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Mortality Among Men with Advanced Prostate Cancer Excluded from the ProtecT Trial.
Johnston, Thomas J; Shaw, Greg L; Lamb, Alastair D; Parashar, Deepak; Greenberg, David; Xiong, Tengbin; Edwards, Alison L; Gnanapragasam, Vincent; Holding, Peter; Herbert, Phillipa; Davis, Michael; Mizielinsk, Elizabeth; Lane, J Athene; Oxley, Jon; Robinson, Mary; Mason, Malcolm; Staffurth, John; Bollina, Prasad; Catto, James; Doble, Andrew; Doherty, Alan; Gillatt, David; Kockelbergh, Roger; Kynaston, Howard; Prescott, Steve; Paul, Alan; Powell, Philip; Rosario, Derek; Rowe, Edward; Donovan, Jenny L; Hamdy, Freddie C; Neal, David E.
Affiliation
  • Johnston TJ; Academic Urology Group, University of Cambridge, Cambridge, UK. Electronic address: thomasjohnston1@nhs.net.
  • Shaw GL; Academic Urology Group, University of Cambridge, Cambridge, UK; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK.
  • Lamb AD; Academic Urology Group, University of Cambridge, Cambridge, UK; Cancer Research UK Cambridge Institute, Li Ka Shing Centre, Cambridge, UK.
  • Parashar D; Statistics and Epidemiology Unit & Cancer Research Centre, University of Warwick, Coventry, UK.
  • Greenberg D; National Cancer Registration Service - Eastern Office, Public Health England, Cambridge, UK.
  • Xiong T; Academic Urology Group, University of Cambridge, Cambridge, UK.
  • Edwards AL; Academic Urology Group, University of Cambridge, Cambridge, UK.
  • Gnanapragasam V; Academic Urology Group, University of Cambridge, Cambridge, UK.
  • Holding P; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
  • Herbert P; Academic Urology Group, University of Cambridge, Cambridge, UK.
  • Davis M; School of Social and Community Medicine, University of Bristol, Bristol, UK.
  • Mizielinsk E; School of Social and Community Medicine, University of Bristol, Bristol, UK.
  • Lane JA; School of Social and Community Medicine, University of Bristol, Bristol, UK.
  • Oxley J; Department of Cellular Pathology, North Bristol NHS Trust, Bristol, UK.
  • Robinson M; Department of Cellular Pathology, Royal Victoria Infirmary, Newcastle-upon-Tyne, UK.
  • Mason M; Division of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
  • Staffurth J; Division of Cancer and Genetics, School of Medicine, Cardiff University, Cardiff, UK.
  • Bollina P; Department of Urology and Surgery, Western General Hospital, University of Edinburgh, Edinburgh, UK.
  • Catto J; Academic Urology Unit, University of Sheffield, Sheffield, UK.
  • Doble A; Department of Urology, Addenbrooke's Hospital, Cambridge, UK.
  • Doherty A; Department of Urology, Queen Elizabeth Hospital, Birmingham, UK.
  • Gillatt D; Department of Urology, Southmead Hospital and Bristol Urological Institute, Bristol, UK.
  • Kockelbergh R; Department of Urology, University Hospitals of Leicester, Leicester, UK.
  • Kynaston H; Department of Urology, Cardiff and Vale University Health Board, Cardiff, UK.
  • Prescott S; Department of Urology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Paul A; Department of Urology, Leeds Teaching Hospitals NHS Trust, Leeds, UK.
  • Powell P; Department of Urology, Freeman Hospital, Newcastle-upon-Tyne, UK.
  • Rosario D; Academic Urology Unit, University of Sheffield, Sheffield, UK.
  • Rowe E; Department of Urology, Southmead Hospital and Bristol Urological Institute, Bristol, UK.
  • Donovan JL; School of Social and Community Medicine, University of Bristol, Bristol, UK.
  • Hamdy FC; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
  • Neal DE; Academic Urology Group, University of Cambridge, Cambridge, UK; Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK. Electronic address: den22@cam.ac.uk.
Eur Urol ; 71(3): 381-388, 2017 03.
Article in En | MEDLINE | ID: mdl-27720537
ABSTRACT

BACKGROUND:

Early detection and treatment of asymptomatic men with advanced and high-risk prostate cancer (PCa) may improve survival rates.

OBJECTIVE:

To determine outcomes for men diagnosed with advanced PCa following prostate-specific antigen (PSA) testing who were excluded from the ProtecT randomised trial. DESIGN, SETTING, AND

PARTICIPANTS:

Mortality was compared for 492 men followed up for a median of 7.4 yr to a contemporaneous cohort of men from the UK Anglia Cancer Network (ACN) and with a matched subset from the ACN. OUTCOME MEASUREMENTS AND STATISTICAL

ANALYSIS:

PCa-specific and all-cause mortality were compared using Kaplan-Meier analysis and Cox's proportional hazards regression. RESULTS AND

LIMITATIONS:

Of the 492 men excluded from the ProtecT cohort, 37 (8%) had metastases (N1, M0=5, M1=32) and 305 had locally advanced disease (62%). The median PSA was 17µg/l. Treatments included radical prostatectomy (RP; n=54; 11%), radiotherapy (RT; n=245; 50%), androgen deprivation therapy (ADT; n=122; 25%), other treatments (n=11; 2%), and unknown (n=60; 12%). There were 49 PCa-specific deaths (10%), of whom 14 men had received radical treatment (5%); and 129 all-cause deaths (26%). In matched ProtecT and ACN cohorts, 37 (9%) and 64 (16%), respectively, died of PCa, while 89 (22%) and 103 (26%) died of all causes. ProtecT men had a 45% lower risk of death from PCa compared to matched cases (hazard ratio 0.55, 95% confidence interval 0.38-0.83; p=0.0037), but mortality was similar in those treated radically. The nonrandomised design is a limitation.

CONCLUSIONS:

Men with PSA-detected advanced PCa excluded from ProtecT and treated radically had low rates of PCa death at 7.4-yr follow-up. Among men who underwent nonradical treatment, the ProtecT group had a lower rate of PCa death. Early detection through PSA testing, leadtime bias, and group heterogeneity are possible factors in this finding. PATIENT

SUMMARY:

Prostate cancer that has spread outside the prostate gland without causing symptoms can be detected via prostate-specific antigen testing and treated, leading to low rates of death from this disease.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Mortality Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Aged / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Eur Urol Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Mortality Type of study: Clinical_trials / Diagnostic_studies / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limits: Aged / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Eur Urol Year: 2017 Document type: Article