KRAS and BRAF mutations are prognostic biomarkers in patients undergoing lung metastasectomy of colorectal cancer

被引:69
作者
Renaud, S. [1 ,2 ]
Romain, B. [2 ,3 ]
Falcoz, P-E [1 ]
Olland, A. [1 ]
Santelmo, N. [1 ]
Brigand, C. [3 ]
Rohr, S. [3 ]
Guenot, D. [2 ]
Massard, G. [1 ]
机构
[1] Strasbourg Univ Hosp, Nouvel Hop Civil, Dept Thorac Surg, F-67000 Strasbourg, France
[2] Strasbourg Univ, F-67000 Strasbourg, France
[3] Strasbourg Univ Hosp, Hop Hautepierre, Dept Gen & Digest Surg, F-67000 Strasbourg, France
关键词
BRAF; KRAS; lung; metastases; colorectal cancer; KIRSTEN RAS MUTATIONS; K-RAS; PULMONARY RESECTION; LIVER METASTASES; V600E MUTATION; CARCINOMA; SURVIVAL; IMPACT; TRIAL; EGFR;
D O I
10.1038/bjc.2014.499
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We evaluated KRAS (mKRAS (mutant KRAS)) and BRAF (mBRAF (mutant BRAF)) mutations to determine their prognostic potential in assessing patients with colorectal cancer (CRC) for lung metastasectomy. Methods: Data were reviewed from 180 patients with a diagnosis of CRC who underwent a lung metastasectomy between January 1998 and December 2011. Results: Molecular analysis revealed mKRAS in 93 patients (51.7%), mBRAF in 19 patients (10.6%). In univariate analyses, overall survival (OS) was influenced by thoracic nodal status (median OS: 98 months for pN-, 27 months for pN+, P < 0.0001), multiple thoracic metastases (75 months vs 101 months, P = 0.008) or a history of liver metastases (94 months vs 101 months, P = 0.04). mBRAF had a significantly worse OS than mKRAS and wild type (WT) (P < 0.0001). The 5-year OS was 0% for mBRAF, 44% for mKRAS and 100% for WT, with corresponding median OS of 15, 55 and 98 months, respectively (P < 0.0001). In multivariate analysis, WT BRAF (HR: 0.005 (95% CI: 0.001-0.02), P < 0.0001) and WT KRAS (HR: 0.04 (95% CI: 0.02-0.1), P < 0.0001) had a significant impact on OS. Conclusions: mKRAS and mBRAF seem to be prognostic factors in patients with CRC who undergo lung metastasectomy. Further studies are necessary.
引用
收藏
页码:720 / 728
页数:9
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