喉癌中的自身抗体:检测和作为生物标记物的作用。

Thashani Gunasekera, Umapriyatharshini Rajagopalan, Samith Herath, Sameera Samarakoon, Rizny Sakkaff, Roshan Jalaldeen
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引用次数: 0

摘要

目的:之前尚未专门研究过自身抗体(AAb)作为血清学生物标志物在喉癌(LC)中的诊断作用。本研究调查了抗喉癌 AAb 的存在及其作为喉癌早期诊断生物标志物的潜力,以改善患者的预后:方法:采用间接酶联免疫吸附试验(ELISA)检测 LC 患者(30 人)和健康人(30 人)的抗 LC AAb 水平。分析了患者 AAb 水平与各种临床因素(主要是肿瘤分期)的关系:结果:LC 患者的 AAb 水平明显高于对照组(P = .019)。AAb水平检测对LC检测的敏感性、特异性、阳性预测值(PPV)、阴性预测值(NPV)和准确性均为70%。阳性似然比(LR+)和阴性似然比(LR-)分别为 2.33 和 0.43。AAb水平与癌症分期(P = .708)、首次出现症状后的持续时间(P = .228)、就医时间(P = .231)和风险因素暴露程度(P = .478)无关:结论:在诊断结果良好的 LC 患者中,无论处于哪个阶段,都能检测到显著水平的 AAbs。因此,抗 LC AAbs 有可能被用作 LC 早期诊断的预测性生物标记物。
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Autoantibodies in laryngeal cancer: detection and role as a biomarker.

Objective: Diagnostic role of autoantibodies (AAb) as serological biomarkers has not been specifically investigated in laryngeal cancer (LC) previously. The study investigates the presence of anti-LC AAbs and their potential as a biomarker for early diagnosis of LC, to improve patient outcome.

Method: Anti-LC AAb levels were investigated in LC patients (n = 30) and healthy individuals (n = 30) by indirect enzyme-linked immunosorbent assay (ELISA). Patient AAb levels were analyzed with various clinical factors, primarily tumor stage.

Results: AAb levels were significantly higher in LC patients than in the control group (P = .019). The diagnostic performance of AAb-level testing for LC detection presented a sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), and accuracy of 70% each. The positive likelihood (LR+) and negative likelihood (LR-) ratios were 2.33 and 0.43, respectively. AAb levels were independent of cancer stage (P = .708), duration since first appearance of symptoms (P = .228), duration of medical attention (P = .231), and degree of risk-factor exposure (P = .478).

Conclusion: Significant level of AAbs could be detected among LC patients with good diagnostic performance, irrespective of stage. Thus, anti-LC AAbs reflect potential to be utilized as predictive biomarkers in early diagnostics of LC.

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