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BIOMARKER:

IDH wild-type

i
Other names: 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, 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
Entrez ID:
Related biomarkers:
1d
New P3 trial
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IDH1 (Isocitrate dehydrogenase (NADP(+)) 1) • MGMT (6-O-methylguanine-DNA methyltransferase)
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MGMT promoter methylation • IDH wild-type • IDH1 R132
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temozolomide
2d
New trial
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IDH1 (Isocitrate dehydrogenase (NADP(+)) 1) • IDH2 (Isocitrate Dehydrogenase (NADP(+)) 2)
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IDH wild-type
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Avastin (bevacizumab) • carboplatin • irinotecan
2d
Surgical Pembro +/- Olaparib w TMZ for rGBM (clinicaltrials.gov)
P2, N=78, Recruiting, L. Nicolas Gonzalez Castro, MD, PhD | Trial completion date: Nov 2026 --> Mar 2027 | Trial primary completion date: Feb 2026 --> Aug 2026
Trial completion date • Trial primary completion date
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EGFR (Epidermal growth factor receptor) • TERT (Telomerase Reverse Transcriptase)
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EGFR mutation • EGFR amplification • IDH wild-type
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Keytruda (pembrolizumab) • Lynparza (olaparib) • temozolomide
2d
Effect of stRess and exeRcize on the Outcome After Chemo-Radiation (clinicaltrials.gov)
P=N/A, N=42, Completed, Maastricht Radiation Oncology | Recruiting --> Completed | Trial completion date: Dec 2025 --> Mar 2026 | Trial primary completion date: Dec 2025 --> Mar 2026
Trial completion • Trial completion date • Trial primary completion date
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IDH wild-type
2d
Spatial Transcriptomics Characterisation of Radionecrotic Changes in Glioblastoma Patients. (PubMed, Neuro Oncol)
This study delineates a complex spatial architecture of brain tissue with post-treatment changes and its discrepancies from progressive GB, thus facilitating future research into novel treatment strategies.
Journal
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EGFR (Epidermal growth factor receptor)
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EGFR expression • IDH wild-type
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temozolomide
2d
CAN-201 NDG: Azeliragon and Chemoradiotherapy in Newly Diagnosed Glioblastoma (clinicaltrials.gov)
P1/2, N=18, Recruiting, Cantex Pharmaceuticals | Not yet recruiting --> Recruiting
Enrollment open
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S100A9 (S100 Calcium Binding Protein A9)
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IDH wild-type
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temozolomide • azeliragon (TTP488)
2d
Phase classification • Checkpoint inhibition
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IDH wild-type
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Yervoy (ipilimumab) • Opdualag (nivolumab/relatlimab-rmbw)
2d
Machine Learning-Based Preoperative Predicting TERT Promoter Mutation and EGFR Gene Amplification Phenotype in IDH Wild-Type Glioblastoma Using Advanced MR Habitat Imaging. (PubMed, AJNR Am J Neuroradiol)
The tumor habitat imaging model based on advanced MRI was useful for accurately predicting TERT promoter mutation and EGFR amplification status in IDH wild-type glioblastoma.
Journal
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EGFR (Epidermal growth factor receptor) • TERT (Telomerase Reverse Transcriptase)
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EGFR mutation • EGFR amplification • IDH wild-type
3d
A Study of the Treatment of Recurrent Malignant Glioma With rQNestin34.5v.2 (clinicaltrials.gov)
P1, N=62, Active, not recruiting, Dana-Farber Cancer Institute | Recruiting --> Active, not recruiting | Trial completion date: Jan 2027 --> Jan 2028 | Trial primary completion date: Jan 2026 --> Jan 2027
Enrollment closed • Trial completion date • Trial primary completion date
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IDH1 (Isocitrate dehydrogenase (NADP(+)) 1)
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IDH1 mutation • IDH wild-type • IDH1 R132
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cyclophosphamide • linoserpaturev (CAN-3110)
4d
A Study Testing the Effect of Immunotherapy (Ipilimumab and Nivolumab) in Patients With Recurrent Glioma With Elevated Mutational Burden (clinicaltrials.gov)
P2, N=37, Active, not recruiting, National Cancer Institute (NCI) | Trial completion date: May 2026 --> Dec 2026 | Trial primary completion date: May 2026 --> Dec 2026
Trial completion date • Trial primary completion date • Checkpoint inhibition • Tumor mutational burden • IO biomarker
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EGFR (Epidermal growth factor receptor) • TP53 (Tumor protein P53) • CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • TERT (Telomerase Reverse Transcriptase) • CDKN2B (Cyclin Dependent Kinase Inhibitor 2B) • ATRX (ATRX Chromatin Remodeler)
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TP53 mutation • EGFR mutation • EGFR amplification • CDKN2A deletion • IDH wild-type
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FoundationOne® CDx
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Opdivo (nivolumab) • Yervoy (ipilimumab) • ABP 206 (nivolumab biosimilar)
7d
Erlotinib Induces Cell Death by Blocking NIX-mediated Mitophagy Through Lysosomal Swelling in IDH1-mutant Cholangiocarcinoma. (PubMed, Anticancer Res)
The CCA cell line carrying an IDH mutation utilized mitophagy as a novel metabolic compensatory mechanism activated through EGFR-specific signaling. Mitophagy acted as a metabolic synthetic lethality partner to the EGFR inhibitor erlotinib. These findings strongly suggest the potential of erlotinib as a therapeutic strategy for patients with IDH1-mutant CCA.
Journal
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IDH1 (Isocitrate dehydrogenase (NADP(+)) 1) • ANXA5 (Annexin A5)
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IDH1 mutation • IDH wild-type
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erlotinib
8d
Extent of Resection and Survival in IDH-Wildtype Glioblastoma: A Dual-Center Retrospective Study. (PubMed, Medicina (Kaunas))
The absence of MGMT promoter methylation status, lack of volumetric EOR quantification (including non-contrast-enhancing/FLAIR disease), and lack of standardized functional outcome data substantially limited causal inference. Prospective studies integrating molecular stratification, volumetric resection metrics, and functional outcome assessments are warranted.
Retrospective data • Journal
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MGMT (6-O-methylguanine-DNA methyltransferase)
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MGMT promoter methylation • IDH wild-type