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Current challenges in applying gene-driven therapies in clinical lung cancer practice
Over the last twenty years, with the development of gene-driven therapies, numerous new drugs have entered clinical use. Very few of these new drugs are suitable for a large number of patients, and all require molecular genetic testing. In lung cancer, gene-targeted therapy has evolved rapidly and h...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394160/ https://www.ncbi.nlm.nih.gov/pubmed/34513599 http://dx.doi.org/10.5306/wjco.v12.i8.656 |
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author | Saarenheimo, Jatta Andersen, Heidi Eigeliene, Natalja Jekunen, Antti P |
author_facet | Saarenheimo, Jatta Andersen, Heidi Eigeliene, Natalja Jekunen, Antti P |
author_sort | Saarenheimo, Jatta |
collection | PubMed |
description | Over the last twenty years, with the development of gene-driven therapies, numerous new drugs have entered clinical use. Very few of these new drugs are suitable for a large number of patients, and all require molecular genetic testing. In lung cancer, gene-targeted therapy has evolved rapidly and has placed demands on the development of diagnostics and tissue sample preparation and logistics. Rapid diagnosis and prevalence assessment are necessary to determine the prognosis of a lung cancer patient based on the latest research findings. Therefore, the molecular-genetic diagnostic pathway must also be accelerated and matured to do the necessary analyses on small samples. Because lung cancer rebiopsy can be difficult, liquid biopsy techniques should be developed to cover more of the treatable mutations. There are obstacles related to tissue sampling, new genomic techniques and access to gene-driven cancer drugs, including their affordability. With this review and case study, we go into the obstacles faced by our clinic and discuss how to tackle these obstacles in lung cancer. We use lung cancer as an example due to its complexity, though these same obstacles are found in different cancers on a minor scale. |
format | Online Article Text |
id | pubmed-8394160 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-83941602021-09-09 Current challenges in applying gene-driven therapies in clinical lung cancer practice Saarenheimo, Jatta Andersen, Heidi Eigeliene, Natalja Jekunen, Antti P World J Clin Oncol Minireviews Over the last twenty years, with the development of gene-driven therapies, numerous new drugs have entered clinical use. Very few of these new drugs are suitable for a large number of patients, and all require molecular genetic testing. In lung cancer, gene-targeted therapy has evolved rapidly and has placed demands on the development of diagnostics and tissue sample preparation and logistics. Rapid diagnosis and prevalence assessment are necessary to determine the prognosis of a lung cancer patient based on the latest research findings. Therefore, the molecular-genetic diagnostic pathway must also be accelerated and matured to do the necessary analyses on small samples. Because lung cancer rebiopsy can be difficult, liquid biopsy techniques should be developed to cover more of the treatable mutations. There are obstacles related to tissue sampling, new genomic techniques and access to gene-driven cancer drugs, including their affordability. With this review and case study, we go into the obstacles faced by our clinic and discuss how to tackle these obstacles in lung cancer. We use lung cancer as an example due to its complexity, though these same obstacles are found in different cancers on a minor scale. Baishideng Publishing Group Inc 2021-08-24 2021-08-24 /pmc/articles/PMC8394160/ /pubmed/34513599 http://dx.doi.org/10.5306/wjco.v12.i8.656 Text en ©The Author(s) 2021. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (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 and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/ |
spellingShingle | Minireviews Saarenheimo, Jatta Andersen, Heidi Eigeliene, Natalja Jekunen, Antti P Current challenges in applying gene-driven therapies in clinical lung cancer practice |
title | Current challenges in applying gene-driven therapies in clinical lung cancer practice |
title_full | Current challenges in applying gene-driven therapies in clinical lung cancer practice |
title_fullStr | Current challenges in applying gene-driven therapies in clinical lung cancer practice |
title_full_unstemmed | Current challenges in applying gene-driven therapies in clinical lung cancer practice |
title_short | Current challenges in applying gene-driven therapies in clinical lung cancer practice |
title_sort | current challenges in applying gene-driven therapies in clinical lung cancer practice |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394160/ https://www.ncbi.nlm.nih.gov/pubmed/34513599 http://dx.doi.org/10.5306/wjco.v12.i8.656 |
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