Elevated pretreatment CEA and CA19-9 levels are related to early treatment failure in esophageal adenocarcinoma

Rosa T. Van Der Kaaij*, Francine E.M. Voncken, Jolanda M. Van Dieren, Petur Snaebjornsson, Catharina M. Korse, Cecile Grootscholten, Berthe M.P. Aleman, Johanna W. Van Sandick

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

Introduction: Chemoradiotherapy and surgery are the basis of the potentially curative treatment for esophageal cancer. Approximately 1 in 5 patients, however, do not benefit from this intensive treatment due to early treatment failure. The aim of this study was to evaluate levels of carcinoembryonic antigen (CEA) and carbohydrate antigen (CA) 19-9 at diagnosis, in relation to survival and early treatment failure (disease recurrence or death within 1 year after surgery). Methods: Patients with esophageal adenocarcinoma scheduled for chemoradiotherapy followed by surgery between 1998 and 2014 were selected from a retrospectively collected database if both CEA and CA19-9 levels were measured before the start of treatment. Results: Pretreatment CEA and CA19-9 levels were known in 102 patients. Median overall survival differed (P<0.001) between patients with normal levels of both CEA and CA19-9 (n=59; 51 mo), patients with elevated CEA only (n=13; 43 mo), patients with elevated CA19-9 only (n=19; 24 mo), and those with elevated levels of both CEA and CA19-9 (n= 11; 11 mo). Elevation of both CEA and CA19-9 was associated with early treatment failure (odds ratio: 10.4; 95% confidence interval: 2.4-45.5, P= 0.002). Median time to tumor recurrence was 34 months in patients with normal CEA and CA19-9 levels, and 7 months in those with elevated levels of both (P=0.003). Conclusions: Pretreatment elevated CEA and CA19-9 levels were significantly associated with early treatment failure and decreased overall survival in this esophageal adenocarcinoma patient cohort treated with curative intent. Until prospective validation, CEA and CA19-9 might play a role in identifying high-risk patients before the start of intensive locoregional therapy.

Original languageEnglish
Pages (from-to)345-350
Number of pages6
JournalAmerican Journal of Clinical Oncology: Cancer Clinical Trials
Volume42
Issue number4
DOIs
Publication statusPublished - 1 Apr 2019

Bibliographical note

Funding Information:
From the Departments of *Surgical Oncology; †Radiation Oncology; ‡Gastroenterology; §Pathology; ∥Clinical Chemistry; and ¶Medical Oncology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Amsterdam, the Netherlands. R.T.V.D.K. and F.E.M.V. contributed equally. This research was funded by the Cornelis Vrolijk Development Fund. The authors declare no conflicts of interest. Reprints: Rosa T. van der Kaaij, MD, PhD, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands. E-mail: [email protected]. Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved. ISSN: 0277-3732/19/4204-0345 DOI: 10.1097/COC.0000000000000525

Publisher Copyright:
Copyright © 2019 Wolters Kluwer Health, Inc. All rights reserved.

Other keywords

  • Adenocarcinoma
  • CA19-9
  • CEA
  • Esophageal neoplasms
  • Neoadjuvant chemoradiotherapy
  • Prognosis
  • Survival
  • Tumor markers

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