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2015年世界卫生组织分类下肺大细胞癌的临床病理及遗传学特征:一项初步研究

Clinicopathological and genetic characteristics of pulmonary large cell carcinoma under 2015 WHO classification: a pilot study.

作者信息

Liu Renwang, Liu Jinghao, Shi Tao, Li Xiongfei, Ren Dian, Chen Gang, Li Ying, Liu Hongyu, Xu Song, Chen Jun

机构信息

Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China.

Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Lung Cancer Institute, Tianjin Medical University General Hospital, Tianjin 300052, China.

出版信息

Oncotarget. 2017 Oct 11;8(59):100754-100763. doi: 10.18632/oncotarget.21736. eCollection 2017 Nov 21.

Abstract

Pulmonary large cell carcinoma (LCC) was re-defined under the 2015 WHO classification criteria. However, the clinicopathological features and genetic mutation statuses of Chinese LCC patients based on the new classification have rarely been investigated. Twenty-four Chinese surgically resected LCC patients previously diagnosed under the 2004 WHO criteria were re-classified under the 2015 WHO criteria. Genetic analysis was performed using next-generation sequencing of 46 cancer-related genes. The correlation of clinicopathological and genetic data was further analyzed. Eight patients were re-defined as LCCs, and 16 patients were defined as non-LCCs under the refined criteria. All LCC patients were male, and 7 patients were smokers. No significant differences in age, gender, smoking status, primary site, TNM staging and overall survival were observed between the LCC and non-LCC patients under the refined criteria. Four of the 8 LCC patients presented TP53 mutations, and no somatic mutations were detected in the other 4 LCCs under the refined criteria. For the 16 non-LCCs, not only TP53 and KRAS but also EGFR, KIT, PIK3CA, PTEN, IDH1, APC, ATM and BRAF mutations were also observed. In addition, LCCs without TP53 mutations did not present any gene mutations under the 2004 or 2015 WHO criteria. Importantly, the patients with TP53 mutation exhibited a trend with a worse survival outcome at the time of follow-up. The new WHO diagnosis criteria have superior performance in precise molecular classification for LCC patients.

摘要

肺大细胞癌(LCC)在2015年世界卫生组织(WHO)分类标准下被重新定义。然而,基于新分类的中国LCC患者的临床病理特征和基因突变状态鲜有研究。对24例先前根据2004年WHO标准诊断的中国手术切除的LCC患者,按照2015年WHO标准重新分类。使用46个癌症相关基因的二代测序进行基因分析。进一步分析临床病理和基因数据的相关性。按照细化标准,8例患者被重新定义为LCC,16例患者被定义为非LCC。所有LCC患者均为男性,7例患者吸烟。在细化标准下,LCC和非LCC患者在年龄、性别、吸烟状态、原发部位、TNM分期和总生存期方面未观察到显著差异。8例LCC患者中有4例出现TP53突变,按照细化标准,其他4例LCC未检测到体细胞突变。对于16例非LCC,不仅观察到TP53和KRAS突变,还观察到EGFR、KIT、PIK3CA、PTEN、IDH1、APC、ATM和BRAF突变。此外,在2004年或2015年WHO标准下,无TP53突变的LCC未出现任何基因突变。重要的是,TP53突变患者在随访时显示出生存结局较差的趋势。新的WHO诊断标准在LCC患者的精确分子分类方面具有卓越性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ed93/5725061/3dcf42688628/oncotarget-08-100754-g001.jpg

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