsro.2020.01.002
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