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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Summary: | 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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 All authors researched the data for article, contributed substantially to discussions of content and reviewed/edited the manuscript before submission. Y.S. and L.J.E. wrote the manuscript. Author contributions |
ISSN: | 1759-4774 1759-4782 |
DOI: | 10.1038/nrclinonc.2016.50 |