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Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer

BACKGROUND: The aim of this work was to investigate the outcome of metastasis-directed radiotherapy (MDT) in prostate cancer patients with bone metastases following current ESTRO/EORTC subclassifications for oligometastatic disease. METHODS: Clinical data of 80 consecutive oligometastatic patients w...

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Autores principales: Rogowski, Paul, Trapp, Christian, von Bestenbostel, Rieke, Schmidt-Hegemann, Nina-Sophie, Shi, Run, Ilhan, Harun, Kretschmer, Alexander, Stief, Christian, Ganswindt, Ute, Belka, Claus, Li, Minglun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247211/
https://www.ncbi.nlm.nih.gov/pubmed/34193194
http://dx.doi.org/10.1186/s13014-021-01849-8
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author Rogowski, Paul
Trapp, Christian
von Bestenbostel, Rieke
Schmidt-Hegemann, Nina-Sophie
Shi, Run
Ilhan, Harun
Kretschmer, Alexander
Stief, Christian
Ganswindt, Ute
Belka, Claus
Li, Minglun
author_facet Rogowski, Paul
Trapp, Christian
von Bestenbostel, Rieke
Schmidt-Hegemann, Nina-Sophie
Shi, Run
Ilhan, Harun
Kretschmer, Alexander
Stief, Christian
Ganswindt, Ute
Belka, Claus
Li, Minglun
author_sort Rogowski, Paul
collection PubMed
description BACKGROUND: The aim of this work was to investigate the outcome of metastasis-directed radiotherapy (MDT) in prostate cancer patients with bone metastases following current ESTRO/EORTC subclassifications for oligometastatic disease. METHODS: Clinical data of 80 consecutive oligometastatic patients with 115 bone lesions receiving MDT between 2011 and 2019 were retrospectively evaluated. Hormone-sensitive (77.5%) and castrate-resistant (22.5%) patients were included. MDT was delivered with conventional fractionated or stereotactic body radiotherapy (SBRT) techniques. Kaplan–Meier method, log rank test, as well as Cox regression were used to calculate local control (LC) and biochemical and clinical progression-free survival (bPFS/cPFS). RESULTS: At the time of MDT 31% of patients had de-novo synchronous oligometastatic disease, 46% had de-novo metachronous oligorecurrence after primary treatment and 23% had either de-novo oligoprogressive disease, repeat oligometastatic disease or induced oligometastatic disease. The median BED(3) was 93.3 Gy (range 75.8–95.3 Gy). Concomitant ADT was administered in 69% of patients. After a median follow-up of 23 months the median bPFS and cPFS were 16.5 and 21.5 months, respectively. The 2-year LC rate was 98.3%. In multivariate analysis, age ≤ 70 (HR = 2.60, 95% CI 1.20–5.62, p = 0.015) and concomitant ADT (HR = 0.26, 95% CI 0.12–0.58, p = 0.001) significantly correlated with cPFS. Category of oligometastatic disease and hormone-sensitivity were predictive for cPFS in univariate analysis. Of 45 patients with biochemical relapse, nineteen patients (42.2%) had repeat oligometastatic disease. Fourteen patients (31%) underwent a second course of MDT. No patients experienced grade ≥ 3 toxicities. CONCLUSIONS: MDT is safe and offers high local control rates in bone oligometastases of prostate cancer. At 2 years after treatment, more than 2 out of 5 patients are progression-free. Trial registration Retrospectively registered.
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spelling pubmed-82472112021-07-06 Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer Rogowski, Paul Trapp, Christian von Bestenbostel, Rieke Schmidt-Hegemann, Nina-Sophie Shi, Run Ilhan, Harun Kretschmer, Alexander Stief, Christian Ganswindt, Ute Belka, Claus Li, Minglun Radiat Oncol Research BACKGROUND: The aim of this work was to investigate the outcome of metastasis-directed radiotherapy (MDT) in prostate cancer patients with bone metastases following current ESTRO/EORTC subclassifications for oligometastatic disease. METHODS: Clinical data of 80 consecutive oligometastatic patients with 115 bone lesions receiving MDT between 2011 and 2019 were retrospectively evaluated. Hormone-sensitive (77.5%) and castrate-resistant (22.5%) patients were included. MDT was delivered with conventional fractionated or stereotactic body radiotherapy (SBRT) techniques. Kaplan–Meier method, log rank test, as well as Cox regression were used to calculate local control (LC) and biochemical and clinical progression-free survival (bPFS/cPFS). RESULTS: At the time of MDT 31% of patients had de-novo synchronous oligometastatic disease, 46% had de-novo metachronous oligorecurrence after primary treatment and 23% had either de-novo oligoprogressive disease, repeat oligometastatic disease or induced oligometastatic disease. The median BED(3) was 93.3 Gy (range 75.8–95.3 Gy). Concomitant ADT was administered in 69% of patients. After a median follow-up of 23 months the median bPFS and cPFS were 16.5 and 21.5 months, respectively. The 2-year LC rate was 98.3%. In multivariate analysis, age ≤ 70 (HR = 2.60, 95% CI 1.20–5.62, p = 0.015) and concomitant ADT (HR = 0.26, 95% CI 0.12–0.58, p = 0.001) significantly correlated with cPFS. Category of oligometastatic disease and hormone-sensitivity were predictive for cPFS in univariate analysis. Of 45 patients with biochemical relapse, nineteen patients (42.2%) had repeat oligometastatic disease. Fourteen patients (31%) underwent a second course of MDT. No patients experienced grade ≥ 3 toxicities. CONCLUSIONS: MDT is safe and offers high local control rates in bone oligometastases of prostate cancer. At 2 years after treatment, more than 2 out of 5 patients are progression-free. Trial registration Retrospectively registered. BioMed Central 2021-06-30 /pmc/articles/PMC8247211/ /pubmed/34193194 http://dx.doi.org/10.1186/s13014-021-01849-8 Text en © The Author(s) 2021 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
Rogowski, Paul
Trapp, Christian
von Bestenbostel, Rieke
Schmidt-Hegemann, Nina-Sophie
Shi, Run
Ilhan, Harun
Kretschmer, Alexander
Stief, Christian
Ganswindt, Ute
Belka, Claus
Li, Minglun
Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
title Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
title_full Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
title_fullStr Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
title_full_unstemmed Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
title_short Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
title_sort outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8247211/
https://www.ncbi.nlm.nih.gov/pubmed/34193194
http://dx.doi.org/10.1186/s13014-021-01849-8
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