Aspirin and COX-2 inhibitor use in patients with stage III colon cancer

Kimmie Ng*, Jeffrey A. Meyerhardt, Andrew T. Chan, Kaori Sato, Jennifer A. Chan, Donna Niedzwiecki, Leonard B. Saltz, Robert J. Mayer, Al B. Benson, Paul L. Schaefer, Renaud Whittom, Alexander Hantel, Richard M. Goldberg, Alan P. Venook, Shuji Ogino, Edward L. Giovannucci, Charles S. Fuchs

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

124 Scopus citations

Abstract

We conducted a prospective, observational study of aspirin and COX-2 inhibitor use and survival in stage III colon cancer patients enrolled in an adjuvant chemotherapy trial. Among 799 eligible patients, aspirin use was associated with improved recurrence-free survival (RFS) (multivariable hazard ratio [HR] = 0.51, 95% confidence interval [CI] = 0.28 to 0.95), disease-free survival (DFS) (HR = 0.68, 95% CI = 0.42 to 1.11), and overall survival (OS) (HR = 0.63, 95% CI = 0.35 to 1.12). Adjusted HRs for DFS and OS censored at five years (in an attempt to minimize misclassification from noncancer death) were 0.61 (95% CI = 0.36 to 1.04) and 0.48 (95% CI = 0.23 to 0.99). Among 843 eligible patients, those who used COX-2 inhibitors had multivariable HRs for RFS, DFS, and OS of 0.53 (95% CI = 0.27 to 1.04), 0.60 (95% CI = 0.33 to 1.08), and 0.50 (95% CI = 0.23 to 1.07), and HRs of 0.47 (95% CI = 0.24 to 0.91) and 0.26 (95% CI = 0.08 to 0.81) for DFS and OS censored at five years. Aspirin and COX-2 inhibitor use may be associated with improved outcomes in stage III colon cancer patients.

Original languageEnglish (US)
JournalJournal of the National Cancer Institute
Volume107
Issue number1
DOIs
StatePublished - Jan 1 2015

Funding

This work was supported by the National Cancer Institute, National Institutes of Health (P50 CA127003 and K07 CA148894 to KN), the Conquer Cancer Foundation of the American Society of Clinical Oncology (to KN), the Damon Runyan Cancer Research Foundation (to ATC), and the Pharmacia and Upjohn Company, now Pfizer Oncology. The research for CALGB 89803 was also supported, in part, by grants from the National Cancer Institute, National Institutes of Health (CA31946) to the Alliance for Clinical Trials in Oncology (Monica Bertagnolli, MD, Chairman) and to the Alliance Statistics and Data Center (Daniel J. Sargent, PhD, CA33601).

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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