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Biochemical outcome of prostate cancer patients treated with hypofractionated external radiation and a single high-dose-rate brachytherapy boost
Örebro universitet, Institutionen för medicinska vetenskaper. Department of Oncology, General Hospital of Karlstad, Karlstad, Sweden; Department of oncology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Örebro universitet, Institutionen för medicinska vetenskaper. Region Örebro län. Department of Oncology.ORCID-id: 0000-0001-6059-0194
Department of Medical Physics, Örebro University Hospital, Örebro, Sweden.
Örebro universitet, Institutionen för medicinska vetenskaper. Region Örebro län. Department of Oncology.
2025 (engelsk)Inngår i: Brachytherapy, ISSN 1538-4721, E-ISSN 1873-1449, Vol. 24, nr 1, s. 45-53Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

INTRODUCTION: Treating localized high-risk prostate cancer with a combination of external beam radiation therapy (EBRT) and high-dose-rate brachytherapy (HDR-BT) is a common approach. Moderately hypofractionated EBRT and a single HDR-BT boost simplifies the treatment. We aim to present our five-year results.

METHODS: In this study, 355 patients treated with moderately hypofractionated EBRT (42 Gy in 14 fractions) and a single HDR-BT boost (14.5 Gy) at Örebro University Hospital between 2008 and 2018 were included. They were followed with regular PSA tests.

RESULTS: The median age of the cohort was 70 years (range: 51-81) and the median follow-up duration was 56 months (range: 6-150). Among them, 45% were classified as very high-risk, 38% as high-risk and 17% as intermediate-risk. Adjuvant androgen deprivation therapy (ADT) with a median duration of 24 months was given to 75% of the patient cohort. The estimated 5-year failure free survival rates were 79% (whole cohort), 66% (very high-risk), 90% (high-risk) and 85% (intermediate-risk), respectively. Initial PSA > 10 ng/mL, Gleason score 9-10 and tumor stage T3 were significantly associated with biochemical failure (BF). A PSA bounce occurred in 53 (15%) cases and was inversely associated with BF (p = 0.001) for patients receiving ADT.

CONCLUSIONS: Moderately hypofractionated EBRT and a single HDR-BT boost seems to be an effective treatment against intermediate- and high-risk localized prostate cancer. Treatment escalation strategies should be investigated for very high-risk patients where the risk of recurrence remains high.

sted, utgiver, år, opplag, sider
Elsevier, 2025. Vol. 24, nr 1, s. 45-53
Emneord [en]
Boost, Bounce, Brachytherapy, HDR, Prostate cancer, Radiation therapy
HSV kategori
Identifikatorer
URN: urn:nbn:se:oru:diva-117630DOI: 10.1016/j.brachy.2024.07.005ISI: 001402302000001PubMedID: 39578204Scopus ID: 2-s2.0-85210092315OAI: oai:DiVA.org:oru-117630DiVA, id: diva2:1919289
Tilgjengelig fra: 2024-12-09 Laget: 2024-12-09 Sist oppdatert: 2025-01-31bibliografisk kontrollert
Inngår i avhandling
1. Radiotherapy of prostate cancer with aspects on hypofractionation and high precision
Åpne denne publikasjonen i ny fane eller vindu >>Radiotherapy of prostate cancer with aspects on hypofractionation and high precision
2025 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

Hypofractionated radiotherapy (RT), including high dose rate brachy-therapy (HDR-BT) is a theoretically beneficial treatment option for curable prostate cancer. Our studies aimed to contribute to the growing body of results on the effectiveness and safety of HDR-BT both as monotherapy and as a boost in combination with external beam radiation therapy (EBRT).

In paper I, 229 patients (low- and intermediate-risk) received 2 – 4 fractions of HDR-BT as monotherapy. The median follow-up time was 85 months. In total, 9.6% had a biochemical failure (BF) and severe toxicities were uncommon. The treatment was found to be effective and safe.

In paper II, 355 patients (83% classified as high- or very high risk) received EBRT (3 Gy x 14) + a single fraction of HDR-BT (14.5 Gy). The median follow-up time was 56 months. The estimated five-year failure free survival was 79 % for the whole cohort. Our results suggest that this treatment appears to be feasible in terms of efficacy.

In paper III, 34 patients who received EBRT + HDR-BT were randomized to either five or three fractions of EBRT per week. Intrafractional prostate movement was tracked in real-time using the Raypilot® system. The primary endpoint was patient-reported acute toxicity. We found no significant difference between the study groups. Target displacement was less than 2 mm during 97% of the time, supporting the use of small treatment margins.

In paper IV, 175 patients received two fractions of HDR-BT (14 Gy x 2) as monotherapy. The estimated five-year cumulative BF rate was 3% for low-risk patients and 9.6% for intermediate-risk patients. The proportion of severe urinary and bowel toxicities were low, indicating that this treatment approach is effective and safe.

sted, utgiver, år, opplag, sider
Örebro: Örebro University, 2025. s. 73
Serie
Örebro Studies in Medicine, ISSN 1652-4063 ; 309
Emneord
Prostate cancer, radiation therapy, brachytherapy, high dose rate, hypofractionation
HSV kategori
Identifikatorer
urn:nbn:se:oru:diva-117125 (URN)9789175296159 (ISBN)9789175296166 (ISBN)
Disputas
2025-01-10, Örebro universitet, Campus USÖ, hörsal X1, Södra Grev Rosengatan 32, Örebro, 10:00 (svensk)
Opponent
Veileder
Tilgjengelig fra: 2024-10-30 Laget: 2024-10-30 Sist oppdatert: 2025-01-21bibliografisk kontrollert

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