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首页> 外文期刊>Journal of Clinical Oncology >Three-gene prognostic classifier for early-stage non small-cell lung cancer.
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Three-gene prognostic classifier for early-stage non small-cell lung cancer.

机译:早期非小细胞肺癌的三基因预后分类器。

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PURPOSE: Several microarray studies have reported gene expression signatures that classify non-small-cell lung carcinoma (NSCLC) patients into different prognostic groups. However, the prognostic gene lists reported to date overlap poorly across studies, and few have been validated independently using more quantitative assay methods. PATIENTS AND METHODS: The expression of 158 putative prognostic genes identified in previous microarray studies was analyzed by reverse transcription quantitative polymerase chain reaction in the tumors of 147 NSCLC patients. Concordance indices and risk scores were used to identify a stage-independent set of genes that could classify patients with significantly different prognoses. RESULTS: We have identified a three-gene classifier (STX1A, HIF1A, and CCR7) for overall survival (hazard ratio = 3.8; 95% CI, 1.7 to 8.2; P < .001). The classifier was also able to stratify stage I and II patients and further improved the predictive ability of clinical factors such as histology and tumor stage. The predictive value of this three-gene classifier was validated in two large independent microarray data sets from Harvard and Duke Universities. CONCLUSION: We have identified a new three-gene classifier that is independent of and improves on stage to stratify early-stage NSCLC patients with significantly different prognoses. This classifier may be tested further for its potential value to improve the selection of resected NSCLC patients in adjuvant therapy.
机译:目的:一些微阵列研究已经报道了将非小细胞肺癌(NSCLC)患者分为不同预后组的基因表达特征。然而,迄今为止报道的预后基因列表在各个研究中重叠性很差,并且很少使用更多的定量分析方法进行独立验证。病人和方法:通过逆转录定量聚合酶链反应分析了147例NSCLC患者肿瘤中158个推测的预后基因的表达。一致性指数和风险评分用于确定一组与阶段无关的基因,这些基因可以对预后明显不同的患者进行分类。结果:我们确定了总生存期的三基因分类器(STX1A,HIF1A和CCR7)(危险比= 3.8; 95%CI为1.7至8.2; P <.001)。该分类器还能够对I和II期患者进行分层,并进一步提高了临床因素如组织学和肿瘤分期的预测能力。在哈佛大学和杜克大学的两个大型独立微阵列数据集中验证了这种三基因分类器的预测价值。结论:我们已经确定了一种新的三基因分类器,该分类器独立于阶段并在阶段上有所改善,以对预后明显不同的早期NSCLC患者进行分层。可以进一步测试该分类器的潜在价值,以改善辅助治疗中切除的NSCLC患者的选择。

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