University of Hertfordshire

From the same journal

By the same authors

  • Darragh P O'Brien
  • Neomal S Sandanayake
  • Claire Jenkinson
  • Aleksandra Gentry-Maharaj
  • Sophia Apostolidou
  • Evangelia-Ourania Fourkala
  • Richard Gunu
  • Stephane Camuzeaux
  • Oleg Blyuss
  • Anne Dawnay
  • Alexey Zaikin
  • Ross C Smith
  • Ian J Jacobs
  • Usha Menon
  • Eithne Costello
  • Stephen P Pereira
  • John F Timms
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Original languageEnglish
Pages (from-to)622-31
Number of pages10
JournalClinical Cancer Research
Volume21
Issue3
DOIs
Publication statusPublished - 1 Feb 2015

Abstract

PURPOSE: Biomarkers for the early detection of pancreatic cancer are urgently needed. The primary objective of this study was to evaluate whether increased levels of serum CA19-9, CA125, CEACAM1, and REG3A are present before clinical presentation of pancreatic cancer and to assess the performance of combined markers for early detection and prognosis.

EXPERIMENTAL DESIGN: This nested case-control study within the UKCTOCS included 118 single and 143 serial serum samples from 154 postmenopausal women who were subsequently diagnosed with pancreatic cancer and 304 matched noncancer controls. Samples were split randomly into independent training and test sets. CA19-9, CA125, CEACAM1, and REG3A were measured using ELISA and/or CLIA. Performance of markers to detect cancers at different times before diagnosis and for prognosis was evaluated.

RESULTS: At 95% specificity, CA19-9 (>37 U/mL) had a sensitivity of 68% up to 1 year, and 53% up to 2 years before diagnosis. Combining CA19-9 and CA125 improved sensitivity as CA125 was elevated (>30 U/mL) in approximately 20% of CA19-9-negative cases. CEACAM1 and REG3A were late markers adding little in combined models. Average lead times of 20 to 23 months were estimated for test-positive cases. Prediagnostic levels of CA19-9 and CA125 were associated with poor overall survival (HR, 2.69 and 3.15, respectively).

CONCLUSIONS: CA19-9 and CA125 have encouraging sensitivity for detecting preclinical pancreatic cancer, and both markers can be used as prognostic tools. This work challenges the prevailing view that CA19-9 is upregulated late in the course of pancreatic cancer development.

Notes

©2014 American Association for Cancer Research.

ID: 18771237