Ann Coloproctol.  2015 Jun;31(3):92-97. 10.3393/ac.2015.31.3.92.

ERCC1 as a Predictive Marker for FOLFOX Chemotherapy in an Adjuvant Setting

Affiliations
  • 1Department of Surgery, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea. bkbsur@yahoo.co.kr
  • 2Department of Internal Medicine, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • 3Department of Pathology, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.
  • 4Clinical Trial Center in Pharmacology, Inje University Busan Paik Hospital, Inje University College of Medicine, Busan, Korea.

Abstract

PURPOSE
The purpose of this study was to identify the excision repair cross-complementation group 1 (ERCC1) as a predictive marker for FOLFOX adjuvant chemotherapy in stages II and III colon cancer patients.
METHODS
A total of 166 high risk stages II and III colon cancer patients were retrospectively enrolled in this study, and data were collected prospectively. They underwent a curative resection followed by FOLFOX4 adjuvant chemotherapy. We analyzed ERCC1 expression in the primary colon tumor by using immunohistochemical staining. The oncological outcomes included the 5-year disease-free survival (DFS) rate. The DFS was analyzed by using the Kaplan-Meier method with the log-rank test. A Cox proportional hazard model was used for the prognostic analysis.
RESULTS
ERCC1-positive expression was statistically significant in the older patients (P = 0.032). In the multivariate analysis, the prognostic factors for DFS were female sex (P = 0.016), N stage (P = 0.009), and postoperative carcinoembryonic antigen level (P = 0.001), but ERCC1 expression was not a statistically significant prognostic factor for DFS in the univariate analysis (P = 0.397). The 5-year DFS rate was not significantly associated with the ERCC1 expression in all patients (P = 0.396) or with stage III disease (P = 0.582).
CONCLUSION
We found that ERCC1 expression was not significantly correlated with the 5-year DFS as reflected by the oncologic outcomes in patients with high-risk stages II and III colon cancer treated with FOLFOX adjuvant chemotherapy.

Keyword

Colon neoplasms; FOLFOX; ERCC1

MeSH Terms

Carcinoembryonic Antigen
Chemotherapy, Adjuvant
Colon
Colonic Neoplasms
Disease-Free Survival
DNA Repair
Drug Therapy*
Female
Humans
Multivariate Analysis
Proportional Hazards Models
Prospective Studies
Retrospective Studies
Carcinoembryonic Antigen
Full Text Links
  • AC
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr