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A Protocol for Explant Cultures of IDH1-mutant Diffuse Low-grade Gliomas
Published on: May 9, 2025
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.
Background:
Update 3 of the Consortium to Inform Molecular and Practical Approaches to CNS Tumor Taxonomy (cIMPACT-NOW) recognizes amplification of epidermal growth factor receptor (EGFR) as one important aberration in diffuse gliomas (World Health Organization [WHO] grade II/III). While these recommendations endorse testing, a cost-effective, clinically relevant testing paradigm is currently lacking. Here, we use real-world clinical data to propose a financially effective diagnostic test algorithm in the context of new guidelines.
Methods:
To determine the prevalence, distribution, neuroradiographic features (Visually Accessible REMBRANDT Images [VASARI]), and prognostic relevance of EGFR amplification in lower-grade gliomas, we assembled a consecutive series of diffuse gliomas. For validation we included publicly available data from The Cancer Genome Atlas. For a cost-utility analysis we compared combined EGFR and isocitrate dehydrogenase (IDH) testing, EGFR testing based on IDH results, and no EGFR testing.
Results:
In n = 71 WHO grade II/III gliomas, we identified EGFR amplification in 28.2%. With one exception, all EGFR amplifications occurred in IDH-wildtype gliomas. Comparison of overall survival showed that EGFR amplification denotes a significantly more aggressive subset of tumors (P < 0.0001, log-rank). The radiologic phenotype in the EGFR-amplified tumors includes diffusion restriction (15%, P = 0.02), >5% tumor contrast enhancement (75%, P = 0.016), and mild (not avid) enhancement (P = 0.016). The proposed testing algorithm reserves EGFR fluorescence in situ hybridization (FISH) testing for IDH-wildtype cases. Implementation would result in ~37.9% cost reduction at our institution, or about $1.3-4 million nationally.
Conclusion:
EGFR-amplified diffuse gliomas are "glioblastoma-like" in their behavior and may represent undersampled glioblastomas, or subsets of IDH-wildtype diffuse gliomas with inherently aggressive biology. EGFR FISH after IDH testing is a financially effective and clinically relevant test algorithm for routine clinical practice.
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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