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A specific KRAS codon 13 mutation is an independent predictor for colorectal cancer metachronous distant metastases

机译:特定的KRAS密码子13突变是大肠癌异时远处转移的独立预测因子

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Background: In colorectal cancer, there are significant differences between synchronous and metachronous distant metastases. However in recent studies, synchronous and metachronous metastases were always lumped together, neglecting their clinical and molecular differences. The mechanism of the latency of metachronous metastases is still unclear. We conducted this study to reveal the relationship between EGFR pathways and metachronous metastases, and try to find efficient predictors. Methods: PCRs and pyrosequencing were used to detect KRAS, BRAF, PIK3CA and PTEN mutations in primary tumor tissues in a total of 281 patients from 2002 to 2008. Patients were identified into three groups: no-metastases group, synchronous-metastases group and metachronous-metastases group. Clinical and survival data were collected from a prospective database. Results: KRAS codon 13 mutation was an independent predictor only for metachronous distant metastases (OR = 11.857, P < 0.001), but not for synchronous metastases. Male gender (OR = 2.233, P = 0.024), primary tumor located at rectum (OR = 0.404, P = 0.041), and primary pN2 stage (OR = 3.361, P = 0.01) were also independent predictors for metachronous distant metastases. Different SNPs in KRAS worked significantly different in determining synchronous or metachronous metastases. BRAF mutation (Univariate, OR = 11.5, P = 0.039) and > 200 ng/ml preoperative CEA (Univariate, OR = 41, P = 0.011) potentially predicted metastases within 6 months after primary tumor resection. After metachronous metastases, radical resection (HR = 0.280, P = 0.002) was the most important protective factor for long-term survival. Conclusion: There were significant clinical and molecular differences between synchronous and metachronous metastases. As an independent predictor, KRAS codon 13 mutation might be the key to explain the mechanism of colorectal cancer metachronous distant metastases. Together with clinical characteristics, it could aid in the early detection of metachronous metastases.
机译:背景:在大肠癌中,同步和异时远处转移之间存在显着差异。但是,在最近的研究中,同步转移和异时转移总是被混在一起,而忽略了它们的临床和分子差异。异时转移潜伏期的机制仍不清楚。我们进行了这项研究以揭示EGFR途径与异时转移之间的关系,并试图找到有效的预测因子。方法:采用PCR和焦磷酸测序技术检测2002年至2008年共281例原发肿瘤组织中的KRAS,BRAF,PIK3CA和PTEN突变。将患者分为三组:无转移组,同步转移组和异时组。 -转移组。从前瞻性数据库中收集临床和生存数据。结果:KRAS 13位密码子突变仅是远处远处转移的独立预测因子(OR = 11.857,P <0.001),但不是同步转移。男性(OR = 2.233,P = 0.024),原发于直肠的肿瘤(OR = 0.404,P = 0.041)和原发性pN2分期(OR = 3.361,P = 0.01)也是异位远处转移的独立预测因子。在确定同步或异时转移时,KRAS中不同的SNP的工作方式明显不同。 BRAF突变(单因素,OR = 11.5,P = 0.039)和术前CEA> 200 ng / ml(单因素,OR = 41,P = 0.011)可能在原发肿瘤切除后6个月内预测转移。转移后,根治性切除(HR = 0.280,P = 0.002)是长期生存的最重要保护因素。结论:同步转移和异时转移之间存在明显的临床和分子差异。作为独立的预测因子,KRAS 13号密码子突变可能是解释大肠癌异时远处转移机制的关键。结合临床特征,它可以帮助早期发现异时转移。

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