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PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases

BACKGROUND: In the current study we evaluated (68)Ga PSMA PET/ CT to measure local control of bone metastasis in oligometastatic prostate cancer patients treated with SBRT. MATERIALS AND METHODS: After the institutional review board approval, a retrospective review of medical records of consecutive...

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Autores principales: Sadetski, Igor, Eshet, Yael, Kaidar-Person, Orit, Amit, Uri, Domachevsky, Liran, Davidson, Tima, Weiss, Ilana, Ben Ayun, Maoz, Symon, Zvi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Via Medica 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382074/
https://www.ncbi.nlm.nih.gov/pubmed/34434568
http://dx.doi.org/10.5603/RPOR.a2021.0071
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author Sadetski, Igor
Eshet, Yael
Kaidar-Person, Orit
Amit, Uri
Domachevsky, Liran
Davidson, Tima
Weiss, Ilana
Ben Ayun, Maoz
Symon, Zvi
author_facet Sadetski, Igor
Eshet, Yael
Kaidar-Person, Orit
Amit, Uri
Domachevsky, Liran
Davidson, Tima
Weiss, Ilana
Ben Ayun, Maoz
Symon, Zvi
author_sort Sadetski, Igor
collection PubMed
description BACKGROUND: In the current study we evaluated (68)Ga PSMA PET/ CT to measure local control of bone metastasis in oligometastatic prostate cancer patients treated with SBRT. MATERIALS AND METHODS: After the institutional review board approval, a retrospective review of medical records of consecutive prostate cancer patients treated between 2014 and 2018 was conducted. Only medical records of patients that were treated with SBRT for bone metastasis and had pre-and post-SBRT (68)Ga PSMA PET/CT scans were included in our study. Data extracted from the medical files included patient-related (age), disease-related (Gleason score, site of metastasis), and treatment-related factors and outcomes. RESULTS: During the study period, a total of 12 patients (15 lesions) were included, with a median age of 73 years. The median follow-up was 26.5 months (range 13–45 months). Median time of (68)Ga PSMA PET/ CT follow up was 17.0 months (range 3–39 months). The median pre-treatment PSA was 2 ng/mL (range 0.56–44 ng/mL) vs. post treatment PSA nadir of 0.01 ng/mL (0.01–4.32) with a median time to nadir of 7 months (range, 2–12). Local control was 93% during the follow up period and there was correlation with PS MA avidity on PE T. None patients developed recurrences in the treated bone. None of the patients had grade 3 or more toxicities during follow-up. CONCLUSIONS: SBRT is a highly effective and safe method for treatment of prostate cancer bone metastases. More studies are required to determine if SBRT provides greater clinical benefit than standard fractionation for oligometastatic prostate cancer patients. (68)Ga PSMA PET/CT should be further investigated for delineation and follow-up.
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spelling pubmed-83820742021-08-24 PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases Sadetski, Igor Eshet, Yael Kaidar-Person, Orit Amit, Uri Domachevsky, Liran Davidson, Tima Weiss, Ilana Ben Ayun, Maoz Symon, Zvi Rep Pract Oncol Radiother Research Paper BACKGROUND: In the current study we evaluated (68)Ga PSMA PET/ CT to measure local control of bone metastasis in oligometastatic prostate cancer patients treated with SBRT. MATERIALS AND METHODS: After the institutional review board approval, a retrospective review of medical records of consecutive prostate cancer patients treated between 2014 and 2018 was conducted. Only medical records of patients that were treated with SBRT for bone metastasis and had pre-and post-SBRT (68)Ga PSMA PET/CT scans were included in our study. Data extracted from the medical files included patient-related (age), disease-related (Gleason score, site of metastasis), and treatment-related factors and outcomes. RESULTS: During the study period, a total of 12 patients (15 lesions) were included, with a median age of 73 years. The median follow-up was 26.5 months (range 13–45 months). Median time of (68)Ga PSMA PET/ CT follow up was 17.0 months (range 3–39 months). The median pre-treatment PSA was 2 ng/mL (range 0.56–44 ng/mL) vs. post treatment PSA nadir of 0.01 ng/mL (0.01–4.32) with a median time to nadir of 7 months (range, 2–12). Local control was 93% during the follow up period and there was correlation with PS MA avidity on PE T. None patients developed recurrences in the treated bone. None of the patients had grade 3 or more toxicities during follow-up. CONCLUSIONS: SBRT is a highly effective and safe method for treatment of prostate cancer bone metastases. More studies are required to determine if SBRT provides greater clinical benefit than standard fractionation for oligometastatic prostate cancer patients. (68)Ga PSMA PET/CT should be further investigated for delineation and follow-up. Via Medica 2021-08-12 /pmc/articles/PMC8382074/ /pubmed/34434568 http://dx.doi.org/10.5603/RPOR.a2021.0071 Text en © 2021 Greater Poland Cancer Centre https://creativecommons.org/licenses/by-nc-nd/4.0/This article is available in open access under Creative Common Attribution-Non-Commercial-No Derivatives 4.0 International (CC BY-NC-ND 4.0) license, allowing to download articles and share them with others as long as they credit the authors and the publisher, but without permission to change them in any way or use them commercially
spellingShingle Research Paper
Sadetski, Igor
Eshet, Yael
Kaidar-Person, Orit
Amit, Uri
Domachevsky, Liran
Davidson, Tima
Weiss, Ilana
Ben Ayun, Maoz
Symon, Zvi
PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases
title PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases
title_full PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases
title_fullStr PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases
title_full_unstemmed PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases
title_short PSMA PET/CT to evaluate response to SBRT for prostate cancer bone metastases
title_sort psma pet/ct to evaluate response to sbrt for prostate cancer bone metastases
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8382074/
https://www.ncbi.nlm.nih.gov/pubmed/34434568
http://dx.doi.org/10.5603/RPOR.a2021.0071
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