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How I treat NTRK gene fusion-positive cancers

NTRK fusions are found at low frequencies (commonly <1%) in a range of common tumour types and at high frequencies (up to or greater than 90%) in rare cancer types (secretory breast carcinoma, mammary analogue secretory carcinoma and infantile fibrosarcoma). The fusions typically occur in a mutua...

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Detalles Bibliográficos
Autor principal: Lassen, Ulrik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890394/
https://www.ncbi.nlm.nih.gov/pubmed/31803506
http://dx.doi.org/10.1136/esmoopen-2019-000612
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author Lassen, Ulrik
author_facet Lassen, Ulrik
author_sort Lassen, Ulrik
collection PubMed
description NTRK fusions are found at low frequencies (commonly <1%) in a range of common tumour types and at high frequencies (up to or greater than 90%) in rare cancer types (secretory breast carcinoma, mammary analogue secretory carcinoma and infantile fibrosarcoma). The fusions typically occur in a mutually exclusive fashion with other strong mitogenic drivers, and it is of significant importance to identify patients in order to offer transformative treatment with TRK inhibitors. Larotractinib or entrectinib have resulted in fast and durable response with few and reversible adverse events. Even though on-target resistance may occur, second generation TRK inhibitors are in development and have shown promising activity. Diagnostic strategies must be applied, considering available assays and specific tumour types.
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spelling pubmed-68903942019-12-04 How I treat NTRK gene fusion-positive cancers Lassen, Ulrik ESMO Open Review NTRK fusions are found at low frequencies (commonly <1%) in a range of common tumour types and at high frequencies (up to or greater than 90%) in rare cancer types (secretory breast carcinoma, mammary analogue secretory carcinoma and infantile fibrosarcoma). The fusions typically occur in a mutually exclusive fashion with other strong mitogenic drivers, and it is of significant importance to identify patients in order to offer transformative treatment with TRK inhibitors. Larotractinib or entrectinib have resulted in fast and durable response with few and reversible adverse events. Even though on-target resistance may occur, second generation TRK inhibitors are in development and have shown promising activity. Diagnostic strategies must be applied, considering available assays and specific tumour types. BMJ Publishing Group 2019-11-25 /pmc/articles/PMC6890394/ /pubmed/31803506 http://dx.doi.org/10.1136/esmoopen-2019-000612 Text en © Author (s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, any changes made are indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Review
Lassen, Ulrik
How I treat NTRK gene fusion-positive cancers
title How I treat NTRK gene fusion-positive cancers
title_full How I treat NTRK gene fusion-positive cancers
title_fullStr How I treat NTRK gene fusion-positive cancers
title_full_unstemmed How I treat NTRK gene fusion-positive cancers
title_short How I treat NTRK gene fusion-positive cancers
title_sort how i treat ntrk gene fusion-positive cancers
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890394/
https://www.ncbi.nlm.nih.gov/pubmed/31803506
http://dx.doi.org/10.1136/esmoopen-2019-000612
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