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近期 PD-L1 表达定量研究进展:CT 引导下细针穿刺活检中放射科医生的观点。

Recent advancement on PD-L1 expression quantification: the radiologist perspective on CT-guided FNAC.

机构信息

Radiology Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

Lung Disease Unit, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.

出版信息

Diagn Interv Radiol. 2021 Mar;27(2):214-218. doi: 10.5152/dir.2021.19545.

Abstract

PURPOSE

We aimed to evaluate the feasibility, accuracy, and safety of Programmed Death-1/ Programmed Death-Ligand 1 (PD-1/ PD-L1) expression quantification in cytology cell-block samples obtained through transthoracic CT-guided fine-needle aspiration cytology (FNAC) from the interventional radiologist's perspective.

METHODS

We performed a consecutive unselected series of 361 CT-guided biopsies of pulmonary nodules and masses which came to our observation from June 2017 to October 2018. For each case, exhaustive clinical, morphologic, molecular and tomographic data were available. All the material obtained was fixed in formalin to obtain a cell-block for the pathologist, who performed immunohistochemical analysis to detect PD-L1 expression levels on each sample.

RESULTS

Of all the analyzed samples, 93.6% (338/361) were defined to be diagnostic, including neoplastic (72%, 260/361) and non-neoplastic lesions (21.6%, 78/361); only 6.4% (23/361) of them resulted in nondiagnostic specimens. Non-small cell lung cancer (NSCLC) accounted for 73.8% of neoplastic lesions (192/260): most of them were adenocarcinoma (83%, 160/192), followed by squamous carcinoma (14%, 27/192) and poorly differentiated carcinoma (3%, 5/192). In 96% of NSCLC (184/192), the diagnosis was reached either in the absence of complications or with early minor complications. PD-L1 expression was evaluated in all 192 NSCLC cytology specimens: 180 immunostainings were found to be adequate for PD-L1 testing. In 76% of cases, PD-L1 expression level was lower than 50%.

CONCLUSION

The findings of our study indicate that PD-L1 quantification using a cell-block approach on CT-guided FNAC is a feasible and safe technique and should be taken into account alongside with core biopsy approach, especially in case of advanced disease and/or fragile and older patients.

摘要

目的

我们旨在评估从介入放射学家的角度来看,通过经胸 CT 引导下细针抽吸细胞学(FNAC)获得的细胞学细胞块样本中程序性死亡受体 1/程序性死亡配体 1(PD-1/PD-L1)表达定量的可行性、准确性和安全性。

方法

我们对 2017 年 6 月至 2018 年 10 月期间来我院观察的 361 例肺结节和肿块的 CT 引导下活检进行了连续的、未选择的系列研究。对每例患者,都可获得详尽的临床、形态学、分子和影像学数据。所有获得的材料均用福尔马林固定,以便病理学家获得细胞块,并对每个样本进行免疫组织化学分析以检测 PD-L1 表达水平。

结果

在所有分析的样本中,93.6%(338/361)被定义为诊断性的,包括肿瘤性(72%,260/361)和非肿瘤性病变(21.6%,78/361);只有 6.4%(23/361)的样本结果为非诊断性标本。非小细胞肺癌(NSCLC)占肿瘤性病变的 73.8%(192/260):其中大多数为腺癌(83%,160/192),其次为鳞状细胞癌(14%,27/192)和低分化癌(3%,5/192)。在 96%(184/192)的 NSCLC 中,诊断结果是在没有并发症或仅有早期轻微并发症的情况下获得的。对所有 192 例 NSCLC 细胞学标本进行了 PD-L1 表达评估:180 例免疫染色被认为足以进行 PD-L1 检测。在 76%的病例中,PD-L1 表达水平低于 50%。

结论

我们的研究结果表明,使用 CT 引导下 FNAC 的细胞块方法进行 PD-L1 定量是一种可行且安全的技术,应与核心活检方法一起考虑,尤其是在晚期疾病和/或脆弱和老年患者中。

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