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How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease
ROS proto-oncogene 1 (ROS1) rearrangements defines a distinct group of non-small cell lung cancer (NSCLC), mainly represented by younger subjects, never smokers and with adenocarcinoma histology. Fusions involving ROS1 gene are present in 1-2% of lung adenocarcinomas and other solid tumors. Identifi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815342/ https://www.ncbi.nlm.nih.gov/pubmed/33489827 http://dx.doi.org/10.21037/tlcr-20-1109 |
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author | Landi, Lorenza Cappuzzo, Federico |
author_facet | Landi, Lorenza Cappuzzo, Federico |
author_sort | Landi, Lorenza |
collection | PubMed |
description | ROS proto-oncogene 1 (ROS1) rearrangements defines a distinct group of non-small cell lung cancer (NSCLC), mainly represented by younger subjects, never smokers and with adenocarcinoma histology. Fusions involving ROS1 gene are present in 1-2% of lung adenocarcinomas and other solid tumors. Identification of patients harboring ROS1 rearrangements is a critical issue and current guidelines recommend screening of all advanced non-squamous NSCLC and certain squamous lung cancer patients. A number of trials have supported crizotinib as the best option for NSCLC patients with ROS1 translocations, irrespective of line of therapy. Unfortunately, the majority of patients become insensitive to crizotinib, due to the occurrence of secondary ROS1 mutations or failure within the central nervous system (CNS). Several highly potent and CNS penetrant ROS1 inhibitors have been developed and recent data highlight their potential role in the front-line treatment of this disease. Among them entrectinib, also known as RXDX-101, is a potent second-generation, multitarget oral inhibitor against the neurotrophin receptors TRKA, TRKB, TRKC ALK, and ROS1 with the ability to cross the blood-brain barrier. In the next few years, results of ongoing trials with novel ROS1 inhibitors and dedicated translational research studies might help to define the optimal sequence of treatment for ROS1-positive NSCLC patients. |
format | Online Article Text |
id | pubmed-7815342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
spelling | pubmed-78153422021-01-22 How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease Landi, Lorenza Cappuzzo, Federico Transl Lung Cancer Res Review Article on Looking for Review Article on Looking for Chimeras in NSCLC: Widen Therapeutic Options Targeting Oncogenic Fusions ROS proto-oncogene 1 (ROS1) rearrangements defines a distinct group of non-small cell lung cancer (NSCLC), mainly represented by younger subjects, never smokers and with adenocarcinoma histology. Fusions involving ROS1 gene are present in 1-2% of lung adenocarcinomas and other solid tumors. Identification of patients harboring ROS1 rearrangements is a critical issue and current guidelines recommend screening of all advanced non-squamous NSCLC and certain squamous lung cancer patients. A number of trials have supported crizotinib as the best option for NSCLC patients with ROS1 translocations, irrespective of line of therapy. Unfortunately, the majority of patients become insensitive to crizotinib, due to the occurrence of secondary ROS1 mutations or failure within the central nervous system (CNS). Several highly potent and CNS penetrant ROS1 inhibitors have been developed and recent data highlight their potential role in the front-line treatment of this disease. Among them entrectinib, also known as RXDX-101, is a potent second-generation, multitarget oral inhibitor against the neurotrophin receptors TRKA, TRKB, TRKC ALK, and ROS1 with the ability to cross the blood-brain barrier. In the next few years, results of ongoing trials with novel ROS1 inhibitors and dedicated translational research studies might help to define the optimal sequence of treatment for ROS1-positive NSCLC patients. AME Publishing Company 2020-12 /pmc/articles/PMC7815342/ /pubmed/33489827 http://dx.doi.org/10.21037/tlcr-20-1109 Text en 2020 Translational Lung Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Review Article on Looking for Review Article on Looking for Chimeras in NSCLC: Widen Therapeutic Options Targeting Oncogenic Fusions Landi, Lorenza Cappuzzo, Federico How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease |
title | How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease |
title_full | How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease |
title_fullStr | How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease |
title_full_unstemmed | How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease |
title_short | How selecting best upfront therapy for metastatic disease?—Focus on ROS1-rearranged disease |
title_sort | how selecting best upfront therapy for metastatic disease?—focus on ros1-rearranged disease |
topic | Review Article on Looking for Review Article on Looking for Chimeras in NSCLC: Widen Therapeutic Options Targeting Oncogenic Fusions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7815342/ https://www.ncbi.nlm.nih.gov/pubmed/33489827 http://dx.doi.org/10.21037/tlcr-20-1109 |
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