High dose rate brachytherapy boost for prostate cancer: Biochemical control and the impact of transurethral resection of the prostate and hydrogel spacer insertion on toxicity outcomes.
Aged
Aged, 80 and over
Australia
Biomarkers, Tumor
/ blood
Brachytherapy
/ methods
Dose Fractionation, Radiation
Humans
Hydrogels
Male
Middle Aged
Prostatic Neoplasms
/ radiotherapy
Prostheses and Implants
Radiation Injuries
/ prevention & control
Radiotherapy Dosage
Radiotherapy Planning, Computer-Assisted
/ methods
Retrospective Studies
Survival Rate
Tomography, X-Ray Computed
Transurethral Resection of Prostate
TURP
HDR brachytherapy
hydrogel spacers
prostate
Journal
Journal of medical imaging and radiation oncology
ISSN: 1754-9485
Titre abrégé: J Med Imaging Radiat Oncol
Pays: Australia
ID NLM: 101469340
Informations de publication
Date de publication:
Jun 2019
Jun 2019
Historique:
received:
27
10
2018
accepted:
05
03
2019
pubmed:
26
3
2019
medline:
24
12
2019
entrez:
26
3
2019
Statut:
ppublish
Résumé
To examine the long-term outcomes of high dose rate brachytherapy boost (HDR-BT) combined with external beam radiotherapy (EBRT) for intermediate and high-risk prostate cancer patients. Data from 95 patients who underwent combined EBRT (50.4 Gy) and HDR-BT to the prostate between 2010 and 2017 were retrospectively analysed. Biochemical progression free survival (bPFS), local recurrence free survival (LRFS), metastatic free survival (MFS) and overall survival (OS) were estimated using Kaplan-Meier method. Regression analysis was conducted to identify important predictors of outcomes. A total of 24 patients received an initial HDR-BT dose of 18 Gy in three fractions, with the remaining 71 patients receiving 16 Gy in two fractions as per departmental protocol changes. Most patients (88%) received androgen deprivation therapy. A transurethral resection of the prostate (TURP) was performed in 14 patients and hydrogel spacers (HS) were used in 30 patients. Median follow-up was 58 months. The 5-year bPFS, LRFS, MFS and OS were 92%, 100%, 92% and 88%. Univariate regression revealed no statistical association between patient characteristics and time to relapse (all P > 0.1). Late > grade 2 genitourinary (GU) toxicity was 6.3%. The use of HS or prior TURP had no impact on late GU toxicity. Late Grade 1 gastrointestinal (GI) toxicity was 5.3%. The combined HDR-BT with EBRT resulted in excellent bPFS. The cumulative risk of late GU and GI toxicity was low and can be further improved with preventative strategies such as a pre-emptive TURP and/or HS insertion.
Identifiants
pubmed: 30908894
doi: 10.1111/1754-9485.12882
doi:
Substances chimiques
Biomarkers, Tumor
0
Hydrogels
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
415-421Informations de copyright
© 2019 The Royal Australian and New Zealand College of Radiologists.