A comparison of outcomes for patients with intermediate and high risk prostate cancer treated with low dose rate and high dose rate brachytherapy in combination with external beam radiotherapy.

External beam radiotherapy High dose rate brachytherapy Low dose rate brachytherapy Prostate cancer

Journal

Clinical and translational radiation oncology
ISSN: 2405-6308
Titre abrégé: Clin Transl Radiat Oncol
Pays: Ireland
ID NLM: 101713416

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 17 09 2019
revised: 08 10 2019
accepted: 09 10 2019
entrez: 9 11 2019
pubmed: 9 11 2019
medline: 9 11 2019
Statut: epublish

Résumé

There is evidence to support use of external beam radiotherapy (EBRT) in combination with both low dose rate brachytherapy (LDR-EBRT) and high dose rate brachytherapy (HDR-EBRT) to treat intermediate and high risk prostate cancer. Men with intermediate and high risk prostate cancer treated using LDR-EBRT (treated between 1996 and 2007) and HDR-EBRT (treated between 2007 and 2012) were identified from an institutional database. Multivariable analysis was performed to evaluate the relationship between patient, disease and treatment factors with biochemical progression free survival (bPFS). 116 men were treated with LDR-EBRT and 171 were treated with HDR-EBRT. At 5 years, bPFS was estimated to be 90.5% for the LDR-EBRT cohort and 77.6% for the HDR-EBRT cohort. On multivariable analysis, patients treated with HDR-EBRT were more than twice as likely to experience biochemical progression compared with LDR-EBRT (HR 2.33, 95% CI 1.12-4.07). Patients with Gleason ≥8 disease were more than five times more likely to experience biochemical progression compared with Gleason 6 disease (HR 5.47, 95% CI 1.26-23.64). Cumulative incidence of ≥grade 3 genitourinary and gastrointestinal toxicities for the LDR-EBRT and HDR-EBRT cohorts were 8% versus 4% and 5% versus 1% respectively, although these differences did not reach statistical significance. LDR-EBRT may provide more effective PSA control at 5 years compared with HDR-EBRT. Direct comparison of these treatments through randomised trials are recommended to investigate this hypothesis further.

Identifiants

pubmed: 31701035
doi: 10.1016/j.ctro.2019.10.001
pii: S2405-6308(19)30101-6
pmc: PMC6831705
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1-8

Informations de copyright

© 2019 The Authors.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

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Auteurs

Finbar Slevin (F)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.
University of Leeds, Leeds LS2 9JT, UK.

Sree Lakshmi Rodda (SL)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Peter Bownes (P)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Louise Murray (L)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.
University of Leeds, Leeds LS2 9JT, UK.

David Bottomley (D)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Clare Wilkinson (C)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Ese Adiotomre (E)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Bashar Al-Qaisieh (B)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Emma Dugdale (E)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Oliver Hulson (O)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Joshua Mason (J)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Jonathan Smith (J)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.

Ann M Henry (AM)

Leeds Teaching Hospitals NHS Trust, Beckett Street, Leeds LS9 7TF, UK.
University of Leeds, Leeds LS2 9JT, UK.

Classifications MeSH