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Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study
To evaluate the effects and toxicity of radiotherapy (RT) combined with androgen deprivation (AD) for bone oligometastases after primary curative RT for prostate cancer (PCa). We retrospectively analyzed 30 consecutively treated PCa patients with bone oligometastases from April 2005 to July 2014. Al...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753934/ https://www.ncbi.nlm.nih.gov/pubmed/26871838 http://dx.doi.org/10.1097/MD.0000000000002789 |
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author | Wu, Jun-Xin Lin, Li-Mei He, Jun-Yan Hong, Liang Li, Jin-Luan |
author_facet | Wu, Jun-Xin Lin, Li-Mei He, Jun-Yan Hong, Liang Li, Jin-Luan |
author_sort | Wu, Jun-Xin |
collection | PubMed |
description | To evaluate the effects and toxicity of radiotherapy (RT) combined with androgen deprivation (AD) for bone oligometastases after primary curative RT for prostate cancer (PCa). We retrospectively analyzed 30 consecutively treated PCa patients with bone oligometastases from April 2005 to July 2014. All patients underwent RT combined with AD for oligometastatic bones after curative RT for PCa. Measured outcomes included overall survival (OS) rate, local control (LC), progression-free survival (PFS), pain relief, and toxicities. Statistical analysis was performed with SPSS17.0. The median follow-up was 32.5 months (range, 0.6–50.3). The 3-year PFS and OS rates were 22.8% (95% CI, 13.4–37.5%) and 69% (95% CI, 51.7–81.1%), respectively. The number of bone oligometastases and RT schedule were found to be significantly associated with OS on univariate analysis (P < 0.05, respectively). The 3-year OS for patients with 1 and >1 metastases was 78.8% versus 42.2%, respectively (P = 0.037). The long-course RT was associated with better 3-year OS compared with short-course (76.4% vs 44.1%, P = 0.03). A total of 15 (83.3%, 15/18) patients achieved pain relief. No grade 3 toxicity was observed. Long-course RT combined with ADT was effective and well-tolerated in PCa patients with bone oligometastases after curative RT for PCa. Further randomized controlled trials are needed to corroborate the findings. |
format | Online Article Text |
id | pubmed-4753934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-47539342016-02-26 Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study Wu, Jun-Xin Lin, Li-Mei He, Jun-Yan Hong, Liang Li, Jin-Luan Medicine (Baltimore) 5700 To evaluate the effects and toxicity of radiotherapy (RT) combined with androgen deprivation (AD) for bone oligometastases after primary curative RT for prostate cancer (PCa). We retrospectively analyzed 30 consecutively treated PCa patients with bone oligometastases from April 2005 to July 2014. All patients underwent RT combined with AD for oligometastatic bones after curative RT for PCa. Measured outcomes included overall survival (OS) rate, local control (LC), progression-free survival (PFS), pain relief, and toxicities. Statistical analysis was performed with SPSS17.0. The median follow-up was 32.5 months (range, 0.6–50.3). The 3-year PFS and OS rates were 22.8% (95% CI, 13.4–37.5%) and 69% (95% CI, 51.7–81.1%), respectively. The number of bone oligometastases and RT schedule were found to be significantly associated with OS on univariate analysis (P < 0.05, respectively). The 3-year OS for patients with 1 and >1 metastases was 78.8% versus 42.2%, respectively (P = 0.037). The long-course RT was associated with better 3-year OS compared with short-course (76.4% vs 44.1%, P = 0.03). A total of 15 (83.3%, 15/18) patients achieved pain relief. No grade 3 toxicity was observed. Long-course RT combined with ADT was effective and well-tolerated in PCa patients with bone oligometastases after curative RT for PCa. Further randomized controlled trials are needed to corroborate the findings. Wolters Kluwer Health 2016-02-12 /pmc/articles/PMC4753934/ /pubmed/26871838 http://dx.doi.org/10.1097/MD.0000000000002789 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 |
spellingShingle | 5700 Wu, Jun-Xin Lin, Li-Mei He, Jun-Yan Hong, Liang Li, Jin-Luan Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study |
title | Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study |
title_full | Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study |
title_fullStr | Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study |
title_full_unstemmed | Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study |
title_short | Radiotherapy Combined With Androgen Deprivation for Bone Oligometastases After Primary Curative Radiotherapy for Prostate Cancer: A Retrospective Study |
title_sort | radiotherapy combined with androgen deprivation for bone oligometastases after primary curative radiotherapy for prostate cancer: a retrospective study |
topic | 5700 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753934/ https://www.ncbi.nlm.nih.gov/pubmed/26871838 http://dx.doi.org/10.1097/MD.0000000000002789 |
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