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BIOMARKER:

IDH mutation + NTRK fusion

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Other names: IDH2, Isocitrate Dehydrogenase (NADP(+)) 2, Isocitrate Dehydrogenase (NADP(+)) 2, Mitochondrial, Isocitrate Dehydrogenase 2 (NADP+), Mitochondrial, Isocitrate Dehydrogenase [NADP], Mitochondrial, Oxalosuccinate Decarboxylase, NADP(+)-Specific ICDH, ICD-M, IDH, IDP, MNADP-IDH, D2HGA2, IDHM, IDPM; HEL-216, HEL-S-26, Epididymis Luminal Protein 216, Isocitrate Dehydrogenase 1 (NADP+), Epididymis Secretory Protein Li 26, IDH1, Isocitrate Dehydrogenase (NADP(+)) 1, Isocitrate Dehydrogenase 1 (NADP+), Soluble; NTRK | Neurotrophic receptor tyrosine kinase | High Affinity Nerve Growth Factor Receptor | Neurotrophic Tyrosine Kinase, Receptor| TRK1-Transforming Tyrosine Kinase Protein | Tropomyosin-Related Kinase A | Tyrosine Kinase Receptor A | P140-TrkA | Gp140trk | TRKA | Trk-A | Neurotrophic Tyrosine Kinase Receptor
Entrez ID:
Associations
Trials
2ms
Molecular Testing in Gliomas: What is Necessary in Routine Clinical Practice? (PubMed, Curr Oncol Rep)
MGMT promoter methylation testing is the most established molecular marker for response to temozolomide in IDH wild-type glioblastoma and in turn impacts overall survival. Moreover, identification of certain mutations and molecular markers, such as BRAF V600E, hypermutation or elevated tumor-mutational burden and NTRK fusions allow for the use of FDA approved agents that are tumor-agnostic. Finally, molecular testing opens options for clinical trials that are essential for diseases with limited treatment options like gliomas.
Review • Journal • Tumor mutational burden
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BRAF (B-raf proto-oncogene) • TMB (Tumor Mutational Burden) • MGMT (6-O-methylguanine-DNA methyltransferase) • NTRK (Neurotrophic receptor tyrosine kinase)
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BRAF V600E • BRAF V600 • MGMT promoter methylation • IDH wild-type • IDH mutation + BRAF V600E • IDH mutation + NTRK fusion • NTRK fusion
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temozolomide
2ms
All-in-one bimodal DNA and RNA next-generation sequencing panel for integrative diagnosis of glioma. (PubMed, Pathol Res Pract)
Overall, our results suggest that the all-in-one bimodal DNA/RNA panel is reliable for detecting diagnostic gene alterations in accordance with the latest WHO classification. The integrative pathological and molecular strategy could be valuable in confirmation of diagnosis and selection of treatment options for brain tumors.
Journal • Next-generation sequencing
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EGFR (Epidermal growth factor receptor) • FGFR3 (Fibroblast growth factor receptor 3) • NTRK2 (Neurotrophic tyrosine kinase, receptor, type 2) • TERT (Telomerase Reverse Transcriptase)
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EGFR mutation • NTRK2 fusion • FGFR3 fusion • TERT mutation • IDH mutation + NTRK fusion