Annotation Detail
Information
- Associated Genes
- ALK
- Associated Variants
- ALK EML4-ALK
- Associated Disease
- lung non-small cell carcinoma
- Source Database
- CIViC Evidence
- Description
- EML4-ALK variant 1 containing H-3122 NSCLC cells were treated with second generation ALK inhibitor PF-06463922. PF-06463922 was 125x more potent at reducing cell viability than crizotinib. Control neuroblastoma cell lines with wild-type ALK did not show inhibition below 3800 nM with either drug. At values of 10 and 100 nM, PF-06463922 showed increased ability to inhibit ALK 1278 tyrosine phosphorylation in H3122 cells.
- Variant Origin
- somatic
- Variant Origin
- Somatic
- Evidence URL
- https://civic.genome.wustl.edu/links/evidence_items/1332
- Gene URL
- https://civic.genome.wustl.edu/links/genes/1
- Variant URL
- https://civic.genome.wustl.edu/links/variants/5
- Rating
- 2
- Evidence Type
- Predictive
- Disease
- Lung Non-small Cell Carcinoma
- Evidence Direction
- Supports
- Drug
- Lorlatinib
- Evidence Level
- D
- Clinical Significance
- Sensitivity/Response
- Pubmed
- 26554404
Drugs
Drug Name | Sensitivity | Supported |
---|---|---|
Lorlatinib | Sensitivity | true |