Suppr超能文献

[采用2015年世界卫生组织标准对肺活检进行诊断及检测相关致癌驱动基因突变]

[Diagnosis of lung biopsy employing the 2015 WHO criteria and detection of related oncogenic driver mutations].

作者信息

Fang F, Qiao X B, Yang L, Di J, Hu S T, Liu D G, Lyu N

机构信息

Department of Pathology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China; Department of Pathology, Beijing Hospital, National Center of Gerontology, Beijing 100730, China.

Department of Pathology, Beijing United Family Hospital, Beijing 100015, China.

出版信息

Zhonghua Bing Li Xue Za Zhi. 2019 Apr 8;48(4):270-275. doi: 10.3760/cma.j.issn.0529-5807.2019.04.002.

Abstract

The diagnostic criteria of lung biopsy specimens by 2015 WHO lung tumor classification were used to evaluate lung biopsy specimens along with detection of genetic alterations of major tumor driving genes including epidermal growth factor receptor (EGFR). The clinical data, histological slides, immunohistochemical stains and special stains of 806 lung biopsy specimens at Beijing Hospital from July 2015 to July 2018 were retrospectively analyzed. Diagnosis of lung cancer was reclassified according to the 2015 WHO lung tumor classification and related gene mutation data were analyzed. During a three-year period, the total number of lung cancer diagnosis was 483 cases, including 221 female and 262 male patients with age ranging from 37 to 85 years (median age of 65 years). There were 40 cases(8.28%) of small cell carcinoma,11 cases (2.28%) of large cell neuroendocrine carcinoma, 3 cases (0.62%) of combined neuroendocrine carcinoma, 2 cases(0.41%) of atypical carcinoid, 208 cases (43.06%) of adenocarcinoma, 92 cases(19.05%) of non-small cell carcinoma, favor adenocarcinoma, 66 cases (13.66%) of squamous cell carcinoma, 42 cases(8.70%) of non-small cell carcinoma, favor squamous cell carcinoma, 16 cases(3.31%) of non-small cell carcinoma, not otherwise specified, and 3 cases (0.62%) of non-small cell carcinoma, possible adenosquamous carcinoma. Among 202 cases tested, 107 cases (52.97%) showed EGFR mutations, including 86 of 133 cases (64.66%) of adenocarcinoma and 18 of 52 cases (34.62%) of non-small cell carcinoma, favor adenocarcinoma. Twenty two cases were found to have T790M mutation among 27 patients after EGFR TKI targeted drug therapy. Immunohistochemical staining of ALK (D5F3) was positive in 3 of 354 cases of non-small cell lung cancer, confirmed by EML4-ALK fusion gene fluorescence PCR. ROS1 gene fusion was found in 1 of 38 cases. Splicing mutations in exon 14 of MET gene were seen in one case of non-small cell carcinoma with spindle cell differentiation. The new diagnostic criteria by the 2015 WHO lung tumor classification is better suited for diagnosing lung biopsy specimens and providing accurate treatment guidance and improving the patient outcome.

摘要

采用2015年世界卫生组织(WHO)肺肿瘤分类的肺活检标本诊断标准,对肺活检标本进行评估,并检测包括表皮生长因子受体(EGFR)在内的主要肿瘤驱动基因的基因改变。回顾性分析了2015年7月至2018年7月北京医院806例肺活检标本的临床资料、组织学切片、免疫组化染色及特殊染色。根据2015年WHO肺肿瘤分类对肺癌诊断进行重新分类,并分析相关基因突变数据。在三年期间,肺癌诊断总数为483例,其中女性221例,男性262例,年龄范围为37至85岁(中位年龄65岁)。小细胞癌40例(8.28%),大细胞神经内分泌癌11例(2.28%),混合性神经内分泌癌3例(0.62%),非典型类癌2例(0.41%),腺癌208例(43.06%),非小细胞癌,倾向腺癌92例(19.05%),鳞状细胞癌66例(13.66%),非小细胞癌,倾向鳞状细胞癌42例(8.70%),非小细胞癌,未另行特指16例(3.31%),非小细胞癌,可能为腺鳞癌3例(0.62%)。在检测的202例中,107例(52.97%)显示EGFR突变,其中腺癌133例中的86例(64.66%),非小细胞癌,倾向腺癌52例中的18例(34.62%)。EGFR TKI靶向药物治疗后,27例患者中有22例检测到T790M突变。354例非小细胞肺癌中,3例ALK(D5F3)免疫组化染色阳性,经EML4-ALK融合基因荧光PCR证实;38例中有1例检测到ROS1基因融合;1例具有梭形细胞分化的非小细胞癌中发现MET基因外显子14的剪接突变。2015年WHO肺肿瘤分类的新诊断标准更适合于诊断肺活检标本,为治疗提供准确指导并改善患者预后。

相似文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验