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Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer

PURPOSE: Stereotactic ablative radiation (SAbR) has been increasingly used in prostate cancer (PCa) given its convenience and cost efficacy. Optimal doses remain poorly defined with limited prospective comparative trials and long-term safety/efficacy data at higher dose levels. We analyzed toxicity...

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Autores principales: Chen, Lily, Gannavarapu, Bhavani S., Desai, Neil B., Folkert, Michael R., Dohopolski, Michael, Gao, Ang, Ahn, Chul, Cadeddu, Jeffrey, Bagrodia, Aditya, Woldu, Solomon, Raj, Ganesh V., Roehrborn, Claus, Lotan, Yair, Timmerman, Robert D., Garant, Aurelie, Hannan, Raquibul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899031/
https://www.ncbi.nlm.nih.gov/pubmed/35265519
http://dx.doi.org/10.3389/fonc.2022.779182
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author Chen, Lily
Gannavarapu, Bhavani S.
Desai, Neil B.
Folkert, Michael R.
Dohopolski, Michael
Gao, Ang
Ahn, Chul
Cadeddu, Jeffrey
Bagrodia, Aditya
Woldu, Solomon
Raj, Ganesh V.
Roehrborn, Claus
Lotan, Yair
Timmerman, Robert D.
Garant, Aurelie
Hannan, Raquibul
author_facet Chen, Lily
Gannavarapu, Bhavani S.
Desai, Neil B.
Folkert, Michael R.
Dohopolski, Michael
Gao, Ang
Ahn, Chul
Cadeddu, Jeffrey
Bagrodia, Aditya
Woldu, Solomon
Raj, Ganesh V.
Roehrborn, Claus
Lotan, Yair
Timmerman, Robert D.
Garant, Aurelie
Hannan, Raquibul
author_sort Chen, Lily
collection PubMed
description PURPOSE: Stereotactic ablative radiation (SAbR) has been increasingly used in prostate cancer (PCa) given its convenience and cost efficacy. Optimal doses remain poorly defined with limited prospective comparative trials and long-term safety/efficacy data at higher dose levels. We analyzed toxicity and outcomes for SAbR in men with localized PCa at escalated 45 Gy in 5 fractions. METHODS AND MATERIALS: This study retrospectively analyzed men from 2015 to 2019 with PCa who received linear-accelerator-based SAbR to 45 Gy in 5 fractions, along with perirectal hydrogel spacer, fiducial placement, and MRI-based planning. Disease control outcomes were calculated from end of treatment. Minimally important difference (MID) assessing patient-reported quality of life was defined as greater than a one-half standard deviation increase in American Urological Association (AUA) symptom score after SAbR. RESULTS: Two-hundred and forty-nine (249) low-, intermediate-, and high-risk PCa patients with median follow-up of 14.9 months for clinical toxicity were included. Acute urinary grade II toxicity occurred in 20.4% of patients. Acute grade II GI toxicity occurred in 7.3% of patients. For follow-up > 2 years (n = 69), late GU and GI grade ≥III toxicity occurred in 5.8% and 1.5% of patients, respectively. MID was evident in 31.8%, 23.4%, 35.8%, 37.0%, 33.3%, and 26.7% of patients at 3, 6, 12, 24, 36, and 48 months, respectively. The median follow-up for biochemical recurrence was 22.6 months with biochemical failure-free survival of 100% at 1 year (n = 226) and 98.7% for years 2 (n = 113) and 3 (n = 54). CONCLUSIONS: SAbR for PCa at 45 Gy in 5 fractions shows an encouraging safety profile. Prospective studies with longer follow-up are warranted to establish this dose regimen as standard of care for PCa.
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spelling pubmed-88990312022-03-08 Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer Chen, Lily Gannavarapu, Bhavani S. Desai, Neil B. Folkert, Michael R. Dohopolski, Michael Gao, Ang Ahn, Chul Cadeddu, Jeffrey Bagrodia, Aditya Woldu, Solomon Raj, Ganesh V. Roehrborn, Claus Lotan, Yair Timmerman, Robert D. Garant, Aurelie Hannan, Raquibul Front Oncol Oncology PURPOSE: Stereotactic ablative radiation (SAbR) has been increasingly used in prostate cancer (PCa) given its convenience and cost efficacy. Optimal doses remain poorly defined with limited prospective comparative trials and long-term safety/efficacy data at higher dose levels. We analyzed toxicity and outcomes for SAbR in men with localized PCa at escalated 45 Gy in 5 fractions. METHODS AND MATERIALS: This study retrospectively analyzed men from 2015 to 2019 with PCa who received linear-accelerator-based SAbR to 45 Gy in 5 fractions, along with perirectal hydrogel spacer, fiducial placement, and MRI-based planning. Disease control outcomes were calculated from end of treatment. Minimally important difference (MID) assessing patient-reported quality of life was defined as greater than a one-half standard deviation increase in American Urological Association (AUA) symptom score after SAbR. RESULTS: Two-hundred and forty-nine (249) low-, intermediate-, and high-risk PCa patients with median follow-up of 14.9 months for clinical toxicity were included. Acute urinary grade II toxicity occurred in 20.4% of patients. Acute grade II GI toxicity occurred in 7.3% of patients. For follow-up > 2 years (n = 69), late GU and GI grade ≥III toxicity occurred in 5.8% and 1.5% of patients, respectively. MID was evident in 31.8%, 23.4%, 35.8%, 37.0%, 33.3%, and 26.7% of patients at 3, 6, 12, 24, 36, and 48 months, respectively. The median follow-up for biochemical recurrence was 22.6 months with biochemical failure-free survival of 100% at 1 year (n = 226) and 98.7% for years 2 (n = 113) and 3 (n = 54). CONCLUSIONS: SAbR for PCa at 45 Gy in 5 fractions shows an encouraging safety profile. Prospective studies with longer follow-up are warranted to establish this dose regimen as standard of care for PCa. Frontiers Media S.A. 2022-02-21 /pmc/articles/PMC8899031/ /pubmed/35265519 http://dx.doi.org/10.3389/fonc.2022.779182 Text en Copyright © 2022 Chen, Gannavarapu, Desai, Folkert, Dohopolski, Gao, Ahn, Cadeddu, Bagrodia, Woldu, Raj, Roehrborn, Lotan, Timmerman, Garant and Hannan https://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) and the copyright owner(s) 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
Chen, Lily
Gannavarapu, Bhavani S.
Desai, Neil B.
Folkert, Michael R.
Dohopolski, Michael
Gao, Ang
Ahn, Chul
Cadeddu, Jeffrey
Bagrodia, Aditya
Woldu, Solomon
Raj, Ganesh V.
Roehrborn, Claus
Lotan, Yair
Timmerman, Robert D.
Garant, Aurelie
Hannan, Raquibul
Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
title Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
title_full Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
title_fullStr Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
title_full_unstemmed Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
title_short Dose-Intensified Stereotactic Ablative Radiation for Localized Prostate Cancer
title_sort dose-intensified stereotactic ablative radiation for localized prostate cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899031/
https://www.ncbi.nlm.nih.gov/pubmed/35265519
http://dx.doi.org/10.3389/fonc.2022.779182
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