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首页> 外文期刊>Thoracic cancer. >Tumor MET expression profile predicts the outcome of non‐small cell lung cancer patients receiving epidermal growth factor receptor tyrosine kinase inhibitors
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Tumor MET expression profile predicts the outcome of non‐small cell lung cancer patients receiving epidermal growth factor receptor tyrosine kinase inhibitors

机译:肿瘤MET表达谱可预测接受表皮生长因子受体酪氨酸激酶抑制剂的非小细胞肺癌患者的预后

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AbstractBackgroundThis study assesses whether MET expression in tumor tissue is associated with an increased sensitivity to epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitors (TKIs) in non-small-cell lung cancer (NSCLC) patients.MethodsThis retrospective study included 69 NSCLC participants with available tumor tissue and data on treatment response and survival. MET and hepatocyte growth factor expression in tumor tissue were evaluated by immunohistochemistry.ResultsPositive tMET expression correlated with a shorter progression-free survival (PFS; P = 0.003) and overall survival (OS; P = 0.05). Positive pY1234/1235 expression was significantly associated with a longer PFS (P = 0.031) and OS (P = 0.012). In multivariable analyses, tMET and pY1234/1235 expression were independent factors for PFS and OS, respectively. (tMET, PFS; P = 0.02, OS; P = 0.0007 and pY1234/1234, PFS; P = 0.01, OS; P = 0.004).ConclusionsThis study suggests that total and phosphorylated MET expression in tumor tissue is potentially useful for the selection of NSCLC patients who are likely to benefit from EGFR-TKIs, irrespective of their EGFR status.
机译:摘要背景:这项研究评估了非小细胞肺癌(NSCLC)患者对肿瘤组织中MET表达是否与对表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKIs)的敏感性增加有关的方法。提供可用的肿瘤组织以及有关治疗反应和生存率的数据。用免疫组织化学方法评估肿瘤组织中的MET和肝细胞生长因子表达。结果tMET阳性表达与较短的无进展生存期(PFS; P = 0.003)和总生存期(OS; P = 0.05)相关。 pY1234 / 1235阳性表达与更长的PFS(P = 0.031)和OS(P = 0.012)显着相关。在多变量分析中,tMET和pY1234 / 1235的表达分别是PFS和OS的独立因素。 (tMET,PFS; P = 0.02,OS; P = 0.0007和pY1234 / 1234,PFS; P = 0.01,OS; P = 0.004)结论本研究表明肿瘤组织中总的和磷酸化的MET表达可能对选择有用可能受益于EGFR-TKI的NSCLC患者中,无论其EGFR状态如何。

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