Radiotherapy to the prostate for men with metastatic prostate cancer in the UK and Switzerland: Long-term results from the STAMPEDE randomised controlled trial.


Journal

PLoS medicine
ISSN: 1549-1676
Titre abrégé: PLoS Med
Pays: United States
ID NLM: 101231360

Informations de publication

Date de publication:
06 2022
Historique:
received: 04 01 2022
accepted: 22 04 2022
entrez: 7 6 2022
pubmed: 8 6 2022
medline: 10 6 2022
Statut: epublish

Résumé

STAMPEDE has previously reported that radiotherapy (RT) to the prostate improved overall survival (OS) for patients with newly diagnosed prostate cancer with low metastatic burden, but not those with high-burden disease. In this final analysis, we report long-term findings on the primary outcome measure of OS and on the secondary outcome measures of symptomatic local events, RT toxicity events, and quality of life (QoL). Patients were randomised at secondary care sites in the United Kingdom and Switzerland between January 2013 and September 2016, with 1:1 stratified allocation: 1,029 to standard of care (SOC) and 1,032 to SOC+RT. No masking of the treatment allocation was employed. A total of 1,939 had metastatic burden classifiable, with 42% low burden and 58% high burden, balanced by treatment allocation. Intention-to-treat (ITT) analyses used Cox regression and flexible parametric models (FPMs), adjusted for stratification factors age, nodal involvement, the World Health Organization (WHO) performance status, regular aspirin or nonsteroidal anti-inflammatory drug (NSAID) use, and planned docetaxel use. QoL in the first 2 years on trial was assessed using prospectively collected patient responses to QLQ-30 questionnaire. Patients were followed for a median of 61.3 months. Prostate RT improved OS in patients with low, but not high, metastatic burden (respectively: 202 deaths in SOC versus 156 in SOC+RT, hazard ratio (HR) = 0·64, 95% CI 0.52, 0.79, p < 0.001; 375 SOC versus 386 SOC+RT, HR = 1.11, 95% CI 0.96, 1.28, p = 0·164; interaction p < 0.001). No evidence of difference in time to symptomatic local events was found. There was no evidence of difference in Global QoL or QLQ-30 Summary Score. Long-term urinary toxicity of grade 3 or worse was reported for 10 SOC and 10 SOC+RT; long-term bowel toxicity of grade 3 or worse was reported for 15 and 11, respectively. Prostate RT improves OS, without detriment in QoL, in men with low-burden, newly diagnosed, metastatic prostate cancer, indicating that it should be recommended as a SOC. ClinicalTrials.gov NCT00268476, ISRCTN.com ISRCTN78818544.

Sections du résumé

BACKGROUND
STAMPEDE has previously reported that radiotherapy (RT) to the prostate improved overall survival (OS) for patients with newly diagnosed prostate cancer with low metastatic burden, but not those with high-burden disease. In this final analysis, we report long-term findings on the primary outcome measure of OS and on the secondary outcome measures of symptomatic local events, RT toxicity events, and quality of life (QoL).
METHODS AND FINDINGS
Patients were randomised at secondary care sites in the United Kingdom and Switzerland between January 2013 and September 2016, with 1:1 stratified allocation: 1,029 to standard of care (SOC) and 1,032 to SOC+RT. No masking of the treatment allocation was employed. A total of 1,939 had metastatic burden classifiable, with 42% low burden and 58% high burden, balanced by treatment allocation. Intention-to-treat (ITT) analyses used Cox regression and flexible parametric models (FPMs), adjusted for stratification factors age, nodal involvement, the World Health Organization (WHO) performance status, regular aspirin or nonsteroidal anti-inflammatory drug (NSAID) use, and planned docetaxel use. QoL in the first 2 years on trial was assessed using prospectively collected patient responses to QLQ-30 questionnaire. Patients were followed for a median of 61.3 months. Prostate RT improved OS in patients with low, but not high, metastatic burden (respectively: 202 deaths in SOC versus 156 in SOC+RT, hazard ratio (HR) = 0·64, 95% CI 0.52, 0.79, p < 0.001; 375 SOC versus 386 SOC+RT, HR = 1.11, 95% CI 0.96, 1.28, p = 0·164; interaction p < 0.001). No evidence of difference in time to symptomatic local events was found. There was no evidence of difference in Global QoL or QLQ-30 Summary Score. Long-term urinary toxicity of grade 3 or worse was reported for 10 SOC and 10 SOC+RT; long-term bowel toxicity of grade 3 or worse was reported for 15 and 11, respectively.
CONCLUSIONS
Prostate RT improves OS, without detriment in QoL, in men with low-burden, newly diagnosed, metastatic prostate cancer, indicating that it should be recommended as a SOC.
TRIAL REGISTRATION
ClinicalTrials.gov NCT00268476, ISRCTN.com ISRCTN78818544.

