German Cancer Research Center, Heidelberg, Germany.
Am J Gastroenterol. 2010 Mar;105(3):682-90. doi: 10.1038/ajg.2009.668. Epub 2009 Dec 1.
Quantitative and qualitative immunochemical fecal occult blood tests (FOBTs) have been proposed for noninvasive colorectal cancer screening, but comparative evaluation is lacking. The aim of this study was to determine the diagnostic accuracy of two (quantitative) enzyme-linked immunosorbent assay (ELISA)-based immunochemical FOBTs for identifying colorectal adenomas in the target population of screening and to compare the results with six (qualitative) immunochromatographic FOBTs, previously evaluated in the same study participants using the same stool samples.
A total of 1,319 participants of screening colonoscopy at average risk for colorectal neoplasia (mean age 63 years; age range 31-86 years; 50% men) were recruited prospectively from January 2006 to December 2007 in collaboration with 20 gastroenterological practices in Germany. Fecal hemoglobin and hemoglobin-haptoglobin levels were measured using an automated ELISA (RIDASCREEN). Test performance characteristics at different cutoff values were derived by comparing the results of stool testing with the results of colonoscopy in a blinded manner.
A total of 130 participants (10%) had an advanced adenoma. The area under the receiver-operating characteristic curve with regard to advanced adenomas was 0.68 (0.65-0.71) for hemoglobin and 0.64 (0.61-0.67) for hemoglobin-haptoglobin (P=0.034). At a specificity of approximately 95%, the sensitivity (95% confidence interval) for advanced adenomas was 33% (25-42%) for hemoglobin and 24% (17-32%) for hemoglobin-haptoglobin, respectively. The sensitivity for hemoglobin was very close to sensitivities of the six qualitative FOBTs at (strongly divergent) levels of specificity observed for the latter.
ELISA-based measurement of hemoglobin was superior to hemoglobin-haptoglobin, but showed a similar sensitivity for advanced adenomas compared with (qualitative) immunochromatographic FOBTs at defined levels of specificity. Compared with the latter, its quantitative nature offers advantages in terms of transparency and flexibility regarding the positivity threshold (e.g., specificity can be oriented toward available colonoscopy resources or personal risk profiles) and in terms of a higher level of standardization regarding test analysis and interpretation.
定量和定性免疫化学粪便潜血检测(FOBT)已被提议用于非侵入性结直肠癌筛查,但缺乏比较评估。本研究的目的是确定两种(定量)酶联免疫吸附试验(ELISA)基于免疫化学 FOBT 在筛查目标人群中识别结直肠腺瘤的诊断准确性,并将结果与之前在同一研究参与者中使用相同粪便样本评估的六种(定性)免疫层析 FOBT 进行比较。
2006 年 1 月至 2007 年 12 月,与德国 20 家胃肠病学实践合作,前瞻性招募了 1319 名平均结直肠肿瘤风险筛查结肠镜检查参与者(平均年龄 63 岁;年龄范围 31-86 岁;50%为男性)。使用自动化 ELISA(RIDASCREEN)测量粪便血红蛋白和血红蛋白-触珠蛋白水平。通过盲法比较粪便检测结果与结肠镜检查结果,得出不同临界值下的测试性能特征。
共有 130 名参与者(10%)患有高级腺瘤。血红蛋白和血红蛋白-触珠蛋白对高级腺瘤的受试者工作特征曲线下面积分别为 0.68(0.65-0.71)和 0.64(0.61-0.67)(P=0.034)。在特异性约为 95%的情况下,高级腺瘤的敏感性(95%置信区间)分别为血红蛋白 33%(25-42%)和血红蛋白-触珠蛋白 24%(17-32%)。血红蛋白的敏感性非常接近后者在观察到的特异性(强烈不同)水平上的六种定性 FOBT 的敏感性。
基于 ELISA 的血红蛋白测量优于血红蛋白-触珠蛋白,但与(定性)免疫层析 FOBT 相比,在定义的特异性水平上对高级腺瘤具有相似的敏感性。与后者相比,其定量性质在阳性阈值方面具有透明度和灵活性(例如,可以针对可用的结肠镜检查资源或个人风险概况进行特异性定位),并且在测试分析和解释方面具有更高的标准化水平。