Duffy M J, van Dalen A, Haglund C, Hansson L, Holinski-Feder E, Klapdor R, Lamerz R, Peltomaki P, Sturgeon C, Topolcan O
Department of Pathology and Laboratory Medicine, Nuclear Medicine Laboratory, St Vincent's University Hospital, Elm Park, Dublin 4, Ireland.
Eur J Cancer. 2007 Jun;43(9):1348-60. doi: 10.1016/j.ejca.2007.03.021. Epub 2007 May 18.
The aim of this article is to present updated guidelines for the use of serum, tissue and faecal markers in colorectal cancer (CRC). Lack of specificity and sensitivity preclude the use of all existing serum markers for the early detection of CRC. For patients with stage II or stage III CRC who may be candidates for either liver resection or systemic treatment should recurrence develop, CEA should be measured every 2-3 months for at least 3 years after diagnosis. Insufficient evidence exists to recommend routine use of tissue factors such as thymidylate synthase, microsatellite instability (MSI), p53, K-ras and deleted in colon cancer (DCC) for either determining prognosis or predicting response to therapy in patients with CRC. Microsatellite instability, however, may be used as a pre-screen for patients with suspected hereditary non-polyposis colorectal cancer. Faecal occult blood testing but not faecal DNA markers may be used to screen asymptomatic subjects 50 years or older for early CRC.
本文旨在介绍结直肠癌(CRC)血清、组织和粪便标志物使用的最新指南。缺乏特异性和敏感性使得所有现有的血清标志物都无法用于CRC的早期检测。对于可能在复发时适合进行肝切除或全身治疗的II期或III期CRC患者,诊断后至少3年内应每2 - 3个月测量一次癌胚抗原(CEA)。目前尚无足够证据推荐常规使用组织因子,如胸苷酸合成酶、微卫星不稳定性(MSI)、p53、K-ras和结肠癌缺失(DCC)来确定CRC患者的预后或预测其对治疗的反应。然而,微卫星不稳定性可作为疑似遗传性非息肉病性结直肠癌患者的预筛查指标。粪便潜血试验而非粪便DNA标志物可用于筛查50岁及以上无症状受试者的早期CRC。