Clarke Loren E, Flake Darl D, Busam Klaus, Cockerell Clay, Helm Klaus, McNiff Jennifer, Reed Jon, Tschen Jaime, Kim Jinah, Barnhill Raymond, Elenitsas Rosalie, Prieto Victor G, Nelson Jonathan, Kimbrell Hillary, Kolquist Kathryn A, Brown Krystal L, Warf M Bryan, Roa Benjamin B, Wenstrup Richard J
Myriad Genetic Laboratories, Inc, Salt Lake City, Utah.
Myriad Genetics, Inc, Salt Lake City, Utah.
Cancer. 2017 Feb 15;123(4):617-628. doi: 10.1002/cncr.30385. Epub 2016 Oct 21.
Recently, a 23-gene signature was developed to produce a melanoma diagnostic score capable of differentiating malignant and benign melanocytic lesions. The primary objective of this study was to independently assess the ability of the gene signature to differentiate melanoma from benign nevi in clinically relevant lesions.
A set of 1400 melanocytic lesions was selected from samples prospectively submitted for gene expression testing at a clinical laboratory. Each sample was tested and subjected to an independent histopathologic evaluation by 3 experienced dermatopathologists. A primary diagnosis (benign or malignant) was assigned to each sample, and diagnostic concordance among the 3 dermatopathologists was required for inclusion in analyses. The sensitivity and specificity of the score in differentiating benign and malignant melanocytic lesions were calculated to assess the association between the score and the pathologic diagnosis.
The gene expression signature differentiated benign nevi from malignant melanoma with a sensitivity of 91.5% and a specificity of 92.5%.
These results reflect the performance of the gene signature in a diverse array of samples encountered in routine clinical practice. Cancer 2017;123:617-628. © 2016 American Cancer Society.
最近,一种23基因特征被开发出来,用于生成一种黑色素瘤诊断评分,该评分能够区分恶性和良性黑素细胞病变。本研究的主要目的是独立评估该基因特征在临床相关病变中区分黑色素瘤与良性痣的能力。
从临床实验室前瞻性提交进行基因表达检测的样本中选取一组1400个黑素细胞病变。每个样本都经过检测,并由3名经验丰富的皮肤病理学家进行独立的组织病理学评估。为每个样本指定一个初步诊断(良性或恶性),并且纳入分析的样本需要3名皮肤病理学家之间的诊断一致性。计算该评分在区分良性和恶性黑素细胞病变中的敏感性和特异性,以评估该评分与病理诊断之间的关联。
该基因表达特征区分良性痣与恶性黑色素瘤的敏感性为91.5%,特异性为92.5%。
这些结果反映了该基因特征在常规临床实践中遇到的各种样本中的表现。《癌症》2017年;123:617 - 628。©2016美国癌症协会。