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Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial

BACKGROUND: Whether the addition of radiation therapy (RT) improves overall survival in men with locally advanced prostate cancer managed with androgen deprivation therapy (ADT) is unclear. Our aim was to compare outcomes in such patients with locally advanced prostate cancer. METHODS: Patients with...

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Autores principales: Warde, Padraig, Mason, Malcolm, Ding, Keyue, Kirkbride, Peter, Brundage, Michael, Cowan, Richard, Gospodarowicz, Mary, Sanders, Karen, Kostashuk, Edmund, Swanson, Greg, Barber, Jim, Hiltz, Andrea, Parmar, Mahesh KB, Sathya, Jinka, Anderson, John, Hayter, Charles, Hetherington, John, Sydes, Matthew R, Parulekar, Wendy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lancet Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243932/
https://www.ncbi.nlm.nih.gov/pubmed/22056152
http://dx.doi.org/10.1016/S0140-6736(11)61095-7
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author Warde, Padraig
Mason, Malcolm
Ding, Keyue
Kirkbride, Peter
Brundage, Michael
Cowan, Richard
Gospodarowicz, Mary
Sanders, Karen
Kostashuk, Edmund
Swanson, Greg
Barber, Jim
Hiltz, Andrea
Parmar, Mahesh KB
Sathya, Jinka
Anderson, John
Hayter, Charles
Hetherington, John
Sydes, Matthew R
Parulekar, Wendy
author_facet Warde, Padraig
Mason, Malcolm
Ding, Keyue
Kirkbride, Peter
Brundage, Michael
Cowan, Richard
Gospodarowicz, Mary
Sanders, Karen
Kostashuk, Edmund
Swanson, Greg
Barber, Jim
Hiltz, Andrea
Parmar, Mahesh KB
Sathya, Jinka
Anderson, John
Hayter, Charles
Hetherington, John
Sydes, Matthew R
Parulekar, Wendy
author_sort Warde, Padraig
collection PubMed
description BACKGROUND: Whether the addition of radiation therapy (RT) improves overall survival in men with locally advanced prostate cancer managed with androgen deprivation therapy (ADT) is unclear. Our aim was to compare outcomes in such patients with locally advanced prostate cancer. METHODS: Patients with: locally advanced (T3 or T4) prostate cancer (n=1057); or organ-confined disease (T2) with either a prostate-specific antigen (PSA) concentration more than 40 ng/mL (n=119) or PSA concentration more than 20 ng/mL and a Gleason score of 8 or higher (n=25), were randomly assigned (done centrally with stratification and dynamic minimisation, not masked) to receive lifelong ADT and RT (65–69 Gy to the prostate and seminal vesicles, 45 Gy to the pelvic nodes). The primary endpoint was overall survival. The results presented here are of an interim analysis planned for when two-thirds of the events for the final analysis were recorded. All efficacy analyses were done by intention to treat and were based on data from all patients. This trial is registered at controlledtrials.com as ISRCTN24991896 and Clinicaltrials.gov as NCT00002633. RESULTS: Between 1995 and 2005, 1205 patients were randomly assigned (602 in the ADT only group and 603 in the ADT and RT group); median follow-up was 6·0 years (IQR 4·4–8·0). At the time of analysis, a total of 320 patients had died, 175 in the ADT only group and 145 in the ADT and RT group. The addition of RT to ADT improved overall survival at 7 years (74%, 95% CI 70–78 vs 66%, 60–70; hazard ratio [HR] 0·77, 95% CI 0·61–0·98, p=0·033). Both toxicity and health-related quality-of-life results showed a small effect of RT on late gastrointestinal toxicity (rectal bleeding grade >3, three patients (0·5%) in the ADT only group, two (0·3%) in the ADT and RT group; diarrhoea grade >3, four patients (0·7%) vs eight (1·3%); urinary toxicity grade >3, 14 patients (2·3%) in both groups). INTERPRETATION: The benefits of combined modality treatment—ADT and RT—should be discussed with all patients with locally advanced prostate cancer. FUNDING: Canadian Cancer Society Research Institute, US National Cancer Institute, and UK Medical Research Council.
