Current challenges in applying gene-driven therapies in clinical lung cancer practice

dc.contributor.authorSaarenheimo Jatta
dc.contributor.authorAndersen Heidi
dc.contributor.authorEigeliene Natalja
dc.contributor.authorJekunen Antti P.
dc.contributor.organizationfi=biolääketieteen laitos|en=Institute of Biomedicine|
dc.contributor.organizationfi=kliininen syöpätautioppi|en=Clinical Oncology|
dc.contributor.organization-code1.2.246.10.2458963.20.74978886054
dc.contributor.organization-code1.2.246.10.2458963.20.77952289591
dc.converis.publication-id67223188
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/67223188
dc.date.accessioned2022-10-28T13:32:19Z
dc.date.available2022-10-28T13:32:19Z
dc.description.abstractOver 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.<p></p>
dc.format.pagerange656
dc.format.pagerange663
dc.identifier.jour-issn2218-4333
dc.identifier.olddbid182774
dc.identifier.oldhandle10024/165868
dc.identifier.urihttps://www.utupub.fi/handle/11111/40148
dc.identifier.urnURN:NBN:fi-fe2021093048532
dc.language.isoen
dc.okm.affiliatedauthorEigeliene, Natalja
dc.okm.affiliatedauthorJekunen, Antti
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherBAISHIDENG PUBLISHING GROUP INC
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.5306/wjco.v12.i8.656
dc.relation.ispartofjournalWorld Journal of Clinical Oncology
dc.relation.issue8
dc.relation.volume12
dc.source.identifierhttps://www.utupub.fi/handle/10024/165868
dc.titleCurrent challenges in applying gene-driven therapies in clinical lung cancer practice
dc.year.issued2021

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