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Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study

Objectives: Stereotactic body radiation therapy (SBRT) yields excellent disease control for low- and intermediate-risk prostate cancer by delivering high doses of radiation in a small number of fractions. Our report presents a 7-year update on treatment toxicity and quality of life (QOL) from 515 pa...

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Autores principales: Katz, Alan Jay, Kang, Josephine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211385/
https://www.ncbi.nlm.nih.gov/pubmed/25389521
http://dx.doi.org/10.3389/fonc.2014.00301
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author Katz, Alan Jay
Kang, Josephine
author_facet Katz, Alan Jay
Kang, Josephine
author_sort Katz, Alan Jay
collection PubMed
description Objectives: Stereotactic body radiation therapy (SBRT) yields excellent disease control for low- and intermediate-risk prostate cancer by delivering high doses of radiation in a small number of fractions. Our report presents a 7-year update on treatment toxicity and quality of life (QOL) from 515 patients treated with prostate SBRT. Methods: From 2006 to 2009, 515 patients with clinically localized, low-, intermediate-, and high-risk prostate cancer were treated with SBRT using Cyberknife technology. Treatment consisted of 35–36.25 Gy in 5 fractions. Seventy-two patients received hormone therapy. Toxicity was assessed at each follow-up visit using the expanded prostate cancer index composite (EPIC) questionnaire and the radiation therapy oncology group urinary and rectal toxicity scale. Results: Median follow-up was 72 months. The actuarial 7-year freedom from biochemical failure was 95.8, 89.3, and 68.5% for low-, intermediate-, and high-risk groups, respectively (p < 0.001). No patients experienced acute Grade 3 or 4 acute complications. Fewer than 5% of patients had any acute Grade 2 urinary or rectal toxicity. Late toxicity was low, with Grade 2 rectal and urinary toxicity of 4 and 9.1%, respectively, and Grade 3 urinary toxicity of 1.7%. Mean EPIC urinary and bowel QOL declined at 1 month post-treatment, returned to baseline by 2 years and remained stable thereafter. EPIC sexual QOL declined by 23% at 6–12 months and remained stable afterwards. Of patients potent at baseline evaluation, 67% remained potent at last follow-up. Conclusion: This study suggests that SBRT, when administered to doses of 35–36.25 Gy, is efficacious and safe. With long-term follow-up in our large patient cohort, we continue to find low rates of late toxicity and excellent rates of biochemical control.
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spelling pubmed-42113852014-11-11 Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study Katz, Alan Jay Kang, Josephine Front Oncol Oncology Objectives: Stereotactic body radiation therapy (SBRT) yields excellent disease control for low- and intermediate-risk prostate cancer by delivering high doses of radiation in a small number of fractions. Our report presents a 7-year update on treatment toxicity and quality of life (QOL) from 515 patients treated with prostate SBRT. Methods: From 2006 to 2009, 515 patients with clinically localized, low-, intermediate-, and high-risk prostate cancer were treated with SBRT using Cyberknife technology. Treatment consisted of 35–36.25 Gy in 5 fractions. Seventy-two patients received hormone therapy. Toxicity was assessed at each follow-up visit using the expanded prostate cancer index composite (EPIC) questionnaire and the radiation therapy oncology group urinary and rectal toxicity scale. Results: Median follow-up was 72 months. The actuarial 7-year freedom from biochemical failure was 95.8, 89.3, and 68.5% for low-, intermediate-, and high-risk groups, respectively (p < 0.001). No patients experienced acute Grade 3 or 4 acute complications. Fewer than 5% of patients had any acute Grade 2 urinary or rectal toxicity. Late toxicity was low, with Grade 2 rectal and urinary toxicity of 4 and 9.1%, respectively, and Grade 3 urinary toxicity of 1.7%. Mean EPIC urinary and bowel QOL declined at 1 month post-treatment, returned to baseline by 2 years and remained stable thereafter. EPIC sexual QOL declined by 23% at 6–12 months and remained stable afterwards. Of patients potent at baseline evaluation, 67% remained potent at last follow-up. Conclusion: This study suggests that SBRT, when administered to doses of 35–36.25 Gy, is efficacious and safe. With long-term follow-up in our large patient cohort, we continue to find low rates of late toxicity and excellent rates of biochemical control. Frontiers Media S.A. 2014-10-28 /pmc/articles/PMC4211385/ /pubmed/25389521 http://dx.doi.org/10.3389/fonc.2014.00301 Text en Copyright © 2014 Katz and Kang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Katz, Alan Jay
Kang, Josephine
Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study
title Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study
title_full Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study
title_fullStr Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study
title_full_unstemmed Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study
title_short Quality of Life and Toxicity after SBRT for Organ-Confined Prostate Cancer, a 7-Year Study
title_sort quality of life and toxicity after sbrt for organ-confined prostate cancer, a 7-year study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211385/
https://www.ncbi.nlm.nih.gov/pubmed/25389521
http://dx.doi.org/10.3389/fonc.2014.00301
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