肿瘤标志物在与原发性肺腺癌相关的恶性胸腔积液中的流行:一项回顾性研究。

IF 1.8 Q3 RESPIRATORY SYSTEM
European Clinical Respiratory Journal Pub Date : 2021-10-31 eCollection Date: 2021-01-01 DOI:10.1080/20018525.2021.1984375
Katrine Fjaellegaard, Jesper Koefod Petersen, Gitte Andersen, Matteo Biagini, Rahul Bhatnagar, Christian B Laursen, Paul Frost Clementsen, Uffe Bodtger
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引用次数: 0

摘要

背景:原发性肺腺癌(AC)的肿瘤治疗包括靶向程序性死亡配体1 (PD-L1)、表皮生长因子受体(EGFR)突变和间变性淋巴瘤激酶(ALK)通路的药物。该研究的目的是报道这些肿瘤标志物在肺AC细胞学阳性的胸膜液中的流行程度,以及胸膜液容量测试的潜在影响。方法:我们回顾性地回顾了两年来在丹麦西兰大学医院呼吸内科介入科室进行的所有胸腔手术。ALK和PD-L1检测采用免疫组织化学,EGFR检测采用下一代测序。我们纳入了含有来自原发性肺AC的恶性细胞的胸膜液标本,并至少有一种临床医生要求的肿瘤标志物。结果:927例胸腔积液标本中,符合入选标准的有57例。PD-L1、ALK和EGFR分别为35/55(64%)、38/57(67%)和26/47(55%)。当分析容量> 50 mL时,患病率没有增加(p = 0.21-0.58)。结论:在含有肺AC细胞的胸膜液标本中,肿瘤标志物可在半数以上的病例中被证实。因此,与胸腔穿刺相比,补充侵入性手术有可能等待这些分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The prevalence of tumour markers in malignant pleural effusions associated with primary pulmonary adenocarcinoma: a retrospective study.

The prevalence of tumour markers in malignant pleural effusions associated with primary pulmonary adenocarcinoma: a retrospective study.

The prevalence of tumour markers in malignant pleural effusions associated with primary pulmonary adenocarcinoma: a retrospective study.

Background: Oncological treatment of primary pulmonary adenocarcinoma (AC) includes drugs targeting the pathways involving programmed death-ligand 1 (PD-L1), epidermal growth factor receptor (EGFR) mutation and anaplastic lymphoma kinase (ALK). The aim of the study was to report the prevalence of these tumour markers in pleural fluid with cytology positive for pulmonary AC and the potential influence of volume pleural fluid tested.

Methods: We retrospectively reviewed all thoracenteses performed in a two-year period at our interventional unit at Department of Respiratory Medicine at Zealand University Hospital Naestved, Denmark. ALK and PD-L1 testing was done using immunohistochemistry and EGFR testing using next-generation sequencing. We included pleural fluid specimens containing malignant cells originating from primary pulmonary AC and with at least one tumour marker requested by the clinicians.

Results: When screening 927 pleural fluid specimens, we identified 57 in accordance with the inclusion criteria. PD-L1, ALK and EGFR were obtained in 35/55 (64%), 38/57 (67%) and 26/47 (55%), respectively. The prevalence did not increase when analysing volumes > 50 mL (p = 0.21-0.58).

Conclusion: Tumour markers in pleural fluid specimens containing cells from pulmonary AC can be demonstrated in more than half of the cases. Therefore, supplementary invasive procedures than thoracentesis could potentially await these analyses.

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CiteScore
3.80
自引率
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15
审稿时长
16 weeks
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