Gene expression profile predictive of response to chemotherapy in metastatic colorectal cancer

被引:23
|
作者
Estevez-Garcia, Purificacion [1 ,2 ]
Rivera, Fernando [3 ]
Molina-Pinelo, Sonia [1 ]
Benavent, Marta [1 ,2 ]
Gomez, Javier [4 ]
Luisa Limon, Maria [2 ]
Dolores Pastor, Maria [1 ]
Martinez-Perez, Julia [1 ,2 ]
Paz-Ares, Luis [1 ,2 ]
Carnero, Amancio [5 ]
Garcia-Carbonero, Rocio [1 ,2 ]
机构
[1] Univ Seville, CSIC, Inst Biomed Sevilla IBIS, Lab Oncol Mol & Nuevas Terapias,HUVR, Seville, Spain
[2] Hosp Univ Virgen del Rocio, Med Oncol Dept, Seville, Spain
[3] Hosp Univ Marques de Valdecilla, Med Oncol Dept, Santander, Spain
[4] Hosp Univ Marques de Valdecilla, Dept Pathol, Santander, Spain
[5] Univ Seville, CSIC, Inst Biomed Sevilla IBIS, Lab Biol Mol Canc,HUVR, Seville, Spain
关键词
Colorectal cancer; chemotherapy; gene expression; predictive; microarray; COLON; RECURRENCE; GUIDELINES; SIGNATURE; FLUOROURACIL; VALIDATION; ASSAY; RISK; OXALIPLATIN; LEUCOVORIN;
D O I
10.18632/oncotarget.3152
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Fluoropyrimidine-based chemotherapy (CT) has been the mainstay of care of metastatic colorectal cancer (mCRC) for years. Response rates are only observed, however, in about half of treated patients, and there are no reliable tools to prospectively identify patients more likely to benefit from therapy. The purpose of our study was to identify a gene expression profile predictive of CT response in mCRC. Whole genome expression analyses (Affymetrix GeneChip r HG-U133 Plus 2.0) were performed in fresh frozen tumor samples of 37 mCRC patients (training cohort). Differential gene expression profiles among the two study conditions (responders versus non-responders) were assessed using supervised class prediction algorithms. A set of 161 differentially expressed genes in responders (23 patients; 62%) versus non-responders (14 patients; 38%) was selected for further assessment and validation by RT-qPCR (TaqMan (R) Low Density Arrays (TLDA) 7900 HT Micro Fluidic Cards) in an independent multi-institutional cohort (53 mCRC patients). Seven of these genes were confirmed as significant predictors of response. Patients with a favorable predictive signature had significantly greater response rate (58% vs 13%, p = 0.024), progression-free survival (61% vs 13% at 1 year, HR = 0.32, p = 0.009) and overall survival (32 vs 16 months, HR = 0.21, p = 0.003) than patients with an unfavorable gene signature. This is the first study to validate a gene-expression profile predictive of response to CT in mCRC patients. Larger and prospective confirmatory studies are required, however, in order to successfully provide oncologists with adequate tools to optimize treatment selection in routine clinical practice.
引用
收藏
页码:6151 / 6159
页数:9
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