Radiation Dose Escalation or Longer Androgen Suppression to Prevent Distant Progression in Men With Locally Advanced Prostate Cancer: 10-Year Data From the TROG 03.04 RADAR Trial.


Journal

International journal of radiation oncology, biology, physics
ISSN: 1879-355X
Titre abrégé: Int J Radiat Oncol Biol Phys
Pays: United States
ID NLM: 7603616

Informations de publication

Date de publication:
15 03 2020
Historique:
received: 17 11 2019
revised: 17 11 2019
accepted: 21 11 2019
entrez: 25 2 2020
pubmed: 25 2 2020
medline: 21 4 2020
Statut: ppublish

Résumé

To clarify the relative effects of duration of androgen suppression (AS) and radiation dose escalation (RDE) on distant progression (DP) in men with locally advanced prostate cancer. Participants with locally advanced prostate cancer in the TROG 03.04 RADAR trial were randomized to 6 or 18 months AS ± 18 months zoledronic acid (Z). The trial incorporated a RDE program by stratification at randomization and dosing options were 66, 70, or 74 Gy external beam radiation therapy (EBRT), or 46 Gy EBRT plus high-dose-rate brachytherapy boost (HDRB). The primary endpoint for this study was distant progression (DP). Secondary endpoints included local progression, bone progression, prostate cancer-specific mortality and all-cause mortality. Effect estimates for AS duration and RDE were derived using Fine and Gray competing risk models adjusting for use of Z, age, tumor stage, Gleason grade group, prostate-specific antigen, and treatment center. Cumulative incidence at 10 years was estimated for each RDE group. A total of 1051 out of 1071 randomized subjects were eligible for inclusion in this analysis. Compared with 6 months AS, 18 months AS significantly reduced DP independently of radiation dose (subhazard ratio 0.70; 95% confidence interval [CI], 0.56-0.87; P = .002). No statistically significant interaction between effect of AS duration and RT dose was observed (Wald test P = .76). In subgroup analyses, DP was significantly reduced by the longer duration of AS in the 70 Gy and HDRB groups but not in the 66 Gy and 74 Gy. Compared with 70 Gy, HDRB significantly reduced DP (subhazard ratio 0.68 [95% CI, 0.57-0.80]; P < .0001) independently of AS duration. At 10 years, adjusted cumulative incidences were 26.1% (95% CI, 18.9%-33.2%), 26.7% (22.9%-30.6%), 24.9% (20.0%-29.8%) and 19.7% (15.5%-23.8%) for DPs in the respective radiation dose groups. Compared with 6 months AS, 18 months AS reduced DP independently of radiation dose. Men treated with HDRB gained a significant benefit from a longer duration of AS. Evidence of improved oncologic outcomes for HDRB compared with dose-escalated EBRT needs to be confirmed in a randomized trial.

Identifiants

pubmed: 32092343
pii: S0360-3016(19)34518-3
doi: 10.1016/j.ijrobp.2019.11.415
pii:
doi:

Substances chimiques

Androgen Antagonists 0
Androgens 0

Types de publication

Clinical Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

693-702

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

David Joseph (D)

Department of Medicine and Surgery, University of Western Australia, Western Australia, Australia; GenesisCare, Joondalup, Western Australia, Australia; 5D Clinics, Claremont, Western Australia, Australia.

James W Denham (JW)

School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia. Electronic address: Jim.Denham@newcastle.edu.au.

Allison Steigler (A)

School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia.

David S Lamb (DS)

Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand.

Nigel A Spry (NA)

GenesisCare, Joondalup, Western Australia, Australia.

John Stanley (J)

Hollywood Specialist Centre, Nedlands, Western Australia, Australia.

Tom Shannon (T)

The Prostate Clinic, Nedlands, Western Australia, Australia.

Gillian Duchesne (G)

Peter MacCallum Cancer Centre and University of Melbourne, Victoria, Australia.

Chris Atkinson (C)

St Georges Cancer Care Centre, Christchurch, New Zealand.

John H L Matthews (JHL)

Cancer and Blood Services, Auckland District Health Board, Auckland, New Zealand.

Sandra Turner (S)

Crown Princess Mary Cancer Centre, Westmead Hospital, Sydney, New South Wales, Australia.

Lizbeth Kenny (L)

Royal Brisbane and Women's Hospital, Brisbane, Australia; School of Medicine, University of Queensland, Queensland, Australia.

David Christie (D)

Genesiscare, Tugun, Queensland, Australia.

Keen-Hun Tai (KH)

Peter MacCallum Cancer Centre and University of Melbourne, Victoria, Australia.

Nirdosh Kumar Gogna (NK)

Mater Radiation Oncology Centre, Princess Alexandra Hospital, Brisbane, Queensland, Australia.

Rachel Kearvell (R)

GenesisCare, St Andrew's Hospital, Adelaide, South Australia, Australia.

Judy Murray (J)

Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand.

Martin A Ebert (MA)

5D Clinics, Claremont, Western Australia, Australia; Department of Physics, University of Western Australia, Crawley, Western Australia, Australia.

Annette Haworth (A)

School of Physics, University of Sydney, Sydney, New South Wales.

Brett Delahunt (B)

Wellington School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand.

Christopher Oldmeadow (C)

School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia; Hunter Medical Research Institute, Newcastle, New South Wales, Australia.

John Attia (J)

School of Medicine and Public Health, University of Newcastle, Newcastle, New South Wales, Australia; Hunter Medical Research Institute, Newcastle, New South Wales, Australia.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH