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Stereotactic body radiation therapy for the primary treatment of localized prostate cancer
OBJECTIVE: The low alpha/beta ratio of prostate cancer suggests that hypofractionated schemes of dose-escalated radiotherapy should be advantageous. We report our experience using stereotactic body radiation therapy (SBRT) for the primary treatment of prostate cancer to assess efficacy and toxicity....
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3594824/ https://www.ncbi.nlm.nih.gov/pubmed/23504305 http://dx.doi.org/10.1007/s13566-012-0067-2 |
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author | Oliai, Caspian Lanciano, Rachelle Sprandio, Brian Yang, Jun Lamond, John Arrigo, Steven Good, Michael Mooreville, Michael Garber, Bruce Brady, Luther W. |
author_facet | Oliai, Caspian Lanciano, Rachelle Sprandio, Brian Yang, Jun Lamond, John Arrigo, Steven Good, Michael Mooreville, Michael Garber, Bruce Brady, Luther W. |
author_sort | Oliai, Caspian |
collection | PubMed |
description | OBJECTIVE: The low alpha/beta ratio of prostate cancer suggests that hypofractionated schemes of dose-escalated radiotherapy should be advantageous. We report our experience using stereotactic body radiation therapy (SBRT) for the primary treatment of prostate cancer to assess efficacy and toxicity. METHODS: From 2007 to 2010, 70 patients (51 % low risk, 31 % intermediate risk, and 17 % high risk) with localized prostate cancer were treated with SBRT using the CyberKnife system. One-third of patients received androgen deprivation therapy. Doses of 37.5 Gy (n = 29), 36.25 Gy (n = 36), and 35 Gy (n = 5) were administered in five fractions and analyzed as high dose (37.5 Gy) vs. low dose (36.25 and 35 Gy). RESULTS: At a median 27 and 37 months follow-up, the low and high dose groups' median PSA nadir to date was 0.3 and 0.2 ng/ml, respectively. The 3-year freedom from biochemical failure (FFBF) was 100 %, 95.0 % and 77.1 % for the low-, intermediate- and high-risk patients. A dose response was observed in intermediate- and high-risk patients with 72 % vs. 100 % 3-year FFBF for the low and high dose groups, respectively (p = 0.0363). Grade III genitourinary toxicities included 4 % acute and 3 % late (all high dose). Potency was preserved in 83 % of hormone naïve patients. CONCLUSION: CyberKnife dose escalated SBRT for low-, intermediate- and high-risk prostate cancer exhibits favorable efficacy with acceptable toxicity. |
format | Online Article Text |
id | pubmed-3594824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-35948242013-03-14 Stereotactic body radiation therapy for the primary treatment of localized prostate cancer Oliai, Caspian Lanciano, Rachelle Sprandio, Brian Yang, Jun Lamond, John Arrigo, Steven Good, Michael Mooreville, Michael Garber, Bruce Brady, Luther W. J Radiat Oncol Original Research OBJECTIVE: The low alpha/beta ratio of prostate cancer suggests that hypofractionated schemes of dose-escalated radiotherapy should be advantageous. We report our experience using stereotactic body radiation therapy (SBRT) for the primary treatment of prostate cancer to assess efficacy and toxicity. METHODS: From 2007 to 2010, 70 patients (51 % low risk, 31 % intermediate risk, and 17 % high risk) with localized prostate cancer were treated with SBRT using the CyberKnife system. One-third of patients received androgen deprivation therapy. Doses of 37.5 Gy (n = 29), 36.25 Gy (n = 36), and 35 Gy (n = 5) were administered in five fractions and analyzed as high dose (37.5 Gy) vs. low dose (36.25 and 35 Gy). RESULTS: At a median 27 and 37 months follow-up, the low and high dose groups' median PSA nadir to date was 0.3 and 0.2 ng/ml, respectively. The 3-year freedom from biochemical failure (FFBF) was 100 %, 95.0 % and 77.1 % for the low-, intermediate- and high-risk patients. A dose response was observed in intermediate- and high-risk patients with 72 % vs. 100 % 3-year FFBF for the low and high dose groups, respectively (p = 0.0363). Grade III genitourinary toxicities included 4 % acute and 3 % late (all high dose). Potency was preserved in 83 % of hormone naïve patients. CONCLUSION: CyberKnife dose escalated SBRT for low-, intermediate- and high-risk prostate cancer exhibits favorable efficacy with acceptable toxicity. Springer-Verlag 2012-09-12 2013 /pmc/articles/PMC3594824/ /pubmed/23504305 http://dx.doi.org/10.1007/s13566-012-0067-2 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Research Oliai, Caspian Lanciano, Rachelle Sprandio, Brian Yang, Jun Lamond, John Arrigo, Steven Good, Michael Mooreville, Michael Garber, Bruce Brady, Luther W. Stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
title | Stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
title_full | Stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
title_fullStr | Stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
title_full_unstemmed | Stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
title_short | Stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
title_sort | stereotactic body radiation therapy for the primary treatment of localized prostate cancer |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3594824/ https://www.ncbi.nlm.nih.gov/pubmed/23504305 http://dx.doi.org/10.1007/s13566-012-0067-2 |
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