Financially effective test algorithm to identify an aggressive, EGFR-amplified variant of IDH-wildtype, lower-grade

Tejus A Bale1,2, Justin T Jordan1,3,4, Otto Rapalino5

  • 1Department of Pathology, Massachusetts General Hospital, Boston, Massachusetts.

Neuro-Oncology
|November 30, 2018
PubMed
Abstract

Insights

Epidermal growth factor receptor (EGFR) amplification is common in diffuse gliomas. A new testing algorithm, performing EGFR fluorescence in situ hybridization (FISH) after isocitrate dehydrogenase (IDH) testing, is cost-effective and clinically relevant.

Area of Science:

  • Neuro-oncology
  • Molecular diagnostics
  • Cancer genomics

Background:

  • Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy (cIMPACT-NOW) Update 3 identifies epidermal growth factor receptor (EGFR) amplification as a key aberration in World Health Organization (WHO) grade II/III diffuse gliomas.
  • Current guidelines recommend EGFR testing, but a cost-effective and clinically applicable testing paradigm is lacking.

Purpose of the Study:

  • To determine the prevalence, distribution, neuroradiographic features, and prognostic significance of EGFR amplification in lower-grade gliomas.
  • To propose a cost-effective diagnostic testing algorithm for EGFR amplification in diffuse gliomas.

Main Methods:

  • Retrospective analysis of 71 WHO grade II/III diffuse gliomas with real-world clinical data.
  • Validation using The Cancer Genome Atlas (TCGA) data.
  • Cost-utility analysis comparing different EGFR testing strategies (combined EGFR/isocitrate dehydrogenase [IDH] testing, EGFR testing based on IDH results, no EGFR testing).

Main Results:

  • EGFR amplification was identified in 28.2% of diffuse gliomas, predominantly in IDH-wildtype cases.
  • EGFR amplification was associated with significantly shorter overall survival (P < 0.0001), indicating a more aggressive tumor subset.
  • Radiographic features of EGFR-amplified tumors included diffusion restriction, significant contrast enhancement, and mild enhancement patterns.
  • The proposed algorithm, reserving EGFR fluorescence in situ hybridization (FISH) for IDH-wildtype gliomas, demonstrated a potential cost reduction of ~37.9%.

Conclusions:

  • EGFR-amplified diffuse gliomas exhibit aggressive, "glioblastoma-like" behavior.
  • These tumors may represent an aggressive subset of IDH-wildtype diffuse gliomas or undersampled glioblastomas.
  • EGFR FISH testing subsequent to IDH testing provides a financially effective and clinically relevant diagnostic algorithm for routine practice.

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