Genomic Classifier ColoPrint Predicts Recurrence in Stage II Colorectal Cancer Patients More Accurately Than Clinical Factors

被引:101
作者
Kopetz, Scott [1 ]
Tabernero, Josep [3 ,4 ]
Rosenberg, Robert [5 ]
Jiang, Zhi-Qin [1 ]
Moreno, Victor [6 ,7 ]
Bachleitner-Hofmann, Thomas [8 ]
Lanza, Giovanni [9 ]
Stork-Sloots, Lisette [10 ,11 ]
Maru, Dipen [2 ]
Simon, Iris [10 ,11 ]
Capella, Gabriel [6 ]
Salazar, Ramon [6 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Gastrointestinal Med Oncol, Unit 426, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[3] Univ Autonoma Barcelona, Vall Hebron Univ Hosp, E-08193 Barcelona, Spain
[4] Univ Autonoma Barcelona, Inst Oncol, E-08193 Barcelona, Spain
[5] Tech Univ Munich, Klinikum Rechts Isar, Dept Surg, D-80290 Munich, Germany
[6] IDIBELL Hosp Llobregat, Inst Catala Oncol, Barcelona, Spain
[7] Univ Barcelona, Fac Med, Dept Clin Sci, Barcelona 7, Spain
[8] Med Univ Vienna, Dept Surg, Vienna, Austria
[9] Univ Ferrara, Dept Surg, I-44100 Ferrara, Italy
[10] Agendia NV, Amsterdam, Netherlands
[11] Agendia Inc, Irvine, CA USA
关键词
Stage II colon cancer; Risk prediction; Gene expression signature; Risk classification; COLON-CANCER; ADJUVANT CHEMOTHERAPY; BREAST-CANCER; PROGNOSIS; THERAPY;
D O I
10.1634/theoncologist.2014-0325
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Approximately 20% of patients with stage II colorectal cancer will experience a relapse. Current clinicalpathologic stratification factors do not allowclear identification of these high-risk patients. ColoPrint (Agendia, Amsterdam, The Netherlands, http://www.agendia.com) is a gene expression classifier that distinguishes patients with low or high risk of disease relapse. Methods. ColoPrint was developed using whole-genome expression data and validated in several independent validation cohorts. Stage II patients from these studies were pooled (n = 416), and ColoPrint was compared with clinical risk factors described in the National Comprehensive Cancer Network (NCCN) 2013 Guidelines for Colon Cancer. Median follow-up was 81 months. Most patients (70%) did not receive adjuvant chemotherapy. Risk of relapse (ROR) was defined as survival until first event of recurrence or death from cancer. Results. In the pooled stage II data set, ColoPrint identified 63% of patients as low risk with a 5-year ROR of 10%, whereas high-risk patients (37%) had a 5-year ROR of 21%, with a hazard ratio (HR) of 2.16 (p = .004). This remained significant in a multivariate model that included number of lymph nodes retrieved and microsatellite instability. In the T3 microsatellite-stable subgroup (n = 301), ColoPrint classified 59% of patients as low risk with a 5-year ROR of 9.9%. High-risk patients (31%) had a 22.4% ROR (HR: 2.41; p = .005). In contrast, the NCCN clinical high-risk factors were unable to distinguish high-and low-risk patients (15% vs. 13% ROR; p = .55). Conclusion. ColoPrint significantly improved prognostic accuracy independent of microsatellite status or clinical variables, facilitating the identification of patients at higher risk who might be considered for additional treatment.
引用
收藏
页码:127 / 133
页数:7
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