Randomised Trial of No, Short-term, or Long-term Androgen Deprivation Therapy with Postoperative Radiotherapy After Radical Prostatectomy: Results from the Three-way Comparison of RADICALS-HD (NCT00541047).

Androgen deprivation therapy Clinical trials Duration Hormone therapy Multiarm trial Prostate cancer Radical prostatectomy Radiotherapy Randomised controlled trial

Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
30 Aug 2024
Historique:
received: 26 03 2024
revised: 31 05 2024
accepted: 29 07 2024
medline: 1 9 2024
pubmed: 1 9 2024
entrez: 31 8 2024
Statut: aheadofprint

Résumé

The use and duration of androgen deprivation therapy (ADT) with postoperative radiotherapy (RT) have been uncertain. RADICALS-HD compared adding no ("None"), 6-months ("Short"), or 24-mo ("Long") ADT to study efficacy in the long term. Participants with prostate cancer were indicated for postoperative RT and agreed randomisation between all durations. ADT was allocated for 0, 6, or 24 mo. The primary outcome measure (OM) was metastasis-free survival (MFS). The secondary OMs included freedom from distant metastasis, overall survival, and initiation of nonprotocol ADT. Sample size was determined by two-way comparisons. Analyses followed standard time-to-event approaches and intention-to-treat principles. Between 2007 and 2015, 492 participants were randomised one of three groups: 166 None, 164 Short, and 162 Long. The median age at randomisation was 66 yr; Gleason scores at surgery were as follows: <7 = 64 (13%), 3+4 = 229 (47%), 4+3 = 127 (26%), and 8+ = 72 (15%); T3b was 112 (23%); and T4 was 5 (1%). The median follow-up was 9.0 yr and, with MFS events reported for 89 participants (32 None, 31 Short, and 26 Long), there was no evidence of difference in MFS overall (logrank p = 0.98), and, for Long versus None, hazard ratio = 0.948 (95% confidence interval 0.54-1.68). After 10 yr, 80% None, 77% Short, and 81% Long patients were alive without metastatic disease. The three-way randomisation was not powered to conventional levels for assessment, yet provides a fair comparison. Long-term outcomes after radical prostatectomy are usually favourable. In those indicated for postoperative RT and considered suitable for no, short-term, or long-term ADT, there was no evidence of improvement with addition of ADT. Future research should focus on patients at a higher risk of metastases in whom improvements are required more urgently.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
The use and duration of androgen deprivation therapy (ADT) with postoperative radiotherapy (RT) have been uncertain. RADICALS-HD compared adding no ("None"), 6-months ("Short"), or 24-mo ("Long") ADT to study efficacy in the long term.
METHODS METHODS
Participants with prostate cancer were indicated for postoperative RT and agreed randomisation between all durations. ADT was allocated for 0, 6, or 24 mo. The primary outcome measure (OM) was metastasis-free survival (MFS). The secondary OMs included freedom from distant metastasis, overall survival, and initiation of nonprotocol ADT. Sample size was determined by two-way comparisons. Analyses followed standard time-to-event approaches and intention-to-treat principles.
KEY FINDINGS AND LIMITATIONS UNASSIGNED
Between 2007 and 2015, 492 participants were randomised one of three groups: 166 None, 164 Short, and 162 Long. The median age at randomisation was 66 yr; Gleason scores at surgery were as follows: <7 = 64 (13%), 3+4 = 229 (47%), 4+3 = 127 (26%), and 8+ = 72 (15%); T3b was 112 (23%); and T4 was 5 (1%). The median follow-up was 9.0 yr and, with MFS events reported for 89 participants (32 None, 31 Short, and 26 Long), there was no evidence of difference in MFS overall (logrank p = 0.98), and, for Long versus None, hazard ratio = 0.948 (95% confidence interval 0.54-1.68). After 10 yr, 80% None, 77% Short, and 81% Long patients were alive without metastatic disease. The three-way randomisation was not powered to conventional levels for assessment, yet provides a fair comparison.
CONCLUSIONS AND CLINICAL IMPLICATIONS CONCLUSIONS
Long-term outcomes after radical prostatectomy are usually favourable. In those indicated for postoperative RT and considered suitable for no, short-term, or long-term ADT, there was no evidence of improvement with addition of ADT. Future research should focus on patients at a higher risk of metastases in whom improvements are required more urgently.

Identifiants

pubmed: 39217077
pii: S0302-2838(24)02515-6
doi: 10.1016/j.eururo.2024.07.026
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Auteurs

Chris C Parker (CC)

Royal Marsden NHS Foundation Trust, Sutton, UK; The Institute of Cancer Research, Sutton, UK.

Noel W Clarke (NW)

Department of Urology, The Christie and Salford Royal Hospitals, Manchester, UK; The University of Manchester, Manchester, UK.

Adrian D Cook (AD)

MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, UCL, London, UK.

Peter M Petersen (PM)

Department of Oncology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.

Charles N Catton (CN)

Department of Radiation Oncology, Princess Margaret, Cancer Centre, University Health Network, Toronto, ON, Canada.

William R Cross (WR)

Department of Urology, St James's University Hospital, Leeds, UK.

Howard Kynaston (H)

Division of Cancer & Genetics, Cardiff University Medical School, Cardiff, UK.

Raj A Persad (RA)

Department of Urology, Bristol Urological Institute, Bristol, UK.

Fred Saad (F)

Department of Urology, Centre Hospitalier de l'Université de Montréal, Montreal, Canada.

John Logue (J)

Christie Hospital, Manchester, UK.

Heather Payne (H)

The Prostate Centre, London, UK.

Claire Amos (C)

MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, UCL, London, UK.

Lorna Bower (L)

The Institute of Cancer Research, Sutton, UK; Guy's and St Thomas' NHS Foundation Trust, London, UK.

Rakesh Raman (R)

Kent Oncology Centre, Kent & Canterbury Hospital, Canterbury, UK.

Ian Sayers (I)

Deanesly Centre, New Cross Hospital, Wolverhampton, UK.

Jane Worlding (J)

University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.

Wendy R Parulekar (WR)

Canadian Cancer Trials Group, Queen's University, Kingston, ON, Canada.

Mahesh K B Parmar (MKB)

MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, UCL, London, UK.

Matthew R Sydes (MR)

MRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, UCL, London, UK. Electronic address: m.sydes@ucl.ac.uk.

Classifications MeSH