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spelling pubmed-32439322011-12-28 Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial Warde, Padraig Mason, Malcolm Ding, Keyue Kirkbride, Peter Brundage, Michael Cowan, Richard Gospodarowicz, Mary Sanders, Karen Kostashuk, Edmund Swanson, Greg Barber, Jim Hiltz, Andrea Parmar, Mahesh KB Sathya, Jinka Anderson, John Hayter, Charles Hetherington, John Sydes, Matthew R Parulekar, Wendy Lancet Articles BACKGROUND: Whether the addition of radiation therapy (RT) improves overall survival in men with locally advanced prostate cancer managed with androgen deprivation therapy (ADT) is unclear. Our aim was to compare outcomes in such patients with locally advanced prostate cancer. METHODS: Patients with: locally advanced (T3 or T4) prostate cancer (n=1057); or organ-confined disease (T2) with either a prostate-specific antigen (PSA) concentration more than 40 ng/mL (n=119) or PSA concentration more than 20 ng/mL and a Gleason score of 8 or higher (n=25), were randomly assigned (done centrally with stratification and dynamic minimisation, not masked) to receive lifelong ADT and RT (65–69 Gy to the prostate and seminal vesicles, 45 Gy to the pelvic nodes). The primary endpoint was overall survival. The results presented here are of an interim analysis planned for when two-thirds of the events for the final analysis were recorded. All efficacy analyses were done by intention to treat and were based on data from all patients. This trial is registered at controlledtrials.com as ISRCTN24991896 and Clinicaltrials.gov as NCT00002633. RESULTS: Between 1995 and 2005, 1205 patients were randomly assigned (602 in the ADT only group and 603 in the ADT and RT group); median follow-up was 6·0 years (IQR 4·4–8·0). At the time of analysis, a total of 320 patients had died, 175 in the ADT only group and 145 in the ADT and RT group. The addition of RT to ADT improved overall survival at 7 years (74%, 95% CI 70–78 vs 66%, 60–70; hazard ratio [HR] 0·77, 95% CI 0·61–0·98, p=0·033). Both toxicity and health-related quality-of-life results showed a small effect of RT on late gastrointestinal toxicity (rectal bleeding grade >3, three patients (0·5%) in the ADT only group, two (0·3%) in the ADT and RT group; diarrhoea grade >3, four patients (0·7%) vs eight (1·3%); urinary toxicity grade >3, 14 patients (2·3%) in both groups). INTERPRETATION: The benefits of combined modality treatment—ADT and RT—should be discussed with all patients with locally advanced prostate cancer. FUNDING: Canadian Cancer Society Research Institute, US National Cancer Institute, and UK Medical Research Council. Lancet Publishing Group 2011-12-17 /pmc/articles/PMC3243932/ /pubmed/22056152 http://dx.doi.org/10.1016/S0140-6736(11)61095-7 Text en © 2011 Elsevier Ltd. All rights reserved. This document may be redistributed and reused, subject to certain conditions (http://www.elsevier.com/wps/find/authorsview.authors/supplementalterms1.0) .
spellingShingle Articles
Warde, Padraig
Mason, Malcolm
Ding, Keyue
Kirkbride, Peter
Brundage, Michael
Cowan, Richard
Gospodarowicz, Mary
Sanders, Karen
Kostashuk, Edmund
Swanson, Greg
Barber, Jim
Hiltz, Andrea
Parmar, Mahesh KB
Sathya, Jinka
Anderson, John
Hayter, Charles
Hetherington, John
Sydes, Matthew R
Parulekar, Wendy
Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
title Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
title_full Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
title_fullStr Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
title_full_unstemmed Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
title_short Combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
title_sort combined androgen deprivation therapy and radiation therapy for locally advanced prostate cancer: a randomised, phase 3 trial
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243932/
https://www.ncbi.nlm.nih.gov/pubmed/22056152
http://dx.doi.org/10.1016/S0140-6736(11)61095-7
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