细胞角蛋白片段19.1和19.21 (Cyfra 21-1)在鉴别恶性和良性胸腔积液中的应用

Y C Lee, B S Knox, J E Garrett
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引用次数: 26

摘要

背景:恶性和良性胸腔积液的鉴别通常是困难的。血清Cyfra 21-1水平是细胞角蛋白19片段的标志物,已被用于上皮肿瘤的诊断和监测,特别是支气管源性癌。目的:本研究旨在建立积液Cyfra 21-1水平在鉴别恶性与良性积液中的作用。方法:将48例经细胞学或胸膜活检证实的恶性积液与34例良性标本进行比较。Cyfra 21-1浓度采用固相夹心放射免疫分析法(Centocur, USA)测定。结果:Cyfra 21-1水平在恶性积液中(几何平均值123.6 ng/mL, 95%可信区间[CI] 76.6-199.4)明显高于良性积液(几何平均值14.3 ng/mL, 95%可信区间[CI] 8.5-23.9)。结论:Cyfra 21-1在积液检查中是一种有用的辅助手段,但不应取代常规检查,因为良性组和恶性组之间的水平有相当大的重叠。它不能区分恶性肿瘤的亚群。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Use of cytokeratin fragments 19.1 and 19.21 (Cyfra 21-1) in the differentiation of malignant and benign pleural effusions.

Background: Differentiation between malignant and benign pleural effusions is often difficult. Serum level of Cyfra 21-1, a marker of cytokeratin 19 fragments, has been used in the diagnosis and monitoring of epithelial tumours, especially bronchogenic carcinomas.

Aim: This study is designed to establish the usefulness of effusion Cyfra 21-1 level in differentiating malignant from benign effusions.

Methods: Forty-eight malignant effusion aspirates (proven by cytology or pleural biopsy) and 34 benign samples were compared. Cyfra 21-1 concentration was measured by a solid phase sandwich radioimmunoassay (Centocur, USA).

Results: Cyfra 21-1 level was significantly higher in malignant effusions (geometric mean 123.6 ng/mL, 95% confidence interval [CI] 76.6-199.4) than in benign ones (geometric mean 14.3 ng/mL, 95% CI 8.5-23.9), p<0.00005. By Receiver Operating Characteristics curve analysis, the sensitivity is 77% for a specificity of 79% if the cut-off is set at 32 ng/mL. No significant difference was observed (p=0.1) in Cyfra 21-1 concentration between adenocarcinoma and mesothelioma effusions. Cyfra 21-1 level was not influenced by the effusion protein concentration (r=0.29), or by renal function as measured by serum creatinine (r=0.1). There was no significant difference between Cyfra 21-1 levels in benign exudate and transudate effusions, p=0.28.

Conclusions: Cyfra 21-1 is a useful adjunct in the workup of effusions but should not replace conventional investigations as there is considerable overlap in levels between benign and malignant groups. It is unable to differentiate between subgroups of malignancies.

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