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Application of Ventana immunocytochemical analysis on ThinPrep cytology slides for detection of ALK rearrangement in patients with advanced non–small-cell lung cancer

机译:Ventana免疫细胞化学分析对薄雾细胞学载玻片的应用,用于检测晚期非小细胞肺癌患者ALK重排

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摘要

Abstract Background Ventana ALK (D5F3) screening of anaplastic lymphoma kinase (ALK) gene rearrangement in tissue specimens has been approved by US FDA (Food and Drug Administration) to select treatment for non–small-cell lung carcinoma (NSCLC). However, tumor tissues are often not readily obtainable, and cytology specimens and may be the only tumor material available for diagnosis and molecular marker analysis. In this study, we evaluated the feasibility of ALK immunocytochemistry (ICC) on ThinPrep slides and determined a suitable scoring system for interpretation of the results. Methods One hundred twenty-one fine-needle aspirate (FNA) specimens from metastatic lesions of NSCLC were analyzed. ALK rearrangement was detected on ThinPrep cytology slides using the Ventana immunocytochemistry ALK-D5F3 system, which adopts two scoring systems for interpretation of the ICC results. The results were subsequently confirmed by reverse transcription polymerase chain reaction (RT-PCR) analysis and fluorescence in situ hybridization (FISH). Results Among the 121 ICC specimens, 16 that were considered ALK-positive by either scoring system were referred for PCR analysis. Among the ALK ICC-negative cases, 33 had correlated FISH ALK results. A total of 49 specimens that exhibited either a positive or negative ICC result with a correlated ALK status were analyzed statistically. ICC results showed a high concordance rate with the results of PCR/FISH analysis. The sensitivity and specificity of ALK ICC by the binary scoring algorithm were 68.75 and 96.97%, respectively. These values increased to 93.75 and 96.97%, respectively, when interpreted by the semiquantified interpretation system. Conclusions ALK ICC analysis on ThinPrep slides is a reliable ALK testing method, and the semiquantified interpretation system on cytology specimens is recommended rather than the binary scoring algorithm on tissue specimens.
机译:摘要背景Ventana Alk(D5F3)筛选组织标本中的包血性淋巴瘤激酶(ALK)基因重新排列已被美国FDA(食品和药物管理局)批准为非小细胞肺癌(NSCLC)的治疗。然而,肿瘤组织通常不容易获得,并且细胞学标本,并且可以是可用于诊断和分子标记分析的唯一肿瘤材料。在这项研究中,我们评估了Alk免疫细胞化学(ICC)对薄雾载玻片的可行性,并确定了用于解释结果的合适评分系统。方法分析了来自NSCLC转移性病变的一百二十一颗细针吸气(FNA)标本。在使用Ventana免疫细胞化学ALK-D5F3系统上检测到薄雾细胞学载玻片上检测到ALK重排,这采用两种评分系统来解释ICC结果。随后通过逆转录聚合酶链反应(RT-PCR)分析和原位杂交(鱼)的荧光证实结果。结果在121个ICC标本中,参考PCR分析的评分系统被认为是Alk阳性的16个。在ALK ICC阴性病例中,33例具有相关的鱼ALK结果。在统计上分析了总共49种,表现出具有相关ALK状态的阳性或阴性ICC结果。 ICC结果显示了PCR /鱼分析结果的高度一致率。 BAL ICC通过二进制评分算法的敏感性和特异性分别为68.75和96.97%。当由半装饰解释系统解释时,这些值分别增加到93.75和96.97%。结论薄雾载玻片上的ALK ICC分析是一种可靠的ALK测试方法,建议使用细胞学标本的半缀化解释系统而不是组织标本的二元评分算法。

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