EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins

Although targeted therapy is standard of care in a large subset of oncogenic addicted non-small cell lung cancers (NSCLC), until recently, this therapeutic approach has not been feasible for all genomic alterations such as for those tumors harboring Epidermal Growth Factor Receptor (EGFR) exon 20 in...

Full description

Autores:
Remón, Jordi
Hendriks, Lizza E.L
Cardona-Mendoza, Andrés Felipe
Tipo de recurso:
Article of journal
Fecha de publicación:
2020
Institución:
Universidad El Bosque
Repositorio:
Repositorio U. El Bosque
Idioma:
eng
OAI Identifier:
oai:repositorio.unbosque.edu.co:20.500.12495/4440
Acceso en línea:
http://hdl.handle.net/20.500.12495/4440
https://doi.org/10.1016/j.ctrv.2020.102105
Palabra clave:
EGFR exon 20 insertions
Poziotinib
TAK-788
Amivantamab
Osimertinib
Rights
openAccess
License
Acceso abierto
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oai_identifier_str oai:repositorio.unbosque.edu.co:20.500.12495/4440
network_acronym_str UNBOSQUE2
network_name_str Repositorio U. El Bosque
repository_id_str
dc.title.spa.fl_str_mv EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
dc.title.translated.spa.fl_str_mv EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
title EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
spellingShingle EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
EGFR exon 20 insertions
Poziotinib
TAK-788
Amivantamab
Osimertinib
title_short EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
title_full EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
title_fullStr EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
title_full_unstemmed EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
title_sort EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history begins
dc.creator.fl_str_mv Remón, Jordi
Hendriks, Lizza E.L
Cardona-Mendoza, Andrés Felipe
dc.contributor.author.none.fl_str_mv Remón, Jordi
Hendriks, Lizza E.L
Cardona-Mendoza, Andrés Felipe
dc.contributor.orcid.none.fl_str_mv Cardona-Mendoza, Andrés Felipe [0000-0002-6697-5471]
dc.subject.keywords.spa.fl_str_mv EGFR exon 20 insertions
Poziotinib
TAK-788
Amivantamab
Osimertinib
topic EGFR exon 20 insertions
Poziotinib
TAK-788
Amivantamab
Osimertinib
description Although targeted therapy is standard of care in a large subset of oncogenic addicted non-small cell lung cancers (NSCLC), until recently, this therapeutic approach has not been feasible for all genomic alterations such as for those tumors harboring Epidermal Growth Factor Receptor (EGFR) exon 20 insertion (ex20ins) mutations. Despite being the third most common EGFR mutation, a limited efficacy of first- and second-generation EGFR tyrosine kinase inhibitors (TKI) exists. This is related to the heterogeneity at the molecular level in EGFR ex20ins mutation variants and the finding that this mutation promotes active kinase conformation but does not increase the affinity for EGFR TKI. As a result, the prognosis of this population is diminished. Therefore, chemotherapy remained the most suitable strategy in this subset of EGFR mutant NSCLC patients. Recently, new treatment strategies have been reported in this landscape, either with new EGFR TKI or bispecific antibodies, which may establish a new standard of care in the coming future for these patients. Future research should focus on elucidating the oncogenic degree of all EGFR ex20ins variants, the potential role of combination strategies either with chemotherapy or immune checkpoint inhibitors, and the most appropriate first-line treatment strategy in this subgroup. Finally, the knowledge of mechanisms of acquired resistance to these new agents upon progression is a priority for personalising treatment at that time. It is in this framework, that we provide a thorough overview on this subject.
publishDate 2020
dc.date.accessioned.none.fl_str_mv 2020-10-14T23:01:38Z
dc.date.available.none.fl_str_mv 2020-10-14T23:01:38Z
dc.date.issued.none.fl_str_mv 2020
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dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.local.none.fl_str_mv Artículo de revista
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dc.identifier.issn.none.fl_str_mv 0305-7378
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/20.500.12495/4440
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.ctrv.2020.102105
dc.identifier.instname.spa.fl_str_mv instname:Universidad El Bosque
dc.identifier.reponame.spa.fl_str_mv reponame:Repositorio Institucional Universidad El Bosque
dc.identifier.repourl.none.fl_str_mv repourl:https://repositorio.unbosque.edu.co
identifier_str_mv 0305-7378
instname:Universidad El Bosque
reponame:Repositorio Institucional Universidad El Bosque
repourl:https://repositorio.unbosque.edu.co
url http://hdl.handle.net/20.500.12495/4440
https://doi.org/10.1016/j.ctrv.2020.102105
dc.language.iso.none.fl_str_mv eng
language eng
dc.relation.ispartofseries.spa.fl_str_mv Cancer treatment reviews, 0305-7378, Vol. 90, 2020
dc.relation.uri.none.fl_str_mv https://www.sciencedirect.com/science/article/abs/pii/S0305737220301432
dc.rights.local.spa.fl_str_mv Acceso abierto
dc.rights.accessrights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
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Acceso abierto
dc.rights.creativecommons.none.fl_str_mv 2020-11
rights_invalid_str_mv Acceso abierto
http://purl.org/coar/access_right/c_abf2
2020-11
eu_rights_str_mv openAccess
dc.format.mimetype.none.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv Elsevier
dc.publisher.journal.spa.fl_str_mv Cancer treatment reviews
institution Universidad El Bosque
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spelling Remón, JordiHendriks, Lizza E.LCardona-Mendoza, Andrés FelipeCardona-Mendoza, Andrés Felipe [0000-0002-6697-5471]2020-10-14T23:01:38Z2020-10-14T23:01:38Z20200305-7378http://hdl.handle.net/20.500.12495/4440https://doi.org/10.1016/j.ctrv.2020.102105instname:Universidad El Bosquereponame:Repositorio Institucional Universidad El Bosquerepourl:https://repositorio.unbosque.edu.coapplication/pdfengElsevierCancer treatment reviewsCancer treatment reviews, 0305-7378, Vol. 90, 2020https://www.sciencedirect.com/science/article/abs/pii/S0305737220301432EGFR exon 20 insertions in advanced non-small cell lung cancer: A new history beginsEGFR exon 20 insertions in advanced non-small cell lung cancer: A new history beginsArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85EGFR exon 20 insertionsPoziotinibTAK-788AmivantamabOsimertinibAlthough targeted therapy is standard of care in a large subset of oncogenic addicted non-small cell lung cancers (NSCLC), until recently, this therapeutic approach has not been feasible for all genomic alterations such as for those tumors harboring Epidermal Growth Factor Receptor (EGFR) exon 20 insertion (ex20ins) mutations. Despite being the third most common EGFR mutation, a limited efficacy of first- and second-generation EGFR tyrosine kinase inhibitors (TKI) exists. This is related to the heterogeneity at the molecular level in EGFR ex20ins mutation variants and the finding that this mutation promotes active kinase conformation but does not increase the affinity for EGFR TKI. As a result, the prognosis of this population is diminished. Therefore, chemotherapy remained the most suitable strategy in this subset of EGFR mutant NSCLC patients. Recently, new treatment strategies have been reported in this landscape, either with new EGFR TKI or bispecific antibodies, which may establish a new standard of care in the coming future for these patients. Future research should focus on elucidating the oncogenic degree of all EGFR ex20ins variants, the potential role of combination strategies either with chemotherapy or immune checkpoint inhibitors, and the most appropriate first-line treatment strategy in this subgroup. Finally, the knowledge of mechanisms of acquired resistance to these new agents upon progression is a priority for personalising treatment at that time. 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