myeloMATCH is a National Cancer Institute (NCI) precision medicine clinical trial initiative to evaluate treatments for acute myeloid leukemia and myelodysplastic syndrome based on a leukemia's diagnostic molecular-genetic profile. The NCI myeloid assay version 2 (NMAv2) uses the Genexus System, an automated platform with <48-hour turnaround from specimen receipt to reporting, to provide harmonized regulatory-compliant use for myeloMATCH across two independent clinical laboratories. Using clinical specimens, cell lines, and contrived reference materials, NMAv2 exhibited 99% sensitivity for 291 known mutations and 100% specificity. High reproducibility detecting all reportable variants was observed, with >98% mean positive percentage agreement and 100% negative percent agreement across six reproducibility assessments. Reproducibility experiments of companion diagnostic biomarkers (1 to 1.5à clinical limit of reporting) showed 100% positive percentage agreement and negative percent agreement. The limit of detection was 0.06% for hotspot single-nucleotide variants, 0.16% for non-hotspot single-nucleotide variants, 0.51% for hotspot insertion/deletions, approximately 1% for non-hotspot insertion/deletions, 0.23% for FLT3-internal tandem duplications, and â¤40 reads at 0.1% tumor content for fusions. Concordance of 99.39% was observed in orthogonal assays testing 76 blinded myeloid specimens in the sensitivity study, and 100% concordance was observed in testing 54 FLT3-internal tandem duplication specimens. The results show that NMAv2 has high specificity, sensitivity, accuracy, and reproducibility, and can rapidly characterize genomic alterations in acute myeloid leukemia and myelodysplastic syndrome.
Analytical Performance of the NCI-myeloMATCH Assay: A Rapid Turnaround Genomic Profiling Assay for Myeloid Disorders.
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作者:Yeung Cecilia C S, Narava Srikrishna K, Chang Ting-Chia, Saeed Maria, Aicher Lauri, Beppu Lan W, Majano Marvin S, Taylor Erin M, Camalier Corinne E, Sandhuria Pooja, Sala-Torra Olga, Li Jessica, Yee Laura M, McShane Lisa M, Karlovich Chris, Little Richard F, Harris Lyndsay, Doroshow James H, Williams Paul M, Radich Jerald P, Jiwani Shahanawaz
| 期刊: | Journal of Molecular Diagnostics | 影响因子: | 3.400 |
| 时间: | 2025 | 起止号: | 2025 Aug;27(8):783-795 |
| doi: | 10.1016/j.jmoldx.2025.05.001 | ||
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