Literature DB >> 25960256

Analytical Performance of a 15-Gene Prognostic Assay for Early-Stage Non-Small-Cell Lung Carcinoma Using RNA-Stabilized Tissue.

Shuguang Huang1, Nicholas J Reitze1, Amy L Ewing1, Suzanne McCreary1, Arlette H Uihlein1, Stacey L Brower1, Dakun Wang1, Tianhua Wang1, Michael J Gabrin1, Katherine E Keating2, Jude Mulligan2, Claire Wilson2, Timothy Davison2, Stuart McKenzie2, Ming-Sound Tsao3, Frances A Shepherd3, Victoria Plamadeala4.   

Abstract

A 15-gene prognostic signature for early-stage, completely resected, non-small-cell lung carcinoma, (which distinguishes between patients with good and poor prognoses) was clinically validated in prior studies. To achieve operational efficiencies, this study was designed to evaluate the assay's performance in RNA-stabilized tissue as an alternative to the fresh-frozen tissue format originally used to develop the assay. The percent concordance between matched tissue formats was 84% (95% Wilson CI, 70%-92%), a level of agreement comparable to the inherent reproducibility of the assay observed within biological replicates of fresh-frozen tissue. Furthermore, the analytical performance of the assay using the RNA-stabilized tissue format was evaluated. When compared to an accredited reference laboratory, the clinical laboratory achieved a concordance of 94% (95% Wilson CI, 81%-98%), and there was no evidence of bias between the laboratories. The lower limit of quantitation for the target RNA concentration was confirmed to be, at most, 12.5 ng/μL. The assay reportable range defined in terms of risk score units was determined to be -4.295 to 4.210. In a large-scale precision study, the assay showed high reproducibility and repeatability. When subjected to a maximal amount of genomic DNA, a potential contaminant, the assay still produced the expected results. The 15-gene signature was confirmed to produce reliable results and, thus, is suitable for its intended use.
Copyright © 2015 American Society for Investigative Pathology and the Association for Molecular Pathology. Published by Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 25960256     DOI: 10.1016/j.jmoldx.2015.03.005

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN: 1525-1578            Impact factor:   5.568


  6 in total

1.  BORIS promotes chromatin regulatory interactions in treatment-resistant cancer cells.

Authors:  David N Debruyne; Ruben Dries; Satyaki Sengupta; Davide Seruggia; Yang Gao; Bandana Sharma; Hao Huang; Lisa Moreau; Michael McLane; Daniel S Day; Eugenio Marco; Ting Chen; Nathanael S Gray; Kwok-Kin Wong; Stuart H Orkin; Guo-Cheng Yuan; Richard A Young; Rani E George
Journal:  Nature       Date:  2019-08-07       Impact factor: 49.962

2.  Epithelial-to-Mesenchymal Transition Antagonizes Response to Targeted Therapies in Lung Cancer by Suppressing BIM.

Authors:  Kyung-A Song; Matthew J Niederst; Timothy L Lochmann; Aaron N Hata; Hidenori Kitai; Jungoh Ham; Konstantinos V Floros; Mark A Hicks; Haichuan Hu; Hillary E Mulvey; Yotam Drier; Daniel A R Heisey; Mark T Hughes; Neha U Patel; Elizabeth L Lockerman; Angel Garcia; Shawn Gillepsie; Hannah L Archibald; Maria Gomez-Caraballo; Tara J Nulton; Brad E Windle; Zofia Piotrowska; Sinem E Sahingur; Shirley M Taylor; Mikhail Dozmorov; Lecia V Sequist; Bradley Bernstein; Hiromichi Ebi; Jeffrey A Engelman; Anthony C Faber
Journal:  Clin Cancer Res       Date:  2017-10-19       Impact factor: 12.531

3.  A 16-gene expression signature to distinguish stage I from stage II lung squamous carcinoma.

Authors:  Rui Wang; Yuxing Cai; Baoping Zhang; Zhengxia Wu
Journal:  Int J Mol Med       Date:  2017-12-19       Impact factor: 4.101

4.  Reciprocal modulation of mesenchymal stem cells and tumor cells promotes lung cancer metastasis.

Authors:  Giulia Fregni; Mathieu Quinodoz; Emely Möller; Joanna Vuille; Sabine Galland; Carlo Fusco; Patricia Martin; Igor Letovanec; Paolo Provero; Carlo Rivolta; Nicolo Riggi; Ivan Stamenkovic
Journal:  EBioMedicine       Date:  2018-02-23       Impact factor: 8.143

5.  Epigenetic Inactivation of the Tumor Suppressor IRX1 Occurs Frequently in Lung Adenocarcinoma and Its Silencing Is Associated with Impaired Prognosis.

Authors:  Miriam M Küster; Marc A Schneider; Antje M Richter; Sarah Richtmann; Hauke Winter; Mark Kriegsmann; Soni S Pullamsetti; Thorsten Stiewe; Rajkumar Savai; Thomas Muley; Reinhard H Dammann
Journal:  Cancers (Basel)       Date:  2020-11-26       Impact factor: 6.639

6.  Predicting Prognosis of Early-Stage Non-Small Cell Lung Cancer Using the GeneFx® Lung Signature.

Authors:  Sandy Der; Chang-Qi Zhu; Stacey Brower; Arlette Uihlein
Journal:  PLoS Curr       Date:  2015-10-26
  6 in total

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