Cargando…
Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk?
BACKGROUND: Lung stereotactic ablative radiotherapy (SABR) is associated with low morbidity, however there is an increased risk of treatment-related toxicity in tumors directly abutting or invading the proximal bronchial tree, termed ‘ultra-central’ tumors. As there is no consensus regarding the opt...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880025/ https://www.ncbi.nlm.nih.gov/pubmed/29606150 http://dx.doi.org/10.1186/s13014-018-1001-6 |
_version_ | 1783311104027394048 |
---|---|
author | Murrell, Donna H. Laba, Joanna M. Erickson, Abigail Millman, Barbara Palma, David A. Louie, Alexander V. |
author_facet | Murrell, Donna H. Laba, Joanna M. Erickson, Abigail Millman, Barbara Palma, David A. Louie, Alexander V. |
author_sort | Murrell, Donna H. |
collection | PubMed |
description | BACKGROUND: Lung stereotactic ablative radiotherapy (SABR) is associated with low morbidity, however there is an increased risk of treatment-related toxicity in tumors directly abutting or invading the proximal bronchial tree, termed ‘ultra-central’ tumors. As there is no consensus regarding the optimal radiotherapy treatment regimen for these tumors, we performed a modeling study to evaluate the trade-offs between predicted toxicity and local control for commonly used high-precision dose-fractionation regimens. METHODS: Ten patients with ultra-central lung tumors were identified from our institutional database. New plans were generated for 3 different hypofractionated schemes: 50 Gy in 5 fractions, 60 Gy in 8 fractions and 60 Gy in 15 fractions. For each regimen, one plan was created that prioritized planning target volume (PTV) coverage, potentially at the expense of organ at risk (OAR) tolerance, and a second that compromised PTV coverage to respect OAR dose constraints. Published radiobiological models were employed to evaluate competing treatment plans based on estimates for local control and the likelihood for toxicity to OAR. RESULTS: The risk of esophageal or pulmonary toxicity was low (< 5%) in all scenarios. When PTV coverage was prioritized, tumor control probabilities were 92.9% for 50 Gy in 5 fractions, 92.4% for 60 Gy in 8 fractions, and 52.0% for 60 Gy in 15 fractions; however the estimated risk of grade ≥ 4 toxicity to the proximal bronchial tree was 68%, 44% and 2% respectively. When dose to OAR was prioritized, the risk of major pulmonary toxicity was reduced to < 1% in all schemes, but this compromise reduced tumor control probability to 60.3% for 50 Gy in 5 fractions, 65.7% for 60 Gy in 8 fractions and 47.8% for 60 Gy in 15 fractions. CONCLUSIONS: The tradeoff between local control and central airway toxicity are considerable in the use of 3 commonly used hypofractionated radiotherapy regimens for ultra-central lung cancer. The results of this planning study predict that the best balance may be achieved with 60 Gy in 8 fractions compromising PTV coverage as required to maintain acceptable doses to OAR. A prospective phase I trial (SUNSET) is planned to further evaluate this challenging clinical scenario. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13014-018-1001-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5880025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58800252018-04-04 Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? Murrell, Donna H. Laba, Joanna M. Erickson, Abigail Millman, Barbara Palma, David A. Louie, Alexander V. Radiat Oncol Research BACKGROUND: Lung stereotactic ablative radiotherapy (SABR) is associated with low morbidity, however there is an increased risk of treatment-related toxicity in tumors directly abutting or invading the proximal bronchial tree, termed ‘ultra-central’ tumors. As there is no consensus regarding the optimal radiotherapy treatment regimen for these tumors, we performed a modeling study to evaluate the trade-offs between predicted toxicity and local control for commonly used high-precision dose-fractionation regimens. METHODS: Ten patients with ultra-central lung tumors were identified from our institutional database. New plans were generated for 3 different hypofractionated schemes: 50 Gy in 5 fractions, 60 Gy in 8 fractions and 60 Gy in 15 fractions. For each regimen, one plan was created that prioritized planning target volume (PTV) coverage, potentially at the expense of organ at risk (OAR) tolerance, and a second that compromised PTV coverage to respect OAR dose constraints. Published radiobiological models were employed to evaluate competing treatment plans based on estimates for local control and the likelihood for toxicity to OAR. RESULTS: The risk of esophageal or pulmonary toxicity was low (< 5%) in all scenarios. When PTV coverage was prioritized, tumor control probabilities were 92.9% for 50 Gy in 5 fractions, 92.4% for 60 Gy in 8 fractions, and 52.0% for 60 Gy in 15 fractions; however the estimated risk of grade ≥ 4 toxicity to the proximal bronchial tree was 68%, 44% and 2% respectively. When dose to OAR was prioritized, the risk of major pulmonary toxicity was reduced to < 1% in all schemes, but this compromise reduced tumor control probability to 60.3% for 50 Gy in 5 fractions, 65.7% for 60 Gy in 8 fractions and 47.8% for 60 Gy in 15 fractions. CONCLUSIONS: The tradeoff between local control and central airway toxicity are considerable in the use of 3 commonly used hypofractionated radiotherapy regimens for ultra-central lung cancer. The results of this planning study predict that the best balance may be achieved with 60 Gy in 8 fractions compromising PTV coverage as required to maintain acceptable doses to OAR. A prospective phase I trial (SUNSET) is planned to further evaluate this challenging clinical scenario. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13014-018-1001-6) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-02 /pmc/articles/PMC5880025/ /pubmed/29606150 http://dx.doi.org/10.1186/s13014-018-1001-6 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Murrell, Donna H. Laba, Joanna M. Erickson, Abigail Millman, Barbara Palma, David A. Louie, Alexander V. Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
title | Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
title_full | Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
title_fullStr | Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
title_full_unstemmed | Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
title_short | Stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
title_sort | stereotactic ablative radiotherapy for ultra-central lung tumors: prioritize target coverage or organs at risk? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5880025/ https://www.ncbi.nlm.nih.gov/pubmed/29606150 http://dx.doi.org/10.1186/s13014-018-1001-6 |
work_keys_str_mv | AT murrelldonnah stereotacticablativeradiotherapyforultracentrallungtumorsprioritizetargetcoverageororgansatrisk AT labajoannam stereotacticablativeradiotherapyforultracentrallungtumorsprioritizetargetcoverageororgansatrisk AT ericksonabigail stereotacticablativeradiotherapyforultracentrallungtumorsprioritizetargetcoverageororgansatrisk AT millmanbarbara stereotacticablativeradiotherapyforultracentrallungtumorsprioritizetargetcoverageororgansatrisk AT palmadavida stereotacticablativeradiotherapyforultracentrallungtumorsprioritizetargetcoverageororgansatrisk AT louiealexanderv stereotacticablativeradiotherapyforultracentrallungtumorsprioritizetargetcoverageororgansatrisk |