CpG island methylator phenotype is associated with response to adjuvant irinotecan-based therapy for stage III colon cancer Journal Article


Authors: Shiovitz, S.; Bertagnolli, M. M.; Renfro, L. A.; Nam, E.; Foster, N. R.; Dzieciatkowski, S.; Luo, Y.; Lao, V. V.; Monnat, R. J. Jr; Emond, M. J.; Maizels, N.; Niedzwiecki, D.; Goldberg, R. M.; Saltz, L. B.; Venook, A.; Warren, R. S.; Grady, W. M.
Article Title: CpG island methylator phenotype is associated with response to adjuvant irinotecan-based therapy for stage III colon cancer
Abstract: Background & Aims The CpG island methylator phenotype (CIMP), defined by a high frequency of aberrantly methylated genes, is a characteristic of a subclass of colon tumors with distinct clinical and molecular features. Cohort studies have produced conflicting results on responses of CIMP-positive tumors to chemotherapy. We assessed the association between tumor CIMP status and survival of patients receiving adjuvant fluorouracil and leucovorin alone or with irinotecan (IFL). Methods We analyzed data from patients with stage III colon adenocarcinoma randomly assigned to groups given fluorouracil and leucovorin or IFL after surgery, from April 1999 through April 2001. The primary end point of the trial was overall survival and the secondary end point was disease-free survival. DNA isolated from available tumor samples (n = 615) was used to determine CIMP status based on methylation patterns at the CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1 loci. The effects of CIMP on survival were modeled using Kaplan-Meier and Cox proportional hazards; interactions with treatment and BRAF, KRAS, and mismatch repair (MMR) status were also investigated. Results Of the tumor samples characterized for CIMP status, 145 were CIMP positive (23%). Patients with CIMP-positive tumors had shorter overall survival times than patients with CIMP-negative tumors (hazard ratio = 1.36; 95% confidence interval: 1.01-1.84). Treatment with IFL showed a trend toward increased overall survival for patients with CIMP-positive tumors, compared with treatment with fluorouracil and leucovorin (hazard ratio = 0.62; 95% CI: 0.37-1.05; P =.07), but not for patients with CIMP-negative tumors (hazard ratio = 1.38; 95% CI: 1.00-1.89; P =.049). In a 3-way interaction analysis, patients with CIMP-positive, MMR-intact tumors benefited most from the addition of irinotecan to fluorouracil and leucovorin therapy (for the interaction, P =.01). CIMP was more strongly associated with response to IFL than MMR status. Results for disease-free survival times were comparable among all analyses. Conclusions Patients with stage III, CIMP-positive, MMR-intact colon tumors have longer survival times when irinotecan is added to combination therapy with fluorouracil and leucovorin. © 2014 by the AGA Institute.
Keywords: adult; controlled study; aged; major clinical study; overall survival; fluorouracil; monotherapy; cancer adjuvant therapy; disease free survival; chemotherapy; cancer staging; follow up; phenotype; multiple cycle treatment; randomized controlled trial; cohort analysis; irinotecan; survival time; add on therapy; cpg island; folinic acid; mismatch repair; phase 3 clinical trial; k ras protein; colon adenocarcinoma; b raf kinase; somatomedin b; dna isolation; suppressor of cytokine signaling 1; neurogenin 1; human; male; female; priority journal; article; transcription factor runx3; calgb (alliance) 89803; crc; epigenetic factors; cpg island methylator phenotype
Journal Title: Gastroenterology
Volume: 147
Issue: 3
ISSN: 0016-5085
Publisher: Elsevier Inc.  
Date Published: 2014-09-01
Start Page: 637
End Page: 645
Language: English
DOI: 10.1053/j.gastro.2014.05.009
PROVIDER: scopus
PMCID: PMC4143495
PUBMED: 24859205
DOI/URL:
Notes: Export Date: 1 October 2014 -- Source: Scopus
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  1. Leonard B Saltz
    790 Saltz