Frontiers in Oncology (Sep 2024)

ASPYRE-Lung: validation of a simple, fast, robust and novel method for multi-variant genomic analysis of actionable NSCLC variants in FFPE tissue

  • Ryan T. Evans,
  • Elizabeth Gillon-Zhang,
  • Julia N. Brown,
  • Katherine E. Knudsen,
  • Candace King,
  • Amanda S. Green,
  • Ana-Luisa Silva,
  • Justyna M. Mordaka,
  • Rebecca N. Palmer,
  • Alessandro Tomassini,
  • Alejandra Collazos,
  • Christina Xyrafaki,
  • Iyelola Turner,
  • Chau Ha Ho,
  • Dilyara Nugent,
  • Jinsy Jose,
  • Simonetta Andreazza,
  • Nicola D. Potts,
  • Kristine von Bargen,
  • Eleanor R. Gray,
  • Magdalena Stolarek-Januszkiewicz,
  • Aishling Cooke,
  • Honey V. Reddi,
  • Barnaby W. Balmforth,
  • Robert J. Osborne

DOI
https://doi.org/10.3389/fonc.2024.1420162
Journal volume & issue
Vol. 14

Abstract

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IntroductionGenomic variant testing of tumors is a critical gateway for patients to access the full potential of personalized oncology therapeutics. Current methods such as next-generation sequencing are costly and challenging to interpret, while PCR assays are limited in the number of variants they can cover. We developed ASPYRE® (Allele-Specific PYrophosphorolysis REaction) technology to address the urgent need for rapid, accessible and affordable diagnostics informing actionable genomic target variants of a given cancer. The targeted ASPYRE-Lung panel for non-small cell carcinoma covers 114 variants in 11 genes (ALK, BRAF, EGFR, ERBB2, KRAS, RET, ROS1, MET & NTRK1/2/3) to robustly inform clinical management. The assay detects single nucleotide variants, insertions, deletions, and gene fusions from tissue-derived DNA and RNA simultaneously.MethodsWe tested the limit of detection, specificity, analytical accuracy and analytical precision of ASPYRE-Lung using FFPE lung tissue samples from patients with non-small cell lung carcinoma, variant-negative FFPE tissue from healthy donors, and FFPE-based contrived samples with controllable variant allele fractions.ResultsThe sensitivity of ASPYRE-Lung was determined to be ≤ 3% variant allele fraction for single nucleotide variants and insertions or deletions, 100 copies for fusions, and 200 copies for MET exon 14 skipping. The specificity was 100% with no false positive results. The analytical accuracy test yielded no discordant calls between ASPYRE-Lung and expected results for clinical samples (via orthogonal testing) or contrived samples, and results were replicable across operators, reagent lots, runs, and real-time PCR instruments with a high degree of precision.ConclusionsThe technology is simple and fast, requiring only four reagent transfer steps using standard laboratory equipment (PCR and qPCR instruments) with analysis via a cloud-based algorithm. The ASPYRE-Lung assay has the potential to be transformative in facilitating access to rapid, actionable molecular profiling of tissue for patients with non-small cell carcinoma.

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