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Application of malignant pleural effusion cell blocks in the diagnosis and personalized treatment of advanced non-small cell lung carcinoma

机译:恶性胸腔积液在晚期非小细胞肺癌的诊断和个性化治疗中的应用

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Objective The aim of the study was to investigate the efficacy of immunocytochemistry and related gene detection using cell block for the diagnosis and individualized treatment of advanced lung cancer.Methods Sixty-five malignant pleural effusion specimens were collected to make cell blocks, which were used for hematoxylin and eosin(H&E) staining, immunocytochemical studies, and gene sequencing of the tumors to guide the individualized diagnoses and treatment of the given tumors. Results The tumor cells in the cell block sections were abundant in number with high quality cellular structures, and the histological morphological characteristics were partially maintained. Immunocytochemical staining was helpful in identifying the cell origin and tumor classification, and amplification refractory mutation system(ARMS) was used to determine the mutation status of epidermal growth factor receptor(EGFR). Of the 65 samples, 50 had a diagnosis of adenocarcinoma, 7 were pulmonary squamous cells, 6 were small cell carcinoma of the lung, and 2 were mesothelioma. The morphological features of the tumors were as follows: acinar formation, papillary and single cells for adenocarcinoma;intercellular bridges for squamous cell carcinoma;and morphology of the small cells is similar to that of the smear. Correlating with the results of immunocytochemical staining and clinical data analysis, 40 cases were confirmed as pulmonary adenocarcinoma, with an additional 4 cases of breast cancer, 3 cases of ovarian adenocarcinoma, and 3 cases of colorectal adenocarcinoma. Of the 47 non-small cell lung carcinoma(NSCLC) patients, EGFR mutations were detected in 26 cases(55.3%) by ARMS, with four mutation types: exon 19 deletion(13 cases, 50.0%), exon 2l point mutations L858R(11 cases, 42.3%) and L861Q(1 case, 3.8%), and exon 18 point mutation G719X(1 case, 3.8%). Conclusion Malignant pleural effusion cell blocks combined with immunocytochemical markers and molecular pathology are helpful for the diagnosis of advanced tumors, the identification of tumor properties and histological tumor origin, and the selection of individualized treatment for advanced lung cancer.
机译:目的研究细胞块免疫细胞化学和相关基因检测在晚期肺癌诊断和个体化治疗中的作用。方法收集65例恶性胸腔积液标本制作细胞块,用于肺癌的诊断。苏木和曙红(H&E)染色,免疫细胞化学研究以及肿瘤的基因测序,以指导对给定肿瘤的个性化诊断和治疗。结果细胞阻滞切片中的肿瘤细胞数量众多,细胞结构优质,部分保留了组织形态学特征。免疫细胞化学染色有助于鉴定细胞起源和肿瘤分类,并使用扩增难治性突变系统(ARMS)来确定表皮生长因子受体(EGFR)的突变状态。在65个样本中,有50个被诊断出患有腺癌,7个是肺鳞状细胞癌,6个是肺小细胞癌,2个是间皮瘤。肿瘤的形态学特征如下:腺癌的腺泡形成,乳头状和单细胞;鳞状细胞癌的细胞间桥;小细胞的形态与涂片相似。与免疫细胞化学染色结果和临床数据分析相关,确诊为肺腺癌40例,其中乳腺癌4例,卵巢腺癌3例,大肠腺癌3例。在47例非小细胞肺癌(NSCLC)患者中,ARMS检测到26例(55.3%)EGFR突变,有四种突变类型:外显子19缺失(13例,50.0%),外显子2l点突变L858R( 11例,42.3%)和L861Q(1例,3.8%),外显子18点突变G719X(1例,3.8%)。结论恶性胸腔积液结合免疫细胞化学标记物和分子病理学检查有助于晚期肿瘤的诊断,肿瘤性质的鉴定和组织学起源,以及对晚期肺癌个体化治疗的选择。

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