Your browser doesn't support javascript.
loading
Research Needs for Understanding the Biology of Overdiagnosis in Cancer Screening.
Srivastava, Sudhir; Reid, Brian J; Ghosh, Sharmistha; Kramer, Barnett S.
Afiliação
  • Srivastava S; Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Reid BJ; Divisions of Human Biology and Public Health Sciences, Fred Hutchinson Cancer Research Center, Departments of Genome Sciences and Medicine, University of Washington, Seattle, Washington.
  • Ghosh S; Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
  • Kramer BS; Division of Cancer Prevention, National Cancer Institute, National Institutes of Health, Bethesda, Maryland.
J Cell Physiol ; 231(9): 1870-5, 2016 09.
Article em En | MEDLINE | ID: mdl-26505642
ABSTRACT
Many cancers offer an extended window of opportunity for early detection and therapeutic intervention that could lead to a reduction in cause-specific mortality. The pursuit of early detection in screening settings has resulted in decreased incidence and mortality for some cancers (e.g., colon and cervical cancers), and increased incidence with only modest or no effect on cause-specific mortality in others (e.g., breast and prostate). Whereas highly sensitive screening technologies are better at detecting a number of suspected "cancers" that are indolent and likely to remain clinically unimportant in the lifetime of a patient, defined as overdiagnosis, they often miss cancers that are aggressive and tend to present clinically between screenings, known as interval cancers. Unrecognized overdiagnosis leads to overtreatment with its attendant (often long-lasting) side effects, anxiety, and substantial financial harm. Existing methods often cannot differentiate indolent lesions from aggressive ones or understand the dynamics of neoplastic progression. To correctly identify the population that would benefit the most from screening and identify the lesions that would benefit most from treatment, the evolving genomic and molecular profiles of individual cancers during the clinical course of progression or indolence must be investigated, while taking into account an individual's genetic susceptibility, clinical and environmental risk factors, and the tumor microenvironment. Practical challenges lie not only in the lack of access to tissue specimens that are appropriate for the study of natural history, but also in the absence of targeted research strategies. This commentary summarizes the recommendations from a diverse group of scientists with expertise in basic biology, translational research, clinical research, statistics, and epidemiology and public health professionals convened to discuss research directions. J. Cell. Physiol. 231 1870-1875, 2016. © 2015 Wiley Periodicals, Inc.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Programas de Rastreamento / Predisposição Genética para Doença / Detecção Precoce de Câncer / Uso Excessivo dos Serviços de Saúde / Neoplasias Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Programas de Rastreamento / Predisposição Genética para Doença / Detecção Precoce de Câncer / Uso Excessivo dos Serviços de Saúde / Neoplasias Tipo de estudo: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Animals / Humans Idioma: En Ano de publicação: 2016 Tipo de documento: Article