ClearCode34: A Prognostic Risk Predictor for Localized Clear Cell Renal Cell Carcinoma

被引:225
作者
Brooks, Samira A. [1 ]
Brannon, A. Rose [1 ,2 ]
Parker, Joel S. [1 ]
Fisher, Jennifer C. [1 ]
Sen, Oishee [1 ]
Kattan, Michael W. [1 ,3 ]
Hakimi, A. Ari [4 ]
Hsieh, James J. [4 ]
Choueiri, Toni K. [5 ,6 ]
Tamboli, Pheroze
Maranchie, Jodi K. [7 ]
Hinds, Peter [7 ]
Miller, C. Ryan [1 ,8 ]
Nielsen, Matthew E. [1 ,9 ,10 ]
Rathmell, W. Kimryn [1 ,11 ,12 ]
机构
[1] Univ N Carolina, Lineberger Canc Ctr, Chapel Hill, NC 27599 USA
[2] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[3] Cleveland Clin, Dept Quantitat Hlth Sci, Cleveland, OH 44106 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Surg, Urol Serv, New York, NY 10021 USA
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA USA
[6] Dana Farber Canc Inst, Kidney Canc Ctr, Boston, MA USA
[7] Univ Texas Houston, MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[8] Univ N Carolina, Dept Pathol, Chapel Hill, NC USA
[9] Univ N Carolina, Dept Urol, Chapel Hill, NC USA
[10] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC USA
[11] Univ N Carolina, Dept Med, Div Hematol & Oncol, Chapel Hill, NC USA
[12] Univ N Carolina, Dept Genet, Chapel Hill, NC USA
基金
美国国家卫生研究院;
关键词
Biomarker; ccRCC; Kidney cancer; Renal cell carcinoma; TCGA; Prognosis; GENE-EXPRESSION; BREAST-CANCER; CLASSIFICATION;
D O I
10.1016/j.eururo.2014.02.035
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
100201 [内科学]; 100221 [泌尿外科学];
摘要
Background: Gene expression signatures have proven to be useful tools in many cancers to identify distinct subtypes of disease based on molecular features that drive pathogenesis, and to aid in predicting clinical outcomes. However, there are no current signatures for kidney cancer that are applicable in a clinical setting. Objective: To generate a signature biomarker for the clear cell renal cell carcinoma (ccRCC) good risk (ccA) and poor risk (ccB) subtype classification that could be readily applied to clinical samples to develop an integrated model for biologically defined risk stratification. Design, setting, and participants: A set of 72 ccRCC sample standards was used to develop a 34-gene classifier (ClearCode34) for assigning ccRCC tumors to subtypes. The classifier was applied to RNA-sequencing data from 380 nonmetastatic ccRCC samples from the Cancer Genome Atlas (TCGA), and to 157 formalin-fixed clinical samples collected at the University of North Carolina. Outcome measurements and statistical analysis: Kaplan-Meier analyses were performed on the individual cohorts to calculate recurrence-free survival (RFS), cancer-specific survival (CSS), and overall survival (OS). Training and test sets were randomly selected from the combined cohorts to assemble a risk prediction model for disease recurrence. Results and limitations: The subtypes were significantly associated with RFS (p < 0.01), CSS (p < 0.01), and OS (p < 0.01). Hazard ratios for subtype classification were similar to those of stage and grade in association with recurrence risk, and remained significant in multivariate analyses. An integrated molecular/clinical model for RFS to assign patients to risk groups was able to accurately predict CSS above established, clinical risk-prediction algorithms. Conclusions: The ClearCode34-based model provides prognostic stratification that improves upon established algorithms to assess risk for recurrence and death for nonmetastatic ccRCC patients. Patient summary: We developed a 34-gene subtype predictor to classify clear cell renal cell carcinoma tumors according to ccA or ccB subtypes and built a subtype-inclusive model to analyze patient survival outcomes. (C) 2014 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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