CpG Island Methylator Phenotype Is Associated With Response to Adjuvant Irinotecan-Based Therapy for Stage III Colon Cancer

被引:115
作者
Shiovitz, Stacey [1 ,2 ]
Bertagnolli, Monica M. [3 ,4 ]
Renfro, Lindsay A. [5 ]
Nam, Eunmi [6 ]
Foster, Nathan R. [5 ]
Dzieciatkowski, Slavomir [2 ]
Luo, Yanxin [2 ,7 ]
Lao, Victoria Valinluck [2 ,8 ]
Monnat, Raymond J., Jr. [9 ,10 ]
Emond, Mary J. [11 ]
Maizels, Nancy [12 ,13 ]
Niedzwiecki, Donna [14 ]
Goldberg, Richard M. [15 ]
Saltz, Leonard B. [16 ]
Venook, Alan [17 ,18 ]
Warren, Robert S. [17 ,18 ]
Grady, William M. [1 ,2 ]
机构
[1] Univ Washington, Dept Med, Seattle, WA USA
[2] Fred Hutchinson Canc Res Ctr, Clin Res Div, Seattle, WA 98109 USA
[3] Dana Farber Canc Inst, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Boston, MA 02115 USA
[5] Mayo Clin, Alliance Stat & Data Ctr, Rochester, MN USA
[6] Ewha Womans Univ, Sch Med, Div Hematol Oncol, Seoul, South Korea
[7] Sun Yat Sen Univ, Affiliated Hosp 6, Dept Colorectal Surg, Guangzhou, Guangdong, Peoples R China
[8] Univ Washington, Sch Med, Dept Surg, Seattle, WA 98195 USA
[9] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98195 USA
[10] Univ Washington, Sch Med, Dept Genome Sci, Seattle, WA USA
[11] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[12] Univ Washington, Dept Immunol, Seattle, WA 98195 USA
[13] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[14] Duke Univ, Med Ctr, Alliance Stat & Data Ctr, Durham, NC USA
[15] Ohio State Univ, Columbus, OH 43210 USA
[16] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[17] Univ Calif San Francisco, San Francisco, CA 94143 USA
[18] Helen Diller Family Comprehens Canc Ctr, San Francisco, CA USA
基金
美国国家卫生研究院;
关键词
CALGB (Alliance) 89803; CRC; Epigenetic Factors; Chemotherapy; TRIAL CALGB 89803; COLORECTAL-CANCER; MICROSATELLITE INSTABILITY; CLINICAL-PRACTICE; SURVIVAL BENEFIT; DNA METHYLATION; RECQ HELICASES; BRAF MUTATION; FLUOROURACIL; CHEMOTHERAPY;
D O I
10.1053/j.gastro.2014.05.009
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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.
引用
收藏
页码:637 / 645
页数:9
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