Mortality Among Men with Advanced Prostate Cancer Excluded from the ProtecT Trial

被引:41
|
作者
Johnston, Thomas J. [1 ]
Shaw, Greg L. [1 ,2 ]
Lamb, Alastair D. [1 ,2 ]
Parashar, Deepak [3 ,4 ]
Greenberg, David [5 ]
Xiong, Tengbin [1 ]
Edwards, Alison L. [1 ]
Gnanapragasam, Vincent [1 ]
Holding, Peter [6 ]
Herbert, Phillipa [1 ]
Davis, Michael [7 ]
Mizielinsk, Elizabeth [7 ]
Lane, J. Athene [7 ]
Oxley, Jon [8 ]
Robinson, Mary [9 ]
Mason, Malcolm [10 ]
Staffurth, John [10 ]
Bollina, Prasad [11 ]
Catto, James [12 ]
Doble, Andrew [13 ]
Doherty, Alan [14 ]
Gillatt, David [15 ,16 ]
Kockelbergh, Roger [17 ]
Kynaston, Howard [18 ]
Prescott, Steve [19 ]
Paul, Alan [19 ]
Powell, Philip [20 ]
Rosario, Derek [12 ]
Rowe, Edward [15 ,16 ]
Donovan, Jenny L. [7 ]
Hamdy, Freddie C. [6 ]
Neal, David E. [1 ,6 ]
机构
[1] Univ Cambridge, Acad Urol Grp, Cambridge Biomed Campus, Cambridge CB2 0QQ, England
[2] Canc Res UK Cambridge Inst, Li Ka Shing Ctr, Cambridge, England
[3] Univ Warwick, Stat & Epidemiol Unit, Coventry, W Midlands, England
[4] Univ Warwick, Canc Res Ctr, Coventry, W Midlands, England
[5] Publ Hlth England, Eastern Off, Natl Canc Registrat Serv, Cambridge, England
[6] Univ Oxford, Nuffield Dept Surg Sci, Oxford, England
[7] Univ Bristol, Sch Social & Community Med, Bristol, Avon, England
[8] North Bristol NHS Trust, Dept Cellular Pathol, Bristol, Avon, England
[9] Royal Victoria Infirm, Dept Cellular Pathol, Newcastle Upon Tyne, Tyne & Wear, England
[10] Cardiff Univ, Sch Med, Div Canc & Genet, Cardiff, S Glam, Wales
[11] Univ Edinburgh, Western Gen Hosp, Dept Urol & Surg, Edinburgh, Midlothian, Scotland
[12] Univ Sheffield, Acad Urol Unit, Sheffield, S Yorkshire, England
[13] Addenbrookes Hosp, Dept Urol, Cambridge, England
[14] Queen Elizabeth Hosp, Dept Urol, Birmingham, W Midlands, England
[15] Southmead Hosp, Dept Urol, Bristol, Avon, England
[16] Bristol Urol Inst, Bristol, Avon, England
[17] Univ Hosp Leicester, Dept Urol, Leicester, Leics, England
[18] Cardiff & Vale Univ Hlth Board, Dept Urol, Cardiff, S Glam, Wales
[19] Leeds Teaching Hosp NHS Trust, Dept Urol, Leeds, W Yorkshire, England
[20] Freeman Rd Hosp, Dept Urol, Newcastle Upon Tyne, Tyne & Wear, England
关键词
Prostate cancer; Prostate-specific antigen screening; Survival; ANDROGEN-DEPRIVATION THERAPY; RADICAL PROSTATECTOMY; GENERAL-PRACTICE; TESTING RATES; PHASE-3; TRIAL; FOLLOW-UP; UK; RADIOTHERAPY; ENGLAND;
D O I
10.1016/j.eururo.2016.09.040
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
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 17 mu g/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. (C) 2016 European Association of Urology. Published by Elsevier B.V.
引用
收藏
页码:381 / 388
页数:8
相关论文
共 50 条
  • [21] A randomised controlled trial of a mindfulness intervention for men with advanced prostate cancer
    Chambers, Suzanne K.
    Smith, David P.
