Methods for etiologic and early marker investigations in the PLCO trial

Richard B. Hayes, Alice Sigurdson, Lee Moore, Ulrike Peters, Wen Yi Huang, Paul Pinsky, Douglas Reding, Edward P. Gelmann, Nat Rothman, Ruth M. Pfeiffer, Robert N. Hoover, Christine D. Berg

Research output: Contribution to journalArticlepeer-review

122 Scopus citations

Abstract

With the rapid development of biomarkers and new technologies, large-scale biologically-based cohort studies present expanding opportunities for population-based research on disease etiology and early detection markers. The prostate, lung, colorectal and ovarian cancer (PLCO) screening trial is a large randomized trial designed to determine if screening for these cancers leads to mortality reduction for these diseases. Within the Trial, the PLCO etiology and early marker study (EEMS) identifies risk factors for cancer and other diseases and evaluates biologic markers for the early detection of disease. EEMS includes 155,000 volunteers who provide basic risk factor information. Serial blood samples are collected at each of six screening rounds (including one collection for cryopreserved whole blood) from screening arm participants (77,000 subjects) and buccal cells are collected from those in the control arm of the trial. Etiologic studies consider environmental (e.g., diet), biochemical, and genetic factors. Early detection studies focus on blood-based biologic markers of early disease. Clinical epidemiology is also an important component of the PLCO trial.

Original languageEnglish (US)
Pages (from-to)147-154
Number of pages8
JournalMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
Volume592
Issue number1-2
DOIs
StatePublished - Dec 30 2005
Externally publishedYes

Keywords

  • Cancer
  • Cohort
  • Molecular epidemiology

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Health, Toxicology and Mutagenesis

Fingerprint

Dive into the research topics of 'Methods for etiologic and early marker investigations in the PLCO trial'. Together they form a unique fingerprint.

Cite this