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A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial

BACKGROUND AND PURPOSE: The treatment of biochemical recurrence (BCR) after prostatectomy is challenging as the site of the recurrence is often undetectable. Our aim was to test a personalised treatment concept for BCR based on PSA kinetics during salvage radiotherapy (SRT) combined with prostate-sp...

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Autores principales: Gunnlaugsson, Adalsteinn, Johannesson, Vilberg, Wieslander, Elinore, Brun, Eva, Bitzen, Ulrika, Ståhl, Olof, Bratt, Ola, Ahlgren, Göran, Ohlsson, Tomas, Kjellén, Elisabeth, Nilsson, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305618/
https://www.ncbi.nlm.nih.gov/pubmed/35873652
http://dx.doi.org/10.1016/j.ctro.2022.07.001
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author Gunnlaugsson, Adalsteinn
Johannesson, Vilberg
Wieslander, Elinore
Brun, Eva
Bitzen, Ulrika
Ståhl, Olof
Bratt, Ola
Ahlgren, Göran
Ohlsson, Tomas
Kjellén, Elisabeth
Nilsson, Per
author_facet Gunnlaugsson, Adalsteinn
Johannesson, Vilberg
Wieslander, Elinore
Brun, Eva
Bitzen, Ulrika
Ståhl, Olof
Bratt, Ola
Ahlgren, Göran
Ohlsson, Tomas
Kjellén, Elisabeth
Nilsson, Per
author_sort Gunnlaugsson, Adalsteinn
collection PubMed
description BACKGROUND AND PURPOSE: The treatment of biochemical recurrence (BCR) after prostatectomy is challenging as the site of the recurrence is often undetectable. Our aim was to test a personalised treatment concept for BCR based on PSA kinetics during salvage radiotherapy (SRT) combined with prostate-specific membrane antigen positron emission tomography (PSMA-PET). MATERIALS AND METHODS: This phase II trial included 100 patients with BCR. PSMA-PET was performed at baseline. PSA was measured weekly during SRT. Initially, 70 Gy in 35 fractions was prescribed to the prostate bed. Radiotherapy was adapted after 50 Gy. Non-responders (PSA still ≥ 0.15 ng/mL) received sequential lymph node irradiation with a boost to PSMA-PET positive lesions, while responders (PSA < 0.15 ng/mL) continued SRT as planned. PET-findings were only taken into consideration for treatment planning in case of PSA non-response after 50 Gy. RESULTS: Data from 97 patients were eligible for analysis. Thirty-four patients were classified as responders and 63 as non-responders. PSMA-PET was positive in 3 patients (9%) in the responder group and in 22 (35%) in the non-responder group (p = 0.007). The three-year failure-free survival was 94% for responders and 68% for non-responders (median follow-up 38 months). There were no significant differences in physician-reported urinary and bowel toxicity. Patient-reported diarrhoea at end of SRT was more common among non-responders. CONCLUSION: This new personalised treatment concept with intensified SRT based on PSA response demonstrated a high tumour control rate in both responders and non-responders. These results suggest a clinically significant effect with moderate side effects in a patient group with otherwise poor prognosis. PSMA-PET added limited value. The treatment approach is now being evaluated in a phase III trial. Clinical trial registration numbers: NCT02699424&ISRCTN45905321.
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spelling pubmed-93056182022-07-23 A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial Gunnlaugsson, Adalsteinn Johannesson, Vilberg Wieslander, Elinore Brun, Eva Bitzen, Ulrika Ståhl, Olof Bratt, Ola Ahlgren, Göran Ohlsson, Tomas Kjellén, Elisabeth Nilsson, Per Clin Transl Radiat Oncol Original Research Article BACKGROUND AND PURPOSE: The treatment of biochemical recurrence (BCR) after prostatectomy is challenging as the site of the recurrence is often undetectable. Our aim was to test a personalised treatment concept for BCR based on PSA kinetics during salvage radiotherapy (SRT) combined with prostate-specific membrane antigen positron emission tomography (PSMA-PET). MATERIALS AND METHODS: This phase II trial included 100 patients with BCR. PSMA-PET was performed at baseline. PSA was measured weekly during SRT. Initially, 70 Gy in 35 fractions was prescribed to the prostate bed. Radiotherapy was adapted after 50 Gy. Non-responders (PSA still ≥ 0.15 ng/mL) received sequential lymph node irradiation with a boost to PSMA-PET positive lesions, while responders (PSA < 0.15 ng/mL) continued SRT as planned. PET-findings were only taken into consideration for treatment planning in case of PSA non-response after 50 Gy. RESULTS: Data from 97 patients were eligible for analysis. Thirty-four patients were classified as responders and 63 as non-responders. PSMA-PET was positive in 3 patients (9%) in the responder group and in 22 (35%) in the non-responder group (p = 0.007). The three-year failure-free survival was 94% for responders and 68% for non-responders (median follow-up 38 months). There were no significant differences in physician-reported urinary and bowel toxicity. Patient-reported diarrhoea at end of SRT was more common among non-responders. CONCLUSION: This new personalised treatment concept with intensified SRT based on PSA response demonstrated a high tumour control rate in both responders and non-responders. These results suggest a clinically significant effect with moderate side effects in a patient group with otherwise poor prognosis. PSMA-PET added limited value. The treatment approach is now being evaluated in a phase III trial. Clinical trial registration numbers: NCT02699424&ISRCTN45905321. Elsevier 2022-07-05 /pmc/articles/PMC9305618/ /pubmed/35873652 http://dx.doi.org/10.1016/j.ctro.2022.07.001 Text en © 2022 The Authors 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
Gunnlaugsson, Adalsteinn
Johannesson, Vilberg
Wieslander, Elinore
Brun, Eva
Bitzen, Ulrika
Ståhl, Olof
Bratt, Ola
Ahlgren, Göran
Ohlsson, Tomas
Kjellén, Elisabeth
Nilsson, Per
A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial
title A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial
title_full A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial
title_fullStr A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial
title_full_unstemmed A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial
title_short A prospective phase II study of prostate-specific antigen-guided salvage radiotherapy and (68)Ga-PSMA-PET for biochemical relapse after radical prostatectomy – The PROPER 1 trial
title_sort prospective phase ii study of prostate-specific antigen-guided salvage radiotherapy and (68)ga-psma-pet for biochemical relapse after radical prostatectomy – the proper 1 trial
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9305618/
https://www.ncbi.nlm.nih.gov/pubmed/35873652
http://dx.doi.org/10.1016/j.ctro.2022.07.001
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