Population-based screening for cancer: hope and hype
Key Points Tumours within any organ site can have a spectrum of biological phenotypes, ranging from indolent to highly aggressive Screening for cancer is most likely to be beneficial when the target tumour type has a relatively uniform biology and a slower rate of progression Not all precursor lesio...
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Published in | Nature reviews. Clinical oncology Vol. 13; no. 9; pp. 550 - 565 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.09.2016
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Abstract | Key Points
Tumours within any organ site can have a spectrum of biological phenotypes, ranging from indolent to highly aggressive
Screening for cancer is most likely to be beneficial when the target tumour type has a relatively uniform biology and a slower rate of progression
Not all precursor lesions are on an obligate pathway towards invasive-cancer development
Strategies for early detection of cancer must balance the benefits of mortality reduction (and reduction in invasive-disease incidence with screening for precancers) with the heterogeneity of the target disease and the consequent risk of overdiagnosis
Screening can be viewed as a 'cascade' involving multiple steps, such as selection of individuals to be screened, administration of the screening test, workup of positive findings, and, ultimately, treatment
Efforts are underway to individualize decision-making surrounding risk stratification, the modality and frequency of screening, and diagnostic and therapeutic interventions tailored to the biology of the detected tumour
Considerable hope, as well as a substantial degree of hype, has surrounded cancer-screening programmes, but current practices are suboptimal and are the subject of continued improvement efforts. In this Review, the authors discuss the experiences to date in screening for breast, cervical, colorectal, lung and prostate cancers, outline the lessons we have learned, and describe how this knowledge is informing improvements in cancer screening, with the hope they will eventually live up to the hype.
Several important lessons have been learnt from our experiences in screening for various cancers. Screening programmes for cervical and colorectal cancers have had the greatest success, probably because these cancers are relatively homogenous, slow-growing, and have identifiable precursors that can be detected and removed; however, identifying the true obligate precursors of invasive disease remains a challenge. With regard to screening for breast cancer and for prostate cancer, which focus on early detection of invasive cancer, preferential detection of slower-growing, localized cancers has occurred, which has led to concerns about overdiagnosis and overtreatment; programmes for early detection of invasive lung cancers are emerging, and have faced similar challenges. A crucial consideration in screening for breast, prostate, and lung cancers is their remarkable phenotypic heterogeneity, ranging from indolent to highly aggressive. Efforts have been made to address the limitations of cancer-screening programmes, providing an opportunity for cross-disciplinary learning and further advancement of the science. Current innovations are aimed at identifying the individuals who are most likely to benefit from screening, increasing the yield of consequential cancers on screening and biopsy, and using molecular tests to improve our understanding of disease biology and to tailor treatment. We discuss each of these concepts and outline a dynamic framework for continuous improvements in the field of cancer screening. |
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AbstractList | Several important lessons have been learnt from our experiences in screening for various cancers. Screening programmes for cervical and colorectal cancers have had the greatest success, probably because these cancers are relatively homogenous, slow-growing, and have identifiable precursors that can be detected and removed; however, identifying the true obligate precursors of invasive disease remains a challenge. With regard to screening for breast cancer and for prostate cancer, which focus on early detection of invasive cancer, preferential detection of slower-growing, localized cancers has occurred, which has led to concerns about overdiagnosis and overtreatment; programmes for early detection of invasive lung cancers are emerging, and have faced similar challenges. A crucial consideration in screening for breast, prostate, and lung cancers is their remarkable phenotypic heterogeneity, ranging from indolent to highly aggressive. Efforts have been made to address the limitations of cancer-screening programmes, providing an opportunity for cross-disciplinary learning and further advancement of the science. Current innovations are aimed at identifying the individuals who are most likely to benefit from screening, increasing the yield of consequential cancers on screening and biopsy, and using molecular tests to improve our understanding of disease biology and to tailor treatment. We discuss each of these concepts and outline a dynamic framework for continuous improvements in the field of cancer screening. Key Points Tumours within any organ site can have a spectrum of biological phenotypes, ranging from indolent to highly aggressive Screening for cancer is most likely to be beneficial when the target tumour type has a relatively uniform biology and a slower rate of progression Not all precursor lesions are on an obligate pathway towards invasive-cancer development Strategies for early detection of cancer must balance the benefits of mortality reduction (and reduction in invasive-disease incidence with screening for precancers) with the heterogeneity of the target disease and the consequent risk of overdiagnosis Screening can be viewed as a 'cascade' involving multiple steps, such as selection of individuals to be screened, administration of the screening test, workup of positive findings, and, ultimately, treatment Efforts are underway to individualize decision-making surrounding risk stratification, the modality and frequency of screening, and diagnostic and therapeutic interventions tailored to the biology of the detected