Back to Search Start Over

An independent validation of a gene expression signature to differentiate malignant melanoma from benign melanocytic nevi.

Authors :
Clarke LE
Flake DD 2nd
Busam K
Cockerell C
Helm K
McNiff J
Reed J
Tschen J
Kim J
Barnhill R
Elenitsas R
Prieto VG
Nelson J
Kimbrell H
Kolquist KA
Brown KL
Warf MB
Roa BB
Wenstrup RJ
Source :
Cancer [Cancer] 2017 Feb 15; Vol. 123 (4), pp. 617-628. Date of Electronic Publication: 2016 Oct 21.
Publication Year :
2017

Abstract

Background: 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.<br />Methods: 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.<br />Results: The gene expression signature differentiated benign nevi from malignant melanoma with a sensitivity of 91.5% and a specificity of 92.5%.<br />Conclusions: 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.<br /> (© 2016 Myriad Genetics, Inc. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society.)

Details

Language :
English
ISSN :
1097-0142
Volume :
123
Issue :
4
Database :
MEDLINE
Journal :
Cancer
Publication Type :
Academic Journal
Accession number :
27768230
Full Text :
https://doi.org/10.1002/cncr.30385