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Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases

BACKGROUND: Patients with oligometastatic disease can potentially be cured by using an ablative therapy for all active lesions. Stereotactic body radiotherapy (SBRT) is a non-invasive treatment option that lately proved to be as effective and safe as surgery in treating lung metastases (LM). However...

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Autores principales: Kalinauskaite, Goda G., Tinhofer, Ingeborg I., Kufeld, Markus M., Kluge, Anne A., Grün, Arne A., Budach, Volker V., Senger, Carolin C., Stromberger, Carmen C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216666/
https://www.ncbi.nlm.nih.gov/pubmed/32393261
http://dx.doi.org/10.1186/s12885-020-06892-4
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author Kalinauskaite, Goda G.
Tinhofer, Ingeborg I.
Kufeld, Markus M.
Kluge, Anne A.
Grün, Arne A.
Budach, Volker V.
Senger, Carolin C.
Stromberger, Carmen C.
author_facet Kalinauskaite, Goda G.
Tinhofer, Ingeborg I.
Kufeld, Markus M.
Kluge, Anne A.
Grün, Arne A.
Budach, Volker V.
Senger, Carolin C.
Stromberger, Carmen C.
author_sort Kalinauskaite, Goda G.
collection PubMed
description BACKGROUND: Patients with oligometastatic disease can potentially be cured by using an ablative therapy for all active lesions. Stereotactic body radiotherapy (SBRT) is a non-invasive treatment option that lately proved to be as effective and safe as surgery in treating lung metastases (LM). However, it is not clear which patients benefit most and what are the most suitable fractionation regimens. The aim of this study was to analyze treatment outcomes after single fraction radiosurgery (SFRS) and fractionated SBRT (fSBRT) in patients with lung oligometastases and identify prognostic clinical features for better survival outcomes. METHODS: Fifty-two patients with 94 LM treated with SFRS or fSBRT between 2010 and 2016 were analyzed. The characteristics of primary tumor, LM, treatment, toxicity profiles and outcomes were assessed. Kaplan-Meier and Cox regression analyses were used for estimation of local control (LC), overall survival (OS) and progression-free survival. RESULTS: Ninety-four LM in 52 patients were treated using SFRS/fSBRT with a median of 2 lesions per patient (range: 1–5). The median planning target volume (PTV)-encompassing dose for SFRS was 24 Gy (range: 17–26) compared to 45 Gy (range: 20–60) in 2–12 fractions with fSBRT. The median follow-up time was 21 months (range: 3–68). LC rates at 1 and 2 years for SFSR vs. fSBRT were 89 and 83% vs. 75 and 59%, respectively (p = 0.026). LM treated with SFSR were significantly smaller (p = 0.001). The 1 and 2-year OS rates for all patients were 84 and 71%, respectively. In univariate analysis treatment with SFRS, an interval of ≥12 months between diagnosis of LM and treatment, non-colorectal cancer histology and BED < 100 Gy were significantly associated with better LC. However, none of these parameters remained significant in the multivariate Cox regression model. OS was significantly better in patients with negative lymph nodes (N0), Karnofsky performance status (KPS) > 70% and time to first metastasis ≥12 months. There was no grade 3 acute or late toxicity. CONCLUSIONS: Longer time to first metastasis, good KPS and N0 predicted better OS. Good LC and low toxicity rates were achieved after short SBRT schedules.
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spelling pubmed-72166662020-05-18 Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases Kalinauskaite, Goda G. Tinhofer, Ingeborg I. Kufeld, Markus M. Kluge, Anne A. Grün, Arne A. Budach, Volker V. Senger, Carolin C. Stromberger, Carmen C. BMC Cancer Research Article BACKGROUND: Patients with oligometastatic disease can potentially be cured by using an ablative therapy for all active lesions. Stereotactic body radiotherapy (SBRT) is a non-invasive treatment option that lately proved to be as effective and safe as surgery in treating lung metastases (LM). However, it is not clear which patients benefit most and what are the most suitable fractionation regimens. The aim of this study was to analyze treatment outcomes after single fraction radiosurgery (SFRS) and fractionated SBRT (fSBRT) in patients with lung oligometastases and identify prognostic clinical features for better survival outcomes. METHODS: Fifty-two patients with 94 LM treated with SFRS or fSBRT between 2010 and 2016 were analyzed. The characteristics of primary tumor, LM, treatment, toxicity profiles and outcomes were assessed. Kaplan-Meier and Cox regression analyses were used for estimation of local control (LC), overall survival (OS) and progression-free survival. RESULTS: Ninety-four LM in 52 patients were treated using SFRS/fSBRT with a median of 2 lesions per patient (range: 1–5). The median planning target volume (PTV)-encompassing dose for SFRS was 24 Gy (range: 17–26) compared to 45 Gy (range: 20–60) in 2–12 fractions with fSBRT. The median follow-up time was 21 months (range: 3–68). LC rates at 1 and 2 years for SFSR vs. fSBRT were 89 and 83% vs. 75 and 59%, respectively (p = 0.026). LM treated with SFSR were significantly smaller (p = 0.001). The 1 and 2-year OS rates for all patients were 84 and 71%, respectively. In univariate analysis treatment with SFRS, an interval of ≥12 months between diagnosis of LM and treatment, non-colorectal cancer histology and BED < 100 Gy were significantly associated with better LC. However, none of these parameters remained significant in the multivariate Cox regression model. OS was significantly better in patients with negative lymph nodes (N0), Karnofsky performance status (KPS) > 70% and time to first metastasis ≥12 months. There was no grade 3 acute or late toxicity. CONCLUSIONS: Longer time to first metastasis, good KPS and N0 predicted better OS. Good LC and low toxicity rates were achieved after short SBRT schedules. BioMed Central 2020-05-11 /pmc/articles/PMC7216666/ /pubmed/32393261 http://dx.doi.org/10.1186/s12885-020-06892-4 Text en © The Author(s) 2020 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/. 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 in a credit line to the data.
spellingShingle Research Article
Kalinauskaite, Goda G.
Tinhofer, Ingeborg I.
Kufeld, Markus M.
Kluge, Anne A.
Grün, Arne A.
Budach, Volker V.
Senger, Carolin C.
Stromberger, Carmen C.
Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
title Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
title_full Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
title_fullStr Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
title_full_unstemmed Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
title_short Radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
title_sort radiosurgery and fractionated stereotactic body radiotherapy for patients with lung oligometastases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216666/
https://www.ncbi.nlm.nih.gov/pubmed/32393261
http://dx.doi.org/10.1186/s12885-020-06892-4
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