Identifiants

pubmed: 35671327
doi: 10.1371/journal.pmed.1003998
pii: PMEDICINE-D-22-00022
pmc: PMC9173627
doi:

Substances chimiques

Docetaxel 15H5577CQD

Banques de données

ClinicalTrials.gov
['NCT00268476']
ISRCTN
['ISRCTN78818544']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e1003998

Subventions

Organisme : Medical Research Council
ID : MC_UU_00004/02
Pays : United Kingdom
Organisme : Cancer Research UK
ID : CRUK_A12459
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_00004/01
Pays : United Kingdom
Organisme : Medical Research Council
ID : MRC_MC_UU_12023/25
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_UU_12023/25
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 12518
Pays : United Kingdom
Organisme : Cancer Research UK
ID : 3804
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: CCP reports personal fees from Bayer, personal fees from Janssen, personal fees from Clarity Pharmaceuticals, personal fees from Myovant, personal fees from ITM Oncologics, outside the submitted work NDJ received research funding to the institution from Astellas, Astra Zeneca &Janssen; receipt of honoraria/fees on the advisory board for Astra Zenenca, Clovis, Janssen, Merck, Novartis & Sanofi; received fees as a speaker for Bayer & Novartis NWC received honoraria from Astellas & Janssen; took a consulting/advisory role for Astellas, Janssen, Ferring, Bayer & Sanofi; was paid speakers fees b Janssen & Astellas; received funding for the institution from Astra Zeneca; received meeting and travel expenses from Janssen, Astellas, Sanofi, Astra Zeneca, Ferring & Ipsen GA reports personal fees from Sanofi Aventis, during the conduct of the study; personal fees and non-financial support from Astellas, personal fees and non-financial support from Medivation, personal fees from Novartis, personal fees from Millennium Pharmaceuticals, personal fees and non-financial support from Abbott Laboratories, personal fees and non-financial support from Essa Pharmaceuticals, personal fees and non-financial support from Bayer Healthcare Pharmaceuticals, personal fees from Takeda, grants from AstraZeneca, grants from Arno Therapeutics, grants from Innocrin Pharma, grants, personal fees and non-financial support from Janssen, personal fees from Veridex, personal fees and non-financial support from Roche/Ventana, personal fees and non-financial support from Pfizer, personal fees from The Institute of Cancer Research (ICR), outside the submitted work; and The Institute of Cancer Research (ICR) receives royalty income from abiraterone I receive a share of this income through the ICR’s Rewards to Discoverers Scheme SC received consulting fees from Telix, remedy & Huma; received payment for speaker fees and/or manuscript writing and/or educational events from Astra Zeneca, Novartis/AAA, Clovis, Janssen, Bayer, Pfizer, Beigene & Astellas; they were a member of the data safety monitoring/advisory board for Astra Zeneca, Novartis/AAA, Clovis, Janssen, Bayer, Pfizer, Beigene & Astellas DPD received payment to the institution from C33589/A19727 Advances in Physics for Precision Radiotherapy; previous employer, The Institute of Cancer Research receives loyalty income from abiraterone, receives personal share of this income through ICR’s Rewards to Discoverer’s Scheme; honoraria for consultancy from Janssen; EP1933709B1 – Location and Stabilisation Device., European patent issued, Pending in Canada and India SG reports personal fees from Orion, personal fees from Janssen Cilag, personal fees from ProteoMedix, personal fees from Amgen, personal fees from MSD, other