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Updated moalmanac db to v.2023-04-06
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brendanreardon committed Apr 13, 2023
1 parent 09fab94 commit 56fe007
Showing 1 changed file with 36 additions and 1 deletion.
37 changes: 36 additions & 1 deletion moalmanac/datasources/moalmanac/molecular-oncology-almanac.json
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{
"release": "v.2023-02-02",
"release": "v.2023-04-06",
"version": "1.0.0",
"genes": [
"ABL1",
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"nct": "",
"last_updated": "2/2/23",
"feature_display": "ESR1"
},
{
"feature_type": "Somatic Variant",
"gene": "BRAF",
"chromosome": "7",
"start_position": 140453136,
"end_position": 140453136,
"reference_allele": "A",
"alternate_allele": "T",
"cdna_change": "c.1799T>A",
"protein_change": "p.V600E",
"variant_annotation": "Missense",
"exon": 15,
"rsid": "rs113488022",
"disease": "Low-grade glioma",
"context": "Unresctable or metastatic",
"oncotree_term": "Low-Grade Glioma, NOS",
"oncotree_code": "LGGNOS",
"therapy_name": "Dabrafenib + Trametinib",
"therapy_strategy": "B-RAF inhibition + MEK inhibition",
"therapy_type": "Targeted therapy",
"therapy_sensitivity": 1,
"therapy_resistance": "",
"favorable_prognosis": "",
"predictive_implication": "FDA-Approved",
"description": "The U.S. Food and Drug Administration (FDA) granted approval to dabrafenib in combination with trametinib for the treament of pediatric patients 1 year of age or older with low-grade glioma (LGG) with a BRAF V600E mutation who require systemic therapy.",
"preferred_assertion": "",
"source_type": "FDA",
"citation": "Novartis Pharmaceuticals Corporation. Tafinlar (dabrafenib) [package insert]. U.S. Food and Drug Administration website. https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/202806s025lbl.pdf. Revised March 2023. Accessed April 6, 2023.",
"url": "https://www.accessdata.fda.gov/drugsatfda_docs/label/2023/202806s025lbl.pdf",
"doi": "",
"pmid": "",
"nct": "",
"last_updated": "4/6/23",
"feature_display": "BRAF p.V600E (Missense)"
}
]
}

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