Analytical validity of DecisionDx-SCC, a gene expression profile test to identify risk of metastasis in cutaneous squamous cell carcinoma (SCC) patients

被引:8
|
作者
Borman, Sherri [1 ]
Wilkinson, Jeff [1 ]
Meldi-Sholl, Lauren [1 ]
Johnson, Clare [1 ]
Carter, Kelsey [1 ]
Covington, Kyle R. [2 ]
Fitzgerald, Alison L. [2 ]
Kurley, Sarah J. [2 ]
Farberg, Aaron S. [3 ]
Goldberg, Matthew S. [2 ,4 ]
Monzon, Federico A. [2 ]
Oelschlager, Kristen [1 ]
Cook, Robert W. [2 ]
机构
[1] Castle Biosci Inc, Phoenix, AZ USA
[2] Castle Biosci Inc, 505 S Friendswood Dr,Ste 400, Friendswood, TX 77546 USA
[3] Baylor Scott & White Hlth Syst, Dallas, TX USA
[4] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
关键词
Gene expression profiling; DecisionDx-SCC; Cutaneous squamous cell carcinoma; Metastasis; Analytic validity;
D O I
10.1186/s13000-022-01211-w
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background To improve identification of patients with cutaneous squamous cell carcinoma (SCC) at high risk for metastatic disease, the DecisionDx-SCC assay, a prognostic 40-gene expression profile (40-GEP) test, was developed and validated. The 40-GEP assay utilizes RT-PCR gene expression analysis on primary tumor biopsy tissue to evaluate the expression of 34 signature gene targets and 6 normalization genes. The test provides classifications of low risk (Class 1), moderate risk (Class 2A), and high risk (Class 2B) of metastasis within 3 years of diagnosis. The primary objective of this study was to validate the analytical performance of the 40-gene expression signature. Methods The repeatability and reproducibility of the 40-GEP test was evaluated by performance of inter-assay, intra-assay, and inter-operator precision experiments along with monitoring the reliability of sample and reagent stability for class call concordance. The technical performance of clinical orders from September 2020 through July 2021 for the 40-GEP test was assessed. Results Patient hematoxylin and eosin (H&E) stained slides were reviewed by a board-certified pathologist to assess minimum acceptable tumor content. Class specific controls (Class 1 and Class 2B) were evaluated with Levey-Jennings analysis and demonstrated consistent and reproducible results. Inter-assay, inter-operator and intra-assay concordance were all >= 90%, with short-term and long-term RNA stability also meeting minimum concordance requirements. Of the 2586 orders received, 93.5% remained eligible for testing, with 97.1% of all tested samples demonstrating actionable class call results. Conclusion DecisionDx-SCC demonstrates a high degree of analytical precision, yielding high concordance rates across multiple performance experiments, along with exhibiting robust technical reliability on clinical samples.
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页数:9
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