TY - JOUR
T1 - Mortality Among Men with Advanced Prostate Cancer Excluded from the ProtecT Trial
AU - for the ProtecT Study Group
AU - Johnston, Thomas J.
AU - Shaw, Greg L.
AU - Lamb, Alastair D.
AU - Parashar, Deepak
AU - Greenberg, David
AU - Xiong, Tengbin
AU - Edwards, Alison L.
AU - Gnanapragasam, Vincent
AU - Holding, Peter
AU - Herbert, Phillipa
AU - Davis, Michael
AU - Mizielinsk, Elizabeth
AU - Lane, J. Athene
AU - Oxley, Jon
AU - Robinson, Mary
AU - Mason, Malcolm
AU - Staffurth, John
AU - Bollina, Prasad
AU - Catto, James
AU - Doble, Andrew
AU - Doherty, Alan
AU - Gillatt, David
AU - Kockelbergh, Roger
AU - Kynaston, Howard
AU - Prescott, Steve
AU - Paul, Alan
AU - Powell, Philip
AU - Rosario, Derek
AU - Rowe, Edward
AU - Donovan, Jenny L.
AU - Hamdy, Freddie C.
AU - Neal, David E.
N1 - Publisher Copyright:
© 2016 European Association of Urology
PY - 2017/3/1
Y1 - 2017/3/1
N2 - 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 μg/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.
AB - 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 μg/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.
KW - Prostate cancer
KW - Prostate-specific antigen screening
KW - Survival
UR - http://www.scopus.com/inward/record.url?scp=84991824441&partnerID=8YFLogxK
U2 - 10.1016/j.eururo.2016.09.040
DO - 10.1016/j.eururo.2016.09.040
M3 - Article
C2 - 27720537
AN - SCOPUS:84991824441
SN - 0302-2838
VL - 71
SP - 381
EP - 388
JO - European Urology
JF - European Urology
IS - 3
ER -