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Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results
Background: To evaluate outcomes in terms of survival and toxicity in a series of intermediate-risk prostate cancer (PCa) patients treated with hypofractionated radiotherapy (HyRT) + hormonal therapy (HT) with or without image guidance (IGRT) and to investigate the impact of different variables. Met...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410091/ https://www.ncbi.nlm.nih.gov/pubmed/36013023 http://dx.doi.org/10.3390/jcm11164783 |
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author | Valeriani, Maurizio Di Staso, Mario Facondo, Giuseppe Vullo, Gianluca De Sanctis, Vitaliana Gravina, Giovanni Luca di Genesio Pagliuca, Milena Osti, Mattia Falchetto Bonfili, Pierluigi |
author_facet | Valeriani, Maurizio Di Staso, Mario Facondo, Giuseppe Vullo, Gianluca De Sanctis, Vitaliana Gravina, Giovanni Luca di Genesio Pagliuca, Milena Osti, Mattia Falchetto Bonfili, Pierluigi |
author_sort | Valeriani, Maurizio |
collection | PubMed |
description | Background: To evaluate outcomes in terms of survival and toxicity in a series of intermediate-risk prostate cancer (PCa) patients treated with hypofractionated radiotherapy (HyRT) + hormonal therapy (HT) with or without image guidance (IGRT) and to investigate the impact of different variables. Methods: This is a multi-centric study. From January 2005 to December 2019, we treated 313 intermediate-risk PCa patients (T2b–T2c, Gleason score 7, or pre-treatment PSA 10 to 20 ng/mL) with HyRT. Patients received 54.75 Gy in 15 fractions in 5 weeks plus 9 months of neo-adjuvant, concomitant, and adjuvant HT with or without IGRT. Results: Median follow-up was 91.6 months (range 5.1–167.8 months). Median OS was not reached, and the 8- and 10-year OS was 81.9% and 72.4%, respectively. Median CSS was not reached, and the 8- and 10-year CSS was 97.9% and 94.5%, respectively. PSA at first follow-up <0.8 ng/mL was significantly related to better oncological outcomes (CSS, bRFS, LRFS, cPFS, and MFS) in both univariate and multivariate analysis. After Propensity Score matching, grade 2–3 acute and cumulative late GU (p = 0.153 and p = 0.581, respectively) and GI (p = 0.196 and p = 0.925, respectively) toxicity were not statistically different in patients treated with or without IGRT. Conclusions: HyRT is effective and safe regardless of the use of IGRT. PSA at first follow-up is an easily accessible prognostic factor that may help the clinicians to identify patients who require a treatment intensification. |
format | Online Article Text |
id | pubmed-9410091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-94100912022-08-26 Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results Valeriani, Maurizio Di Staso, Mario Facondo, Giuseppe Vullo, Gianluca De Sanctis, Vitaliana Gravina, Giovanni Luca di Genesio Pagliuca, Milena Osti, Mattia Falchetto Bonfili, Pierluigi J Clin Med Article Background: To evaluate outcomes in terms of survival and toxicity in a series of intermediate-risk prostate cancer (PCa) patients treated with hypofractionated radiotherapy (HyRT) + hormonal therapy (HT) with or without image guidance (IGRT) and to investigate the impact of different variables. Methods: This is a multi-centric study. From January 2005 to December 2019, we treated 313 intermediate-risk PCa patients (T2b–T2c, Gleason score 7, or pre-treatment PSA 10 to 20 ng/mL) with HyRT. Patients received 54.75 Gy in 15 fractions in 5 weeks plus 9 months of neo-adjuvant, concomitant, and adjuvant HT with or without IGRT. Results: Median follow-up was 91.6 months (range 5.1–167.8 months). Median OS was not reached, and the 8- and 10-year OS was 81.9% and 72.4%, respectively. Median CSS was not reached, and the 8- and 10-year CSS was 97.9% and 94.5%, respectively. PSA at first follow-up <0.8 ng/mL was significantly related to better oncological outcomes (CSS, bRFS, LRFS, cPFS, and MFS) in both univariate and multivariate analysis. After Propensity Score matching, grade 2–3 acute and cumulative late GU (p = 0.153 and p = 0.581, respectively) and GI (p = 0.196 and p = 0.925, respectively) toxicity were not statistically different in patients treated with or without IGRT. Conclusions: HyRT is effective and safe regardless of the use of IGRT. PSA at first follow-up is an easily accessible prognostic factor that may help the clinicians to identify patients who require a treatment intensification. MDPI 2022-08-16 /pmc/articles/PMC9410091/ /pubmed/36013023 http://dx.doi.org/10.3390/jcm11164783 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Valeriani, Maurizio Di Staso, Mario Facondo, Giuseppe Vullo, Gianluca De Sanctis, Vitaliana Gravina, Giovanni Luca di Genesio Pagliuca, Milena Osti, Mattia Falchetto Bonfili, Pierluigi Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results |
title | Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results |
title_full | Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results |
title_fullStr | Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results |
title_full_unstemmed | Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results |
title_short | Hypofractionated Radiotherapy in Intermediate-Risk Prostate Cancer Patients: Long-Term Results |
title_sort | hypofractionated radiotherapy in intermediate-risk prostate cancer patients: long-term results |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9410091/ https://www.ncbi.nlm.nih.gov/pubmed/36013023 http://dx.doi.org/10.3390/jcm11164783 |
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