Department of Ophthalmology, Ludwig-Maximilians-University, Munich, Germany.
Melanoma Res. 2011 Aug;21(4):352-6. doi: 10.1097/CMR.0b013e328347105e.
The serological marker melanoma inhibitory activity (MIA) has been shown to be significantly higher in the serum of patients suffering from metastatic uveal melanoma than in progression-free patients. The objective of this study was to calculate a meaningful receiver operating characteristic (ROC) curve for MIA based on a large patient collective and to find an appropriate threshold value. MIA tumor marker levels of 503 outpatients suffering from uveal melanoma were evaluated using enzyme-linked immunosorbent assay. Fifty-four patients had confirmed metastases and 449 patients showed no overt metastatic disease at the time the blood sample was taken. ROC analysis was performed and the area under the curve (AUC) was calculated. Metastatic patients showed significantly higher MIA levels (median 11.69 ng/ml) than patients in the group without overt metastatic disease (median 6.97 ng/ml) (the Mann-Whitney test, P<0.001). The AUC was 0.84 (95% confidence interval: 0.76-0.91). The ROC resulting from our study can be applied for test comparison by means of AUC. The AUC value of 0.84 for MIA demonstrates the accurate performance of the test. On the basis of this ROC curve, we propose a MIA threshold value for uveal melanoma patients of 8.3 ng/ml (with a corresponding sensitivity of 82% and specificity of 77%, positive predictive value of 0.30 and negative predictive value of 0.97). In patients with higher MIA serum levels, further diagnostics should be initiated.
血清标志物黑色素瘤抑制活性(MIA)在患有转移性葡萄膜黑色素瘤的患者血清中明显高于无进展患者。本研究的目的是基于大量患者群体计算 MIA 的有意义的接受者操作特征(ROC)曲线,并找到合适的阈值。采用酶联免疫吸附试验(ELISA)评估了 503 名患有葡萄膜黑色素瘤的门诊患者的 MIA 肿瘤标志物水平。54 名患者被证实有转移,449 名患者在采血时无明显转移性疾病。进行了 ROC 分析并计算了曲线下面积(AUC)。转移性患者的 MIA 水平明显高于无明显转移性疾病患者(中位数 11.69ng/ml)(Mann-Whitney 检验,P<0.001)。AUC 为 0.84(95%置信区间:0.76-0.91)。我们的研究得出的 ROC 可通过 AUC 用于测试比较。MIA 的 AUC 值为 0.84,表明该测试具有准确的性能。基于该 ROC 曲线,我们建议将 8.3ng/ml 作为葡萄膜黑色素瘤患者的 MIA 阈值(相应的敏感性为 82%,特异性为 77%,阳性预测值为 0.30,阴性预测值为 0.97)。对于 MIA 血清水平较高的患者,应启动进一步的诊断。