CPC A61K 31/5025 (2013.01) [A61K 31/404 (2013.01); A61K 31/435 (2013.01); A61K 31/4412 (2013.01); A61K 31/4439 (2013.01); A61K 31/47 (2013.01); A61K 31/496 (2013.01); A61K 31/498 (2013.01); A61K 31/506 (2013.01); A61K 31/517 (2013.01); A61K 31/519 (2013.01); A61K 31/53 (2013.01); A61K 31/5383 (2013.01); A61K 31/553 (2013.01); A61K 45/06 (2013.01); C07K 14/705 (2013.01); C07K 14/71 (2013.01); C07K 16/40 (2013.01); C12N 9/12 (2013.01); C12N 15/1137 (2013.01); C12Q 1/6883 (2013.01); C12Q 1/6886 (2013.01); C12Y 207/10001 (2013.01); G01N 33/573 (2013.01); C07K 2319/00 (2013.01); C12N 2310/11 (2013.01); C12N 2310/12 (2013.01); C12N 2310/14 (2013.01); C12Q 2600/156 (2013.01); C12Q 2600/158 (2013.01); G01N 2333/912 (2013.01); G01N 2500/04 (2013.01)] | 24 Claims |
1. A method of determining presence of a fibroblast growth factor receptor (FGFR) gene fusion or a neurotrophic tyrosine receptor kinase (NTRK) gene fusion, comprising:
detecting an FGFR or NTRK gene fusion in an FGFR or NTRK nucleic acid molecule or polypeptide in a sample obtained from a subject that has or is at risk of having a cholangiocarcinoma, thereby determining that the FGFR or NTRK gene fusion is present in the sample; and
responsive to the determination of the presence of the FGFR or NTRK gene fusion in the sample, generating a report comprising one or more therapeutic options comprising a therapeutic agent that antagonizes or inhibits an FGFR gene or gene product or an NTRK gene or gene product.
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