Bast Robert C
Trans Am Clin Climatol Assoc. 2004;115:233-47; discussion 247-8.
Elimination of cancer in the 21st Century is likely to depend not only on more effective individualized treatment, but also upon earlier detection and prevention of different malignancies. Screening strategies for ovarian cancer have centered on the serum tumor marker CA 125, transvaginal sonography (TVS), or sequential use of the two modalities. A single determination of CA 125 is neither sufficiently sensitive nor specific to be used as an initial stage in screening. Specificity can be improved by monitoring CA 125 over time with an algorithm that estimates risk of ovarian cancer. Sensitivity of CA125 can be improved by use of multiple markers in combination. Gene expression array analysis, proteomics and lipomics are being utilized to identify markers that can be used in combination with CA 125 to detect >95% of early stage ovarian cancers. To maintain high specificity, values for different markers are being combined using novel approaches of neural network analysis and mixed multivariate analysis. Sequential use of multiple markers and TVS could provide a cost-effective strategy to detect a disease of intermediate prevalence.
21世纪癌症的消除可能不仅取决于更有效的个体化治疗,还取决于不同恶性肿瘤的早期检测和预防。卵巢癌的筛查策略主要集中在血清肿瘤标志物CA 125、经阴道超声检查(TVS)或两种方法的序贯使用。单次测定CA 125作为筛查的初始阶段既不够敏感也不够特异。通过使用一种估计卵巢癌风险的算法随时间监测CA 125,可以提高特异性。联合使用多种标志物可以提高CA125的敏感性。基因表达阵列分析、蛋白质组学和脂质组学正被用于识别可与CA 125联合使用以检测>95%早期卵巢癌的标志物。为了保持高特异性,正在使用神经网络分析和混合多变量分析的新方法来组合不同标志物的值。序贯使用多种标志物和TVS可以提供一种经济有效的策略来检测中等患病率的疾病。