Diagnostic Pathology (May 2024)

Evaluation of the rapid Idylla IDH1-2 mutation assay in FFPE glioma samples

  • James P. Solomon,
  • Carlos Munoz-Zuluaga,
  • Cheyanne Slocum,
  • Alicia Dillard,
  • Lin Cong,
  • Jiajing Wang,
  • Neal Lindeman,
  • Michael Kluk,
  • Benjamin Liechty,
  • David Pisapia,
  • Hanna Rennert,
  • Priya D. Velu

DOI
https://doi.org/10.1186/s13000-024-01492-3
Journal volume & issue
Vol. 19, no. 1
pp. 1 – 9

Abstract

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Abstract IDH1 and IDH2 mutational status is a critical biomarker with diagnostic, prognostic, and treatment implications in glioma. Although IDH1 p.R132H-specific immunohistochemistry is available, it is unable to identify other mutations in IDH1/2. Next-generation sequencing can accurately determine IDH1/2 mutational status but suffers from long turnaround time when urgent treatment planning and initiation is medically necessary. The Idylla assay can detect IDH1/2 mutational status from unstained formalin-fixed paraffin-embedded (FFPE) slides in as little as a few hours. In a clinical validation, we demonstrate clinical accuracy of 97% compared to next-generation sequencing. Sensitivity studies demonstrated a limit of detection of 2.5-5% variant allele frequency, even at DNA inputs below the manufacturer’s recommended threshold. Overall, the assay is an effective and accurate method for rapid determination of IDH1/2 mutational status.

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