A transcriptomic signature that predicts cancer recurrence after hepatectomy in patients with colorectal liver metastases

被引:9
|
作者
Wada, Yuma [1 ,2 ,3 ,4 ]
Shimada, Mitsuo [2 ]
Morine, Yuji [2 ]
Ikemoto, Tetsuya [2 ]
Saito, Yu [2 ]
Baba, Hideo [5 ]
Mori, Masaki [6 ]
Goel, Ajay [1 ,3 ,4 ]
机构
[1] City Hope Comprehens Canc Ctr, Dept Mol Diagnost & Expt Therapeut, Beckman Res Inst, Duarte, CA USA
[2] Tokushima Univ, Dept Surg, Tokushima, Japan
[3] Baylor Univ, Ctr Gastrointestinal Res, Baylor Scott & White Res Inst, Med Ctr, Dallas, TX USA
[4] Baylor Univ, Med Ctr, Charles Sammons Canc Ctr, Dallas, TX USA
[5] Kumamoto Univ, Grad Sch Med Sci, Dept Gastroenterol Surg, Kumamoto, Japan
[6] Kyushu Univ, Grad Sch Med Sci, Dept Surg & Sci, Fukuoka, Japan
基金
美国国家卫生研究院;
关键词
Gene signature; Genome-wide profiling; Risk-stratification; Prediction biomarker; Tissue-based identification; PROGNOSTIC-FACTORS; 1ST-LINE TREATMENT; HEPATIC RESECTION; GENE-EXPRESSION; BRAF MUTATION; PHASE-III; CHEMOTHERAPY; SURVIVAL; SURGERY; FOLFOX4;
D O I
10.1016/j.ejca.2021.12.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Cancer recurrence is an important predictor of survival outcomes in patients with colorectal cancer-associated liver metastasis (CRLM), who undergo radical hepatectomy. Therefore, identification of patients with the greatest risk of recurrence is critical for developing a precision oncology strategy that might include frequent surveillance (in low-risk patients) or a more aggressive treatment approach (in high-risk patients). We performed genome-wide expression profiling, to identify and develop a transcriptomic signature for predicting recurrence in patients with CRLM.Methods: We analysed a total of 383 patients with CRLM, including 63 patients from a publicly available data set (the NCBI's Gene Expression Omnibus with accession number GSE81423). and 320 patients from whom surgical specimens were collected for independent training (n = 169) and validation (n = 151) of identified biomarkers. Using C ox's proportional hazard regression analysis, we evaluated the clinical significance of the identified gene signature by comparing its performance with several key clinical factors.Results: We identified a six-gene panel that robustly categorised patients with recurrence in the discovery (area under the curve (AUC) = 0.90). We showed that the panel was a significant predictor of recurrence in the clinical training (AUC = 0.83) and validation cohorts (AUC = 0.81). By combining our panel with key clinical factors, we established a risk stratification model that emerged as an independent predictor of recurrence (AUC = 0.85; univariate: hazard ratio (HR) = 4.34, 95% confidence interval (CI) = 2.71-6.93, P < 0.001; multivariate: HR = 3.40, 95% CI = 1.76-6.56, P < 0.001). The stratification model revealed recurrence prediction in 89% of high-risk group and non-recurrence in 62% of low-risk group.Conclusions: We established a novel transcriptomic signature that robustly predicts recurrence, which has significant implications for the management of patients with CRLM.(c) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:66 / 76
页数:11
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