from Tolero Pharmaceuticals, other from Astellas Pharma, other from Janssen, other from MSD Merck Sharp&Dome, other from Bayer, other from Roche, other from Pfizer, other from Telixpharma, other from Amgen, other from Bristol-Myers Squibb, other from AAA International SA, other from Orion, other from Silvio Grasso Consulting, from Tolremo, outside the submitted work; In addition, Gillessen has a patent WO2009138392 issued and Menarini Silicon Biosystems (Advisory Board 2019) - not compensated Aranda (Advisory Board 2019) - not compensated RJJ received research funding to the institution from Bayer, Astellas & Pfizer; received honoraria on the advisory board for Janssen, Astellas, Bayer, Pfizer; received speaker fees from Janssen, Astellas, Bayer & Pfizer REL received an institutional grant from the MRC CG received research funding to the institution from Janssen, Clovis Oncology, Sanofi, Astellas, Medical Research Council & Cancer Research UK DF received speaker fees and/or manuscript writing and/or educational events from BMS, IPSEN, EUSA, Pfizer, ESAI; they received travel expenses from Janssen & IPSEN MDM is an advisory board member for Endocyte & Clovis AB received payment for lecture/presentation/speaker bureau/manuscript writing or educational event from Boston Scientific AJB received speaker fees and travel support from Janssen DF received payment for lectures for Janssen, Pfizer & BMS; support for attending conferences/meetings from Genisiscare & BMS AMH received research grants from CRUK and NIHR; support attending meetings from the European Association of Urologists; is a member of the European Association of Urologists & the Prostate Cancer Guidelines Group MK received travel, accommodation and conference fees as expenses from Bayer, travel and accommodation fees for Prostate cancer summits from Janssen AL received expenses for attending meetings and/or travel from Astellas, Bayer, BMS & MSD JMOS received speaker fees from AAA, Astellas, Bayer, Janssen, Novartis, Sanofi and participated as an advisory board member and/or member of the data safety monitoring board for AAA, Astellas, Bayer, Janssen, Novartis & Sanofi NNS received travel/meeting payments from Janssen JT received support for conference attendance from Janssen, Roche & Bayer; participated on the advisory board for Astra Zeneca, Astellas & Bayer MKBP received research funding to the Unit he directs from Acoria Pvt Ltd, Akagera, Amgen, Aspirin Foundation, Astellas, AstraZeneca, Baxter, Bayer, BMS US, Bri-Bio, Cepheid, Cipla, Clovis Inc, CSL Behring, Eli-Lilly, Emergent Biosolutions, Gilead Sciences, GlaxoSmithKline, Grifols, Janssen Products LP, Janssen-Cilag, Johnson & Johnson, Micronoma, Modus Theraputics, Mylan, Novartis, Pfizer, Sanofi, Serum Institute of India, Shionogi, Synteny Biotechnology, Takeda, Tibotec, Transgene, ViiV Healthcare, Virco and Xenothera MRS received research funding to the institution from Astellas, Clovis, Janssen, Novartis, Pfizer, Sanofi-Aventis; received speaker fees from Lilly Oncology & Janssen; independent member of data monitoring committees. All other authors have nothing to declare.

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Auteurs

Chris C Parker (CC)

The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, United Kingdom.

Nicholas D James (ND)

The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, United Kingdom.

Christopher D Brawley (CD)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Noel W Clarke (NW)

The Christie Hospital, Manchester, United Kingdom.
Salford Royal Hospitals, Manchester, United Kingdom.

