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具有分子和预后特征的侵袭性Ⅰ期肺腺癌亚型,类似于晚期肺癌。

An Aggressive Subtype of Stage I Lung Adenocarcinoma with Molecular and Prognostic Characteristics Typical of Advanced Lung Cancers.

机构信息

Molecular Medicine Program, European Institute of Oncology, Milan, Italy.

IFOM, The FIRC Institute for Molecular Oncology Foundation, Milan, Italy.

出版信息

Clin Cancer Res. 2017 Jan 1;23(1):62-72. doi: 10.1158/1078-0432.CCR-15-3005. Epub 2016 Jun 29.

Abstract

PURPOSE

The National Lung Cancer Screening Trial has confirmed that lung cancer mortality can be reduced if tumors are diagnosed early, that is, at stage I. However, a substantial fraction of stage I lung cancer patients still develop metastatic disease within 5 years from surgery. Prognostic biomarkers are therefore needed to identify patients at risk of an adverse outcome, who might benefit from multimodality treatment.

EXPERIMENTAL DESIGN

We extensively validated a 10-gene prognostic signature in a cohort of 507 lung adenocarcinoma patients using formalin-fixed paraffin-embedded samples. Furthermore, we performed an integrated analysis of gene expression, methylation, somatic mutations, copy number variations, and proteomic profiles on an independent cohort of 468 patients from The Cancer Genome Atlas (TCGA).

RESULTS

Stage I lung cancer patients (N = 351) identified as high-risk by the 10-gene signature displayed a 4-fold increased risk of death [HR = 3.98; 95% confidence interval (CI), 1.73-9.14], with a 3-year overall survival of 84.2% (95% CI, 78.7-89.7) compared with 95.6% (92.4-98.8) in low-risk patients. The analysis of TCGA cohort revealed that the 10-gene signature identifies a subgroup of stage I lung adenocarcinomas displaying distinct molecular characteristics and associated with aggressive behavior and poor outcome.

CONCLUSIONS

We validated a 10-gene prognostic signature capable of identifying a molecular subtype of stage I lung adenocarcinoma with characteristics remarkably similar to those of advanced lung cancer. We propose that our signature might aid the identification of stage I patients who would benefit from multimodality treatment. Clin Cancer Res; 23(1); 62-72. ©2016 AACR.

摘要

目的

国家肺癌筛查试验已经证实,如果肿瘤能够早期诊断,即处于 I 期,肺癌死亡率可降低。然而,相当一部分 I 期肺癌患者在手术后 5 年内仍会发展为转移性疾病。因此,需要有预后生物标志物来识别有不良预后风险的患者,这些患者可能受益于多模式治疗。

实验设计

我们使用福尔马林固定石蜡包埋样本,在 507 例肺腺癌患者的队列中广泛验证了一个 10 基因预后签名。此外,我们对来自癌症基因组图谱(TCGA)的 468 例独立患者队列的基因表达、甲基化、体细胞突变、拷贝数变异和蛋白质组谱进行了综合分析。

结果

通过 10 基因签名确定的 I 期肺癌患者(N=351)死亡风险增加了 4 倍[风险比(HR)=3.98;95%置信区间(CI),1.73-9.14],总生存率为 3 年 84.2%(95%CI,78.7-89.7),而低风险患者为 95.6%(92.4-98.8)。TCGA 队列的分析表明,该 10 基因签名确定了 I 期肺腺癌的一个分子亚群,其具有明显不同于晚期肺癌的分子特征,与侵袭性行为和不良预后相关。

结论

我们验证了一个 10 基因预后签名,该签名能够识别出具有与晚期肺癌非常相似特征的 I 期肺腺癌的分子亚型。我们提出,我们的签名可能有助于识别可能受益于多模式治疗的 I 期患者。临床癌症研究;23(1);62-72。©2016AACR。

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