BRAF mutation is a prognostic biomarker for colorectal liver metastasectomy

Hao Wei Teng, Yu Chung Huang, Jen Kou Lin, Wei Shone Chen, Tzu Chen Lin, Jeng Kai Jiang, Chueh Chuan Yen, Anna Fen Yau Li, Hsei Wei Wang, Shih Ching Chang, Yuan Tzu Lan, Chun Chi Lin, Huann Sheng Wang, Shung Haur Yang*

*此作品的通信作者

研究成果: Article同行評審

68 引文 斯高帕斯(Scopus)

摘要

Background and Objectives: In metastatic colorectal cancer, v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog (KRAS) is a predictive biomarker for anti-epidermal growth factor receptor (EGFR) treatment and V-raf murine sarcoma viral oncogene homolog B1 (BRAF) is a prognostic biomarker. We aimed to determine the impact of KRAS and BRAF mutation as determined from liver metastases specimens on overall survival (OS) in patients following colorectal liver metastasectomy. Methods: Liver metastases specimens (n = 292) obtained from patients after liver metastasectomy were used to determine the KRAS/BRAF genotype. Associations between clinicopathological parameters and KRAS/BRAF genotype were identified by univariate and multivariate analyses using the Cox proportional hazards model. The impact of KRAS/BRAF genotype on survival was analyzed using the Kaplan-Meier method. Results: The 5-year survival rate of the cohort was 55.8%. The KRAS and BRAF mutation rates were 38.0 and 2.1%, respectively. BRAF genotype, but not KRAS, was found to be an independent prognostic biomarker (HR = 5.181, P = 0.002) after adjustment for other significant confounding clinicopathological variates: Number of liver metastases (HR = 1.983, P = 0.009), concomitant extrahepatic disease (HR = 1.858, P = 0.014), and surgical margin (HR = 3.241, P < 0.001). BRAF genotype was an independent prognostic biomarker in patients with liver metastases only after metastasectomy (HR = 6.245, P < 0.003). Conclusions: BRAF mutation is an independent prognostic biomarker for colorectal liver metastasectomy.

原文English
頁(從 - 到)123-129
頁數7
期刊Journal of Surgical Oncology
106
發行號2
DOIs
出版狀態Published - 1 8月 2012

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