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卵巢癌的诊断生物标志物:超越CA125和HE4的进展。

Diagnostic biomarkers in ovarian cancer: advances beyond CA125 and HE4.

作者信息

Ghose Aruni, McCann Lucy, Makker Shania, Mukherjee Uma, Gullapalli Sri Vidya Niharika, Erekkath Jayaraj, Shih Stephanie, Mahajan Ishika, Sanchez Elisabet, Uccello Mario, Moschetta Michele, Adeleke Sola, Boussios Stergios

机构信息

Department of Medical Oncology, Barts Cancer Centre, St. Bartholomew's Hospital, Barts Health NHS Trust, London, UK.

Department of General Medicine, Newham University Hospital, Barts Health NHS Trust, London, UK.

出版信息

Ther Adv Med Oncol. 2024 Feb 29;16:17588359241233225. doi: 10.1177/17588359241233225. eCollection 2024.

Abstract

Ovarian cancer (OC) is the most lethal gynaecologic malignancy, attributed to its insidious growth, non-specific symptoms and late presentation. Unfortunately, current screening modalities are inadequate at detecting OC and many lack the appropriate specificity and sensitivity that is desired from a screening test. Nearly 70% of cases are diagnosed at stage III or IV with poor 5-year overall survival. Therefore, the development of a sensitive and specific biomarker for early diagnosis and screening for OC is of utmost importance. Currently, diagnosis is guided by CA125, the patient's menopausal status and imaging features on ultrasound scan. However, emerging evidence suggests that a combination of CA125 and HE4 (another serum biomarker) and patient characteristics in a multivariate index assay may provide a higher specificity and sensitivity than either CA125 and HE4 alone in the early detection of OC. Other attempts at combining various serum biomarkers into one multivariate index assay such as OVA1, ROMA and Overa have all shown promise. However, significant barriers exist before these biomarkers can be implemented in clinical practice. This article aims to provide an up-to-date review of potential biomarkers for screening and early diagnosis of OC which may have the potential to transform its diagnostic landscape.

摘要

卵巢癌(OC)是最致命的妇科恶性肿瘤,这归因于其隐匿性生长、非特异性症状以及就诊时已处于疾病晚期。不幸的是,目前的筛查方式在检测卵巢癌方面存在不足,许多方法缺乏筛查测试所期望的适当特异性和敏感性。近70%的病例在III期或IV期被诊断出来,5年总生存率较低。因此,开发一种用于卵巢癌早期诊断和筛查的敏感且特异的生物标志物至关重要。目前,诊断主要依据CA125、患者的绝经状态以及超声扫描的影像学特征。然而,新出现的证据表明,在多变量指标检测中,将CA125和HE4(另一种血清生物标志物)以及患者特征相结合,在卵巢癌的早期检测中可能比单独使用CA125或HE4具有更高的特异性和敏感性。将各种血清生物标志物组合成一个多变量指标检测的其他尝试,如OVA1、ROMA和Overa,都显示出了前景。然而,在这些生物标志物能够应用于临床实践之前,仍存在重大障碍。本文旨在对可能改变卵巢癌诊断格局的、用于卵巢癌筛查和早期诊断的潜在生物标志物进行最新综述。

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