Literature DB >> 26163088

Dosimetry, clinical factors and medication intake influencing urinary symptoms after prostate radiotherapy: An analysis of data from the RADAR prostate radiotherapy trial.

Noorazrul Yahya1, Martin A Ebert2, Max Bulsara3, Annette Haworth4, Angel Kennedy5, David J Joseph6, Jim W Denham7.   

Abstract

PURPOSE/
OBJECTIVE: To identify dosimetry, clinical factors and medication intake impacting urinary symptoms after prostate radiotherapy.
MATERIAL AND METHODS: Data describing clinical factors and bladder dosimetry (reduced with principal component (PC) analysis) for 754 patients treated with external beam radiotherapy accrued by TROG 03.04 RADAR prostate radiotherapy trial were available for analysis. Urinary symptoms (frequency, incontinence, dysuria and haematuria) were prospectively assessed using LENT-SOMA to a median of 72months. The endpoints assessed were prevalence (grade ⩾1) at the end of radiotherapy (representing acute symptoms), at 18-, 36- and 54-month follow-ups (representing late symptoms) and peak late incidence including only grade ⩾2. Impact of factors was assessed using multivariate logistic regression models with correction for over-optimism.
RESULTS: Baseline symptoms, non-insulin dependent diabetes mellitus, age and PC1 (correlated to the mean dose) impact symptoms at >1 timepoints. Associations at a single timepoint were found for cerebrovascular condition, ECOG status and non-steroidal anti-inflammatory drug intake. Peak incidence analysis shows the impact of baseline, bowel and cerebrovascular condition and smoking status.
CONCLUSIONS: The prevalence and incidence analysis provide a complementary view for urinary symptom prediction. Sustained impacts across time points were found for several factors while some associations were not repeated at different time points suggesting poorer or transient impact.
Copyright © 2015 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Prostate cancer; Radiotherapy; Urinary symptoms

Mesh:

Year:  2015        PMID: 26163088     DOI: 10.1016/j.radonc.2015.06.011

Source DB:  PubMed          Journal:  Radiother Oncol        ISSN: 0167-8140            Impact factor:   6.280


  5 in total

1.  Machine Learning on a Genome-wide Association Study to Predict Late Genitourinary Toxicity After Prostate Radiation Therapy.

Authors:  Sangkyu Lee; Sarah Kerns; Harry Ostrer; Barry Rosenstein; Joseph O Deasy; Jung Hun Oh
Journal:  Int J Radiat Oncol Biol Phys       Date:  2018-01-31       Impact factor: 7.038

2.  Volumetric image-guided conformal radiotherapy for localized prostate cancer: Analysis of dosimetric and clinical factors affecting acute and late toxicity.

Authors:  Gianluca Ingrosso; Alessandra Carosi; Daniela di Cristino; Elisabetta Ponti; Andrea Lancia; Marta Bottero; Alessandro Cancelli; Alessandra Murgia; Irene Turturici; Riccardo Santoni
Journal:  Rep Pract Oncol Radiother       Date:  2018-08-13

3.  Incidence of genitourinary complications following radiation therapy for localised prostate cancer.

Authors:  Rowan V David; Arman A Kahokehr; Jason Lee; David I Watson; John Leung; Michael E O'Callaghan
Journal:  World J Urol       Date:  2022-08-11       Impact factor: 3.661

4.  Urinary toxicity after salvage re-irradiation for prostate cancer local failure after definitive radiotherapy: a clinical and dosimetric prognostic factors analysis.

Authors:  Giovanna Dipasquale; Thomas Zilli; Claudio Fiorino; Vérane Achard; Michel Rouzaud; Raymond Miralbell
Journal:  J Contemp Brachytherapy       Date:  2022-06-14

5.  Increased Dose to Organs in Urinary Tract Associates With Measures of Genitourinary Toxicity in Pooled Voxel-Based Analysis of 3 Randomized Phase III Trials.

Authors:  Marco Marcello; James W Denham; Angel Kennedy; Annette Haworth; Allison Steigler; Peter B Greer; Lois C Holloway; Jason A Dowling; Michael G Jameson; Dale Roach; David J Joseph; Sarah L Gulliford; David P Dearnaley; Matthew R Sydes; Emma Hall; Martin A Ebert
Journal:  Front Oncol       Date:  2020-07-22       Impact factor: 6.244

  5 in total

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