| Literature DB >> 33467570 |
D Gwyn Bebb1, Shantanu Banerji2, Normand Blais3, Patrice Desmeules4, Sharlene Gill5, Andrea Grin6, Harriet Feilotter6, Aaron R Hansen7, Martin Hyrcza8, Monika Krzyzanowska7, Barbara Melosky5, Jonathan Noujaim9, Bibiana Purgina10, Dean Ruether11, Christine E Simmons5, Denis Soulieres3, Emina Emilia Torlakovic12, Ming-Sound Tsao13.
Abstract
The tyrosine receptor kinase (TRK) inhibitors larotrectinib and entrectinib were recently approved in Canada for the treatment of solid tumours harbouring neurotrophic tyrosine receptor kinase (NTRK) gene fusions. These NTRK gene fusions are oncogenic drivers found in most tumour types at a low frequency (<5%), and at a higher frequency (>80%) in a small number of rare tumours (e.g., secretory carcinoma of the salivary gland and of the breast). They are generally mutually exclusive of other common oncogenic drivers. Larotrectinib and entrectinib have demonstrated impressive overall response rates and tolerability in Phase I/II trials in patients with TRK fusion cancer with no other effective treatment options. Given the low frequency of TRK fusion cancer and the heterogeneous molecular testing landscape in Canada, identifying and optimally managing such patients represents a new challenge. We provide a Canadian consensus on when and how to test for NTRK gene fusions and when to consider treatment with a TRK inhibitor. We focus on five tumour types: thyroid carcinoma, colorectal carcinoma, non-small cell lung carcinoma, soft tissue sarcoma, and salivary gland carcinoma. Based on the probability of the tumour harbouring an NTRK gene fusion, we also suggest a tumour-agnostic consensus for NTRK gene fusion testing and treatment. We recommend considering a TRK inhibitor in all patients with TRK fusion cancer with no other effective treatment options.Entities:
Keywords: NTRK; TRK fusion; entrectinib; larotrectinib; molecular testing; oncogenic drivers; targeted therapy; tumour-agnostic
Year: 2021 PMID: 33467570 PMCID: PMC7903287 DOI: 10.3390/curroncol28010053
Source DB: PubMed Journal: Curr Oncol ISSN: 1198-0052 Impact factor: 3.677