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Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer

PURPOSE: To evaluate the oncological outcome after stereotactic body radiation therapy (SBRT) for oligometastatic hormone-sensitive prostate cancer (omHSPC) patients. MATERIALS-METHODS: In this retrospective, observational, multi-institutional study, omHSPC patients (≤5 metastases) underwent SBRT. P...

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Autores principales: Baron, D., Pasquier, D., Pace-Loscos, T., Vandendorpe, B, Schiappa, R., Ortholan, C., Hannoun-Levi, J.M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493250/
https://www.ncbi.nlm.nih.gov/pubmed/37701481
http://dx.doi.org/10.1016/j.ctro.2023.100673
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author Baron, D.
Pasquier, D.
Pace-Loscos, T.
Vandendorpe, B
Schiappa, R.
Ortholan, C.
Hannoun-Levi, J.M.
author_facet Baron, D.
Pasquier, D.
Pace-Loscos, T.
Vandendorpe, B
Schiappa, R.
Ortholan, C.
Hannoun-Levi, J.M.
author_sort Baron, D.
collection PubMed
description PURPOSE: To evaluate the oncological outcome after stereotactic body radiation therapy (SBRT) for oligometastatic hormone-sensitive prostate cancer (omHSPC) patients. MATERIALS-METHODS: In this retrospective, observational, multi-institutional study, omHSPC patients (≤5 metastases) underwent SBRT. Primary endpoint was systemic therapy escalation-free survival (STE-FS) after SBRT. Local (LR), distant (DR), prostatic (PR) and isolated biochemical (iBR) relapses were reported with progression-free survival (PFS) and overall survival (OS). Prognostic factors for STE-FS were investigated. Toxicity was reported. RESULTS: From 01/07 to 09/19, 119 pts with omHSPC underwent SBRT. With a MFU of 34 months [12–97], median STE-FS was 33.4 months (95%CI 26.6–––40.1). Median OS was not reached and PFS was 22.7 months (CI95% 18.6–––32.3). Post-SBRT-PSA remained stable or decreased in 87 pts (73.1%). Progression events (LR, MR, PR, iBR) were observed in 72 pts (60.5%), among whom 6 relapsed in the irradiated area (local control rate: 95%). DR, BR, PR were observed in 44 pts (37%), 21pts (17.7%) and 2 pts (1.7%) respectively. In multivariate analysis, post-SBRT biochemical response was an independent prognostic factor for STE-FS. Grade ≥ 3 toxicity occurred in 1pt. CONCLUSION: With excellent local control and tolerance, SBRT for omHSPC patients represents an attractive approach to defer systemic therapeutic escalation and prevent its side effects. Accurate patient selection for SBRT requires more data with longer follow-up and higher numbers of patients pending the results of upcoming randomized trials.
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spelling pubmed-104932502023-09-12 Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer Baron, D. Pasquier, D. Pace-Loscos, T. Vandendorpe, B Schiappa, R. Ortholan, C. Hannoun-Levi, J.M. Clin Transl Radiat Oncol Original Research Article PURPOSE: To evaluate the oncological outcome after stereotactic body radiation therapy (SBRT) for oligometastatic hormone-sensitive prostate cancer (omHSPC) patients. MATERIALS-METHODS: In this retrospective, observational, multi-institutional study, omHSPC patients (≤5 metastases) underwent SBRT. Primary endpoint was systemic therapy escalation-free survival (STE-FS) after SBRT. Local (LR), distant (DR), prostatic (PR) and isolated biochemical (iBR) relapses were reported with progression-free survival (PFS) and overall survival (OS). Prognostic factors for STE-FS were investigated. Toxicity was reported. RESULTS: From 01/07 to 09/19, 119 pts with omHSPC underwent SBRT. With a MFU of 34 months [12–97], median STE-FS was 33.4 months (95%CI 26.6–––40.1). Median OS was not reached and PFS was 22.7 months (CI95% 18.6–––32.3). Post-SBRT-PSA remained stable or decreased in 87 pts (73.1%). Progression events (LR, MR, PR, iBR) were observed in 72 pts (60.5%), among whom 6 relapsed in the irradiated area (local control rate: 95%). DR, BR, PR were observed in 44 pts (37%), 21pts (17.7%) and 2 pts (1.7%) respectively. In multivariate analysis, post-SBRT biochemical response was an independent prognostic factor for STE-FS. Grade ≥ 3 toxicity occurred in 1pt. CONCLUSION: With excellent local control and tolerance, SBRT for omHSPC patients represents an attractive approach to defer systemic therapeutic escalation and prevent its side effects. Accurate patient selection for SBRT requires more data with longer follow-up and higher numbers of patients pending the results of upcoming randomized trials. Elsevier 2023-08-31 /pmc/articles/PMC10493250/ /pubmed/37701481 http://dx.doi.org/10.1016/j.ctro.2023.100673 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Baron, D.
Pasquier, D.
Pace-Loscos, T.
Vandendorpe, B
Schiappa, R.
Ortholan, C.
Hannoun-Levi, J.M.
Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
title Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
title_full Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
title_fullStr Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
title_full_unstemmed Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
title_short Systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
title_sort systemic therapy escalation after stereotactic body radiation therapy for oligometastatic hormone-sensitive prostate cancer
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493250/
https://www.ncbi.nlm.nih.gov/pubmed/37701481
http://dx.doi.org/10.1016/j.ctro.2023.100673
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