Summary statement on screening for prostate cancer in Europe
The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate‐Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can out...
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Published in | International journal of cancer Vol. 142; no. 4; pp. 741 - 746 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Wiley Subscription Services, Inc
15.02.2018
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Online Access | Get full text |
ISSN | 0020-7136 1097-0215 1097-0215 |
DOI | 10.1002/ijc.31102 |
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Abstract | The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate‐Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can outweigh the harms if screening is stopped in older ages to prevent overdiagnosis. A limited screening program (for example screening at ages 55–59 years), including active surveillance for men with low‐risk tumors, can even be cost‐saving, compared with testing in an opportunistic setting in the wrong ages, as currently in Europe. Further improvements are expected in the use of active surveillance and in discrimination between indolent and significant disease due to new biomarkers and magnetic resonance imaging. However, these future developments are no reason to postpone feasibility studies of high‐quality PSA screening and reduce opportunistic testing at old ages.
What's new?
This article is a summary of the European consensus meeting where more than 30 experts discussed the benefits, harms, and cost‐effectiveness of prostate cancer screening. The participants strongly agreed that Prostate‐Specific Antigen (PSA) screening can substantially reduce prostate cancer mortality. Concerns over overdiagnosis and overtreatment remained, however. The experts found that the benefits can outweigh the harms if screening is stopped in older ages. A limited screening program (in screens and age range), including active surveillance for men with low‐risk tumors, can even be cost‐saving. The experts recommend starting pilot studies for the implementation of limited, organised prostate cancer screening. |
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AbstractList | The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate-Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can outweigh the harms if screening is stopped in older ages to prevent overdiagnosis. A limited screening program (for example screening at ages 55-59 years), including active surveillance for men with low-risk tumors, can even be cost-saving, compared with testing in an opportunistic setting in the wrong ages, as currently in Europe. Further improvements are expected in the use of active surveillance and in discrimination between indolent and significant disease due to new biomarkers and magnetic resonance imaging. However, these future developments are no reason to postpone feasibility studies of high-quality PSA screening and reduce opportunistic testing at old ages. What's new? This article is a summary of the European consensus meeting where more than 30 experts discussed the benefits, harms, and cost-effectiveness of prostate cancer screening. The participants strongly agreed that Prostate-Specific Antigen (PSA) screening can substantially reduce prostate cancer mortality. Concerns over overdiagnosis and overtreatment remained, however. The experts found that the benefits can outweigh the harms if screening is stopped in older ages. A limited screening program (in screens and age range), including active surveillance for men with low-risk tumors, can even be cost-saving. The experts recommend starting pilot studies for the implementation of limited, organised prostate cancer screening. The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate‐Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can outweigh the harms if screening is stopped in older ages to prevent overdiagnosis. A limited screening program (for example screening at ages 55–59 years), including active surveillance for men with low‐risk tumors, can even be cost‐saving, compared with testing in an opportunistic setting in the wrong ages, as currently in Europe. Further improvements are expected in the use of active surveillance and in discrimination between indolent and significant disease due to new biomarkers and magnetic resonance imaging. However, these future developments are no reason to postpone feasibility studies of high‐quality PSA screening and reduce opportunistic testing at old ages. What's new? This article is a summary of the European consensus meeting where more than 30 experts discussed the benefits, harms, and cost‐effectiveness of prostate cancer screening. The participants strongly agreed that Prostate‐Specific Antigen (PSA) screening can substantially reduce prostate cancer mortality. Concerns over overdiagnosis and overtreatment remained, however. The experts found that the benefits can outweigh the harms if screening is stopped in older ages. A limited screening program (in screens and age range), including active surveillance for men with low‐risk tumors, can even be cost‐saving. The experts recommend starting pilot studies for the implementation of limited, organised prostate cancer screening. The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate-Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can outweigh the harms if screening is stopped in older ages to prevent overdiagnosis. A limited screening program (for example screening at ages 55-59 years), including active surveillance for men with low-risk tumors, can even be cost-saving, compared