Indication
Solid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion
Solid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion refers to a tissue-agnostic oncologic condition characterized by malignant solid neoplasms in adult or pediatric populations that harbor an abnormal genomic rearrangement involving the NTRK1, NTRK2, or NTRK3 genes. Read more about Solid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion
5 drugs 4 manufacturers
Drugs that treat it
Common Solid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion therapies.
VITRAKVI (larotrectinib sulfate)
VITRAKVI (larotrectinib sulfate)
ROZLYTREK (entrectinib)
AUGTYRO (repotrectinib)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonSolid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion refers to a tissue-agnostic oncologic condition characterized by malignant solid neoplasms in adult or pediatric populations that harbor an abnormal genomic rearrangement involving the NTRK1, NTRK2, or NTRK3 genes.
These somatic chromosomal fusions join the kinase domain of a tropomyosin receptor kinase (TRK) protein with an unrelated upstream partner gene.
The resulting chimeric oncoprotein exhibits constitutive, ligand-independent tyrosine kinase activation, which stimulates downstream intracellular signaling cascades—such as the MAPK, PI3K/AKT, and PLC-gamma pathways—to drive uncontrolled cellular proliferation, survival, and tumorigenesis across diverse anatomical sites and histologic subtypes.
- nih.gov
Solid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion refers to a tissue-agnostic oncologic condition characterized by malignant solid neoplasms in adult or pediatric populations that harbor an abnormal genomic rearrangement involving the NTRK1, NTRK2, or NTRK3 genes
- gene.com
Solid tumor with neurotrophic receptor tyrosine kinase (NTRK) gene fusion refers to a tissue-agnostic oncologic condition characterized by malignant solid neoplasms in adult or pediatric populations that harbor an abnormal genomic rearrangement involving the NTRK1, NTRK2, or NTRK3 genes These somatic chromosomal fusions join the kinase domain of a tropomyosin receptor kinase (TRK) protein with an unrelated upstream partner gene The resulting chimeric oncoprotein exhibits constitutive, ligand-ind...
- ucla.edu
The resulting chimeric oncoprotein exhibits constitutive, ligand-independent tyrosine kinase activation, which stimulates downstream intracellular signaling cascades—such as the MAPK, PI3K/AKT, and PLC-gamma pathways—to drive uncontrolled cellular proliferation, survival, and tumorigenesis across diverse anatomical sites and histologic subtypes
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