Department of Internal Medicine, UT Southwestern Medical Center, Dallas, Texas; Harold C. Simmons Cancer Center, UT Southwestern Medical Center, Dallas, Texas.
Department of Data Science, Dana Farber Cancer Center, Boston, Massachusetts.
Clin Gastroenterol Hepatol. 2022 Apr;20(4):953-955.e2. doi: 10.1016/j.cgh.2021.04.018. Epub 2021 Apr 20.
Hepatocellular carcinoma (HCC) surveillance is associated with early tumor detection and improved survival in patients with cirrhosis. Surveillance is performed using semiannual abdominal ultrasound with or without α-fetoprotein (AFP); however, this strategy misses more than one-third of HCC at an early stage. These data highlight a need for novel surveillance strategies with higher accuracy for early HCC detection. GALAD and Doylestown Plus are novel biomarker panels that combine multiple biomarkers with patient demographic and clinical characteristics; both demonstrated promising accuracy in phase II case-control studies; however, case-control studies can overestimate biomarker performance, highlighting a need for phase III cohort and nested case-control studies. Our study aimed to compare multiple biomarkers (including AFP, GALAD, and Doylestown Plus) in a nested case-control study of patients with cirrhosis.
肝细胞癌 (HCC) 监测与肝硬化患者的早期肿瘤检测和生存改善相关。监测采用半年一次的腹部超声联合或不联合甲胎蛋白 (AFP) 进行;然而,这种策略会错过三分之一以上的早期 HCC。这些数据突出表明需要新的监测策略,以提高早期 HCC 的检测准确性。GALAD 和 Doylestown Plus 是新的生物标志物组合,将多个生物标志物与患者的人口统计学和临床特征相结合;这两种方法在 II 期病例对照研究中均显示出有前景的准确性;然而,病例对照研究可能会高估生物标志物的性能,因此需要进行 III 期队列和嵌套病例对照研究。我们的研究旨在比较多个生物标志物(包括 AFP、GALAD 和 Doylestown Plus)在肝硬化患者的嵌套病例对照研究中的表现。