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- W2896424462 endingPage "747" @default.
- W2896424462 startingPage "731" @default.
- W2896424462 abstract "NTRK gene fusions involving either NTRK1, NTRK2 or NTRK3 (encoding the neurotrophin receptors TRKA, TRKB and TRKC, respectively) are oncogenic drivers of various adult and paediatric tumour types. These fusions can be detected in the clinic using a variety of methods, including tumour DNA and RNA sequencing and plasma cell-free DNA profiling. The treatment of patients with NTRK fusion-positive cancers with a first-generation TRK inhibitor, such as larotrectinib or entrectinib, is associated with high response rates (>75%), regardless of tumour histology. First-generation TRK inhibitors are well tolerated by most patients, with toxicity profiles characterized by occasional off-tumour, on-target adverse events (attributable to TRK inhibition in non-malignant tissues). Despite durable disease control in many patients, advanced-stage NTRK fusion-positive cancers eventually become refractory to TRK inhibition; resistance can be mediated by the acquisition of NTRK kinase domain mutations. Fortunately, certain resistance mutations can be overcome by second-generation TRK inhibitors, including LOXO-195 and TPX-0005 that are being explored in clinical trials. In this Review, we discuss the biology of NTRK fusions, strategies to target these drivers in the treatment-naive and acquired-resistance disease settings, and the unique safety profile of TRK inhibitors." @default.
- W2896424462 created "2018-10-26" @default.
- W2896424462 creator A5002819777 @default.
- W2896424462 creator A5041993659 @default.
- W2896424462 creator A5063199354 @default.
- W2896424462 date "2018-10-17" @default.
- W2896424462 modified "2023-10-17" @default.
- W2896424462 title "NTRK fusion-positive cancers and TRK inhibitor therapy" @default.
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