with testing in an opportunistic setting in the wrong ages, as currently in Europe. Further improvements are expected in the use of active surveillance and in discrimination between indolent and significant disease due to new biomarkers and magnetic resonance imaging. However, these future developments are no reason to postpone feasibility studies of high-quality PSA screening and reduce opportunistic testing at old ages. The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate-Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can outweigh the harms if screening is stopped in older ages to prevent overdiagnosis. A limited screening program (for example screening at ages 55-59 years), including active surveillance for men with low-risk tumors, can even be cost-saving, compared with testing in an opportunistic setting in the wrong ages, as currently in Europe. Further improvements are expected in the use of active surveillance and in discrimination between indolent and significant disease due to new biomarkers and magnetic resonance imaging. However, these future developments are no reason to postpone feasibility studies of high-quality PSA screening and reduce opportunistic testing at old ages.The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate-Specific Antigen (PSA) based screening results in a significant prostate cancer mortality reduction. Although there are concerns on overdiagnosis and overtreatment, it has been shown that the benefits can outweigh the harms if screening is stopped in older ages to prevent overdiagnosis. A limited screening program (for example screening at ages 55-59 years), including active surveillance for men with low-risk tumors, can even be cost-saving, compared with testing in an opportunistic setting in the wrong ages, as currently in Europe. Further improvements are expected in the use of active surveillance and in discrimination between indolent and significant disease due to new biomarkers and magnetic resonance imaging. However, these future developments are no reason to postpone feasibility studies of high-quality PSA screening and reduce opportunistic testing at old ages. |
Author | Borràs, Josep M. de Carvalho, Tiago M. Castells, Xavier Vandenbulcke, Pieter Lansdorp‐Vogelaar, Iris Heijnsdijk, Eveline A.M. Eklund, Martin de Koning, Harry J. Recker, Franz Roobol, Monique J. Espinàs, Josep A. Leeuwen, Pim J. van Graefen, Markus Grönberg, Henrik Bangma, Chris H. Nelen, Vera |
Author_xml | – sequence: 1 givenname: Eveline A.M. orcidid: 0000-0002-4890-6069 surname: Heijnsdijk fullname: Heijnsdijk, Eveline A.M. email: e.heijnsdijk@erasmusmc.nl organization: Erasmus Medical Center, Wytemaweg 80 – sequence: 2 givenname: Chris H. surname: Bangma fullname: Bangma, Chris H. organization: Erasmus Medical Center, Wytemaweg 80 – sequence: 3 givenname: Josep M. surname: Borràs fullname: Borràs, Josep M. organization: Catalan Institute of Oncology, Avinguda de la Granvia de l'Hospitalet 199‐203 – sequence: 4 givenname: Tiago M. surname: de Carvalho fullname: de Carvalho, Tiago M. organization: Erasmus Medical Center, Wytemaweg 80 – sequence: 5 givenname: Xavier surname: Castells fullname: Castells, Xavier organization: IMIM (Hospital del Mar Medical Research Institute), Passeig Marítim, 25‐29 – sequence: 6 givenname: Martin surname: Eklund fullname: Eklund, Martin organization: Karolinska Institutet, Karolinska vägen – sequence: 7 givenname: Josep A. surname: Espinàs fullname: Espinàs, Josep A. organization: Catalan Institute of Oncology, Avinguda de la Granvia de l'Hospitalet 199‐203 – sequence: 8 givenname: Markus surname: Graefen fullname: Graefen, Markus organization: Martini‐Clinic, Prostate Cancer Center, University Medical Center Hamburg‐Eppendorf, Martinistrasse 52 Building O43 – sequence: 9 givenname: Henrik surname: Grönberg fullname: Grönberg, Henrik organization: Karolinska Institutet, Karolinska vägen – sequence: 10 givenname: Iris surname: Lansdorp‐Vogelaar fullname: Lansdorp‐Vogelaar, Iris organization: Erasmus Medical Center, Wytemaweg 80 – sequence: 11 givenname: Pim J. van surname: Leeuwen fullname: Leeuwen, Pim J. van organization: Erasmus Medical Center, Wytemaweg 80 – sequence: 12 givenname: Vera surname: Nelen fullname: Nelen, Vera organization: Provinciaal Instituut voor Hygiëne, Kronenburgstraat 45 – sequence: 13 givenname: Franz surname: Recker fullname: Recker, Franz organization: Kantonsspital Aarau, Tellstrasse 25 – sequence: 14 givenname: Monique J. surname: Roobol fullname: Roobol, Monique J. organization: Erasmus Medical Center, Wytemaweg 80 – sequence: 15 givenname: Pieter surname: Vandenbulcke fullname: Vandenbulcke, Pieter organization: Agentschap Zorg en gezondheid, Lange Kievitstraat 111‐113 – sequence: 16 givenname: Harry J. surname: de Koning fullname: de Koning, Harry J. organization: Erasmus Medical Center, Wytemaweg 80 |
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Snippet | The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate‐Specific Antigen (PSA) based screening results in a significant... The European Randomised Study of Screening for Prostate Cancer (ERSPC) showed that Prostate-Specific Antigen (PSA) based screening results in a significant... |
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SubjectTerms | Antigens Cancer Cancer screening Feasibility studies Magnetic resonance imaging mass‐screening Medical research Medical screening Mortality Prostate cancer Prostate-specific antigen PSA Surveillance Tumors |
Title | Summary statement on screening for prostate cancer in Europe |
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