Creaney Jenette, Robinson Bruce W S
National Centre for Asbestos Related Diseases, Western Australian Institute of Medical Research, University of Western Australia, 4th Floor, G block, Sir Charles Gairdner Hospital, Verdun St, Nedlands, WA 6009, Australia.
Curr Opin Pulm Med. 2009 Jul;15(4):366-70. doi: 10.1097/MCP.0b013e32832b98eb.
Malignant mesothelioma is an asbestos-induced, aggressive tumour. In centres across the world, research has focused on evaluating biomarkers for malignant mesothelioma screening, diagnosis, prognostication and monitoring. With the incidence of malignant mesothelioma expected to increase, it is timely to review the current status of biomarkers in this field.
The majority of recent studies have evaluated the commercial MESOMARK assay in a diagnostic setting. Studies have clarified that soluble-shed mesothelin as well as mesothelin-related peptide are targets of the assay. The assay sensitivity ranges from 50% at diagnosis to 84% in advanced disease. The assay has a high level of specificity relative to benign lung and pleural conditions and is positive in 10-15% of other malignancies. In a prospective screen of 538 asbestos-exposed workers, 2.8% were positive; one had lung cancer that was subsequently successfully treated. The biomarkers megakaryocyte potentiating factor, osteopontin and CA125, either alone or in combination with soluble mesothelin, have also been assessed.
To date, soluble mesothelin remains the best available biomarker for malignant mesothelioma. However, a lack of sensitivity for early-stage disease and for all malignant mesothelioma histologies provides motivation for the search of novel malignant mesothelioma biomarkers with greater sensitivity, especially for very early disease.
恶性间皮瘤是一种由石棉诱发的侵袭性肿瘤。在世界各地的研究中心,研究重点一直是评估用于恶性间皮瘤筛查、诊断、预后评估和监测的生物标志物。鉴于恶性间皮瘤的发病率预计将会上升,适时回顾该领域生物标志物的当前状况很有必要。
近期的大多数研究在诊断环境中评估了商业化的MESOMARK检测法。研究已明确可溶性脱落间皮素以及间皮素相关肽是该检测法的靶点。该检测法的敏感性在诊断时为50%,在晚期疾病中为84%。相对于良性肺部和胸膜疾病,该检测法具有较高的特异性,在10% - 15%的其他恶性肿瘤中呈阳性。在对538名接触石棉工人的前瞻性筛查中,2.8%呈阳性;其中一人患有肺癌,随后成功接受了治疗。巨核细胞增强因子、骨桥蛋白和CA125等生物标志物也已单独或与可溶性间皮素联合进行了评估。
迄今为止,可溶性间皮素仍然是恶性间皮瘤现有的最佳生物标志物。然而,对早期疾病以及所有恶性间皮瘤组织学类型缺乏敏感性,促使人们寻找具有更高敏感性的新型恶性间皮瘤生物标志物,尤其是针对极早期疾病。