    Berry, Martin
    Lepore, Stephen J.
    Foley, Elizabeth
    Clutton, Samantha
    McDowall, Robert
    Occhipinti, Stefano
    Frydenberg, Mark
    Gardiner, Robert A.
    BMC CANCER, 2013, 13
  • [22] A randomised controlled trial of a mindfulness intervention for men with advanced prostate cancer
    Suzanne K Chambers
    David P Smith
    Martin Berry
    Stephen J Lepore
    Elizabeth Foley
    Samantha Clutton
    Robert McDowall
    Stefano Occhipinti
    Mark Frydenberg
    Robert A Gardiner
    BMC Cancer, 13
  • [23] Prostate cancer incidence and mortality rates among white and black men
    Merrill, RM
    Brawley, OW
    EPIDEMIOLOGY, 1997, 8 (02) : 126 - 131
  • [24] A prospective cohort and extended comprehensive-cohort design provided insights about the generalizability of a pragmatic trial: the ProtecT prostate cancer trial
    Donovan, Jenny L.
    Young, Grace J.
    Walsh, Eleanor I.
    Metcalfe, Chris
    Lane, J. Athene
    Martin, Richard M.
    Tazewell, Marta K.
    Davis, Michael
    Peters, Tim J.
    Turner, Emma L.
    Mills, Nicola
    Khazragui, Hanan
    Khera, Tarnjit K.
    Neal, David E.
    Hamdy, Freddie C.
    JOURNAL OF CLINICAL EPIDEMIOLOGY, 2018, 96 : 35 - 46
  • [25] Androgen deprivation therapy in the treatment of locally advanced, nonmetastatic prostate cancer: practical experience and a review of the clinical trial evidence
    Aoun, Fouad
    Bourgi, Ali
    Ayoub, Elias
    El Rassy, Elie
    van Velthoven, Roland
    Peltier, Alexandre
    THERAPEUTIC ADVANCES IN UROLOGY, 2017, 9 (3-4) : 73 - 80
  • [26] Comorbidity and Mortality Results From a Randomized Prostate Cancer Screening Trial
    Crawford, E. David
    Grubb, Robert, III
    Black, Amanda
    Andriole, Gerald L., Jr.
    Chen, Ming-Hui
    Izmirlian, Grant
    Berg, Christine D.
    D'Amico, Anthony V.
    JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (04) : 355 - 361
  • [27] Weight change, obesity and risk of prostate cancer progression among men with clinically localized prostate cancer
    Dickerman, Barbra A.
    Ahearn, Thomas U.
    Giovannucci, Edward
    Stampfer, Meir J.
    Nguyen, Paul L.
    Mucci, Lorelei A.
    Wilson, Kathryn M.
    INTERNATIONAL JOURNAL OF CANCER, 2017, 141 (05) : 933 - 944
  • [28] Is leisure time sitting associated with mortality rates among men diagnosed with localized prostate cancer?
    Bonn, Stephanie E.
    Holmberg, Erik
    Hugosson, Jonas
    Balter, Katarina
    EUROPEAN JOURNAL OF CANCER PREVENTION, 2020, 29 (02) : 134 - 140
  • [29] Prostate Cancer-Specific Mortality and the Extent of Therapy in Healthy Elderly Men With High-Risk Prostate Cancer
    Hoffman, Karen E.
    Chen, Ming-Hui
    Moran, Brian J.
    Braccioforte, Michelle H.
    Dosoretz, Daniel
    Salenius, Sharon
    Katin, Michael J.
    Ross, Rudi
    D'Amico, Anthony V.
    CANCER, 2010, 116 (11) : 2590 - 2595
  • [30] Use of Advanced Treatment Technologies Among Men at Low Risk of Dying From Prostate Cancer
    Jacobs, Bruce L.
    Zhang, Yun
    Schroeck, Florian R.
    Skolarus, Ted A.
    Wei, John T.
    Montie, James E.
    Gilbert, Scott M.
    Strope, Seth A.
    Dunn, Rodney L.
    Miller, David C.
    Hollenbeck, Brent K.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2013, 309 (24): : 2587 - 2595