K-RAS基因突变的存在不影响结直肠癌肺转移灶切除术后的生存。

ISRN surgery Pub Date : 2014-02-04 eCollection Date: 2014-01-01 DOI:10.1155/2014/157586
Jon Zabaleta, Borja Aguinagalde, José M Izquierdo, Nerea Bazterargui, Stephany M Laguna, Maialen Martin-Arruti, Carmen Lobo, José I Emparanza
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引用次数: 7

摘要

介绍。我们的目的是确定K-RAS基因在结直肠癌(CRC)肺转移病例中的突变,并确定它们的存在是否是生存的预后因素。方法。我们纳入了1998年至2010年间手术的所有结直肠癌肺转移患者。通过DNA直接测序研究K-RAS突变。通过Kaplan-Meier法对数秩检验和多变量Cox回归分析探讨生存率差异。结果:90例患者共行110次手术干预。与生存率显著相关的因素有无病间隔(P = 0.002)、年龄(P = 0.007)、转移瘤数量(P = 0.001)、淋巴结累及(P = 0.007)、转移瘤大小(P = 0.013)和既往肝转移(P = 0.003)。在79例患者中,30例发现K-RAS突变。我们没有发现原生K-RAS和突变K-RAS的生存率有统计学差异(P = 0.913)。我们发现K-RAS突变患者的肺部复发率更高(P = 0.040),复发时间更短(P = 0.015)。Gly12Asp突变与高复发率(P = 0.022)和低生存率(P = 0.389)相关。结论。K-RAS突变在肺转移中的存在不影响总体生存,但与较高的肺复发率相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Presence of Mutations in the K-RAS Gene Does Not Affect Survival after Resection of Pulmonary Metastases from Colorectal Cancer.

The Presence of Mutations in the K-RAS Gene Does Not Affect Survival after Resection of Pulmonary Metastases from Colorectal Cancer.

Introduction. Our objective was to identify mutations in the K-RAS gene in cases of pulmonary metastases from colorectal cancer (CRC) and determine whether their presence was a prognostic factor for survival. Methods. We included all patients with pulmonary metastases from CRC operated on between 1998 and 2010. K-RAS mutations were investigated by direct sequencing of DNA. Differences in survival were explored with the Kaplan-Meier method log-rank tests and multivariate Cox regression analysis. Results. 110 surgical interventions were performed on 90 patients. Factors significantly associated with survival were disease-free interval (P = 0.002), age (P = 0.007), number of metastases (P = 0.001), lymph node involvement (P = 0.007), size of the metastases (P = 0.013), and previous liver metastasis (P = 0.003). Searching in 79 patients, K-RAS mutations were found in 30 cases. We did not find statistically significant differences in survival (P = 0.913) comparing native and mutated K-RAS. We found a higher rate of lung recurrence (P = 0.040) and shorter time to recurrence (P = 0.015) in patients with K-RAS mutations. Gly12Asp mutation was associated with higher recurrence (P = 0.022) and lower survival (P = 0.389). Conclusions. The presence of K-RAS mutations in pulmonary metastases does not affect overall survival but is associated with higher rates of pulmonary recurrence.

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