Adnan Ali (A)

The Christie Hospital, Manchester, United Kingdom.

Claire L Amos (CL)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Gerhardt Attard (G)

UCL Cancer Institute, UCL, London, United Kingdom.

Simon Chowdhury (S)

Guys and St Thomas's NHS Foundation Trust, London, United Kingdom.

Adrian Cook (A)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

William Cross (W)

St James's University Hospital, Leeds, United Kingdom.

David P Dearnaley (DP)

The Institute of Cancer Research and Royal Marsden NHS Foundation Trust, London, United Kingdom.

Hassan Douis (H)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Duncan C Gilbert (DC)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Clare Gilson (C)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Silke Gillessen (S)

Istituto Oncologico della Svizzera Italiana, EOC, Bellinzona, Switzerland.
Università della Svizzera Italiana, Lugano, Switzerland.

Alex Hoyle (A)

The Christie Hospital, Manchester, United Kingdom.
Salford Royal Hospitals, Manchester, United Kingdom.

Rob J Jones (RJ)

Institute of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Ruth E Langley (RE)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Zafar I Malik (ZI)

Clatterbridge Cancer Centre, Liverpool, United Kingdom.

Malcolm D Mason (MD)

Cardiff University, Cardiff, United Kingdom.

David Matheson (D)

University of Wolverhampton, Wolverhampton, United Kingdom.

Robin Millman (R)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Mary Rauchenberger (M)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Hannah Rush (H)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.
Guys and St Thomas's NHS Foundation Trust, London, United Kingdom.

J Martin Russell (JM)

Institute of Cancer Sciences, University of Glasgow, Glasgow, United Kingdom.

Hannah Sweeney (H)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Amit Bahl (A)

University Hospitals Bristol NHS Trust, Bristol, United Kingdom.

Alison Birtle (A)

Rosemere Cancer Centre, Lancs Teaching Hospitals, University of Manchester, Manchester, United Kingdom.
UCLan, Lanchashire, United Kingdom.

Lisa Capaldi (L)

Worcestershire Acute Hospitals NHS Trust, Worcester, United Kingdom.

Omar Din (O)

Weston Park Cancer Centre, Sheffield, United Kingdom.

Daniel Ford (D)

University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom.

Joanna Gale (J)

Queen Alexandra Hospital, Portsmouth, United Kingdom.

Ann Henry (A)

University of Leeds, Leeds, United Kingdom.

Peter Hoskin (P)

The Christie Hospital, Manchester, United Kingdom.
Mount Vernon Cancer Centre, Northwood, United Kingdom.

Mohammed Kagzi (M)

The James Cook University Hospital, Middlesbrough, United Kingdom.

Anna Lydon (A)

Torbay and South Devon NHS Trust, Torbay, United Kingdom.

Joe M O'Sullivan (JM)

Patrick G Johnston Centre for Cancer Research, Queen's University Belfast, United Kingdom.

Sangeeta A Paisey (SA)

Hampshire Hospitals NHS Foundation Trust, Hampshire, United Kingdom.

Omi Parikh (O)

Royal Preston Hospital, Preston, United Kingdom.

Delia Pudney (D)

South West Wales Cancer Centre, Swansea, United Kingdom.

Vijay Ramani (V)

The Christie Hospital, Manchester, United Kingdom.
Manchester University Hospitals NHS Trust, Manchester, United Kingdom.

Peter Robson (P)

Clatterbridge Cancer Centre, Liverpool, United Kingdom.

Narayanan Nair Srihari (NN)

Shrewsbury & Telford Hospitals NHS Trust, Shrewsbury, United Kingdom.

Jacob Tanguay (J)

Velindre Cancer Centre, Cardiff, United Kingdom.

Mahesh K B Parmar (MKB)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

Matthew R Sydes (MR)

MRC Clinical Trials Unit at UCL, UCL, London, United Kingdom.

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