tumour Considerable hope, as well as a substantial degree of hype, has surrounded cancer-screening programmes, but current practices are suboptimal and are the subject of continued improvement efforts. In this Review, the authors discuss the experiences to date in screening for breast, cervical, colorectal, lung and prostate cancers, outline the lessons we have learned, and describe how this knowledge is informing improvements in cancer screening, with the hope they will eventually live up to the hype. Several important lessons have been learnt from our experiences in screening for various cancers. Screening programmes for cervical and colorectal cancers have had the greatest success, probably because these cancers are relatively homogenous, slow-growing, and have identifiable precursors that can be detected and removed; however, identifying the true obligate precursors of invasive disease remains a challenge. With regard to screening for breast cancer and for prostate cancer, which focus on early detection of invasive cancer, preferential detection of slower-growing, localized cancers has occurred, which has led to concerns about overdiagnosis and overtreatment; programmes for early detection of invasive lung cancers are emerging, and have faced similar challenges. A crucial consideration in screening for breast, prostate, and lung cancers is their remarkable phenotypic heterogeneity, ranging from indolent to highly aggressive. Efforts have been made to address the limitations of cancer-screening programmes, providing an opportunity for cross-disciplinary learning and further advancement of the science. Current innovations are aimed at identifying the individuals who are most likely to benefit from screening, increasing the yield of consequential cancers on screening and biopsy, and using molecular tests to improve our understanding of disease biology and to tailor treatment. We discuss each of these concepts and outline a dynamic framework for continuous improvements in the field of cancer screening. |
Audience | Academic |
Author | Kramer, Barnett S. Sawaya, George F. Eklund, Martin Esserman, Laura J. Black, William C. Shieh, Yiwey |
AuthorAffiliation | 4 Department of Radiology, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, 1 Medical Center Drive, Lebanon, New Hampshire 03756, USA 6 Departments of Surgery and Radiology, University of California, San Francisco, 1600 Divisadero Street, Box 1710, San Francisco, California 94115, USA 3 Departments of Obstetrics, Gynecology, and Reproductive Sciences, School of Medicine, University of California, San Francisco, 550 16th Street, San Francisco, California 94158, USA 2 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels väg 12A, 17177 Stockholm, Sweden 1 Division of General Internal Medicine, Department of Medicine, University of California, San Francisco, 1545 Divisadero Street, San Francisco, California 94115, USA 5 Division of Cancer Prevention, National Cancer Institute, 9609 Medical Center Drive, Bethesda, Maryland 20892, USA |
AuthorAffiliation_xml | – name: 4 Department of Radiology, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center, 1 Medical Center Drive, Lebanon, New Hampshire 03756, USA – name: 5 Division of Cancer Prevention, National Cancer Institute, 9609 Medical Center Drive, Bethesda, Maryland 20892, USA – name: 1 Division of General Internal Medicine, Department of Medicine, University of California, San Francisco, 1545 Divisadero Street, San Francisco, California 94115, USA – name: 2 Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Nobels väg 12A, 17177 Stockholm, Sweden – name: 3 Departments of Obstetrics, Gynecology, and Reproductive Sciences, School of Medicine, University of California, San Francisco, 550 16th Street, San Francisco, California 94158, USA – name: 6 Departments of Surgery and Radiology, University of California, San Francisco, 1600 Divisadero Street, Box 1710, San Francisco, California 94115, USA |
Author_xml | – sequence: 1 givenname: Yiwey surname: Shieh fullname: Shieh, Yiwey organization: Division of General Internal Medicine, Department of Medicine, University of California, San Francisco – sequence: 2 givenname: Martin surname: Eklund fullname: Eklund, Martin organization: Department of Medical Epidemiology and Biostatistics, Karolinska Institutet – sequence: 3 givenname: George F. surname: Sawaya fullname: Sawaya, George F. organization: Departments of Obstetrics, Gynecology, and Reproductive Sciences, School of Medicine, University of California, San Francisco – sequence: 4 givenname: William C. surname: Black fullname: Black, William C. organization: Department of Radiology, Geisel School of Medicine at Dartmouth, Dartmouth-Hitchcock Medical Center – sequence: 5 givenname: Barnett S. surname: Kramer fullname: Kramer, Barnett S. organization: Division of Cancer Prevention, National Cancer Institute – sequence: 6 givenname: Laura J. surname: Esserman fullname: Esserman, Laura J. email: laura.esserman@ucsfmedctr.org organization: Departments of Surgery and Radiology, University of California, San Francisco |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/27071351$$D View this record in MEDLINE/PubMed http://kipublications.ki.se/Default.aspx?queryparsed=id:134144758$$DView record from Swedish Publication Index |
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PublicationPlace | London |
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PublicationTitle | Nature reviews. Clinical oncology |
PublicationTitleAbbrev | Nat Rev Clin Oncol |
PublicationTitleAlternate | Nat Rev Clin Oncol |
PublicationYear | 2016 |
Publisher | Nature Publishing Group UK Nature Publishing Group |
Publisher_xml | – name: Nature Publishing Group UK – name: Nature Publishing Group |
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Tumours within any organ site can have a spectrum of biological phenotypes, ranging from indolent to highly aggressive
Screening for cancer is most... Several important lessons have been learnt from our experiences in screening for various cancers. Screening programmes for cervical and colorectal cancers have... |
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Title | Population-based screening for cancer: hope and hype |
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