首页> 美国卫生研究院文献>International Journal of Otolaryngology >Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes
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Prevalence of K-RAS Codons 12 and 13 Mutations in Locally Advanced Head and Neck Squamous Cell Carcinoma and Impact on Clinical Outcomes

机译:局部晚期头颈部鳞状细胞癌中K-RAS密码子12和13突变的患病率及其对临床结果的影响

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摘要

Background. RAS gene mutations have an impact on treatment response and overall prognosis for certain types of cancer. Objectives. To determine the prevalence and impact of K-RAS codons 12 and 13 mutations in patients with locally advanced HNSCC treated with primary or adjuvant chemo-radiation. Methods. 428 consecutive patients were treated with chemo-radiation therapy and followed for a median of 37 months. From these, 199 paraffin embedded biopsy or surgical specimens were retrieved. DNA was isolated and analyzed for K-RAS mutational status. Results. DNA extraction was successful in 197 samples. Of the 197 specimens, 3.5% presented K-RAS codon 12 mutations. For mutated cases and non-mutated cases, complete initial response to chemoradiation therapy was 71 and 73% (P = 0.32). LRC was respectively 32 and 83% (P = 0.03), DFS was 27 and 68% (P = 0.12), distant metastasis-free survival was 100 and 81% (P = 0.30) and OS was 57 and 65% (P = 0.14) at three years. K-Ras codon 13 analysis revealed no mutation. Conclusion. K-RAS codon 12 mutational status, although not associated with a difference in response rate, may influence the failure pattern and the type of therapy offered to patients with HNSCC. Our study did not reveal any mutation of K-RAS codon 13.
机译:背景。 RAS基因突变会影响某些类型癌症的治疗反应和总体预后。目标。若要确定患K-RAS密码子12和13突变在原发性或辅助性化学放射治疗的局部晚期HNSCC患者中的发生率和影响。方法。连续428例患者接受了化学放射治疗,中位时间为37个月。从这些样本中,检索出199个石蜡包埋的活检或手术标本。分离DNA并分析K-RAS突变状态。结果。 DNA提取成功于197个样品。在197个样本中,有3.5%呈现K-RAS密码子12突变。对于突变病例和非突变病例,对化学放射治疗的完全初始反应分别为71%和73%(P = 0.32)。 LRC分别为32%和83%(P = 0.03),DFS为27%和68%(P = 0.12),无远处无转移生存率分别为100%和81%(P = 0.30)和OS为57%和65%(P = 0.14)在三年。 K-Ras密码子13分析显示没有突变。结论。 K-RAS密码子12突变状态尽管与应答率的差异无关,但可能会影响失败模式和为HNSCC患者提供的治疗类型。我们的研究未发现K-RAS密码子13的任何突变。

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