Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation?
Descripción del Articulo
Non–small cell lung cancer (NSCLC) remains one of the leading causes of cancer-related mortality worldwide. The identification of actionable mutations, particularly in the epidermal growth factor receptor (EGFR) gene, has substantially reshaped the therapeutic landscape of this disease. Tyrosine kin...
| Autores: | , , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2026 |
| Institución: | Colegio Médico del Perú |
| Repositorio: | Acta Médica Peruana |
| Lenguaje: | español |
| OAI Identifier: | oai:amp.cmp.org.pe:article/3495 |
| Enlace del recurso: | https://amp.cmp.org.pe/index.php/AMP/article/view/3495 |
| Nivel de acceso: | acceso abierto |
| Materia: | Neoplasias Pulmonares Carcinoma de Pulmón de Células no Pequeñas Receptores ErbB Inhibidor de la Tirosina Quinasa Resistencia a Antineoplásicos Lung Neoplasms Non-Small-Cell Lung Carcinoma ErbB Receptors, Tyrosine Kinase Inhibitors Neoplasm Drug Resistance |
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Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? ¿Dónde estamos y hacia dónde vamos en el cáncer de pulmón de células no pequeñas avanzado con mutación EGFR? |
| title |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? |
| spellingShingle |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? Meza-Liviapoma, Jessica Neoplasias Pulmonares Carcinoma de Pulmón de Células no Pequeñas Receptores ErbB Inhibidor de la Tirosina Quinasa Resistencia a Antineoplásicos Lung Neoplasms Non-Small-Cell Lung Carcinoma ErbB Receptors, Tyrosine Kinase Inhibitors Neoplasm Drug Resistance |
| title_short |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? |
| title_full |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? |
| title_fullStr |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? |
| title_full_unstemmed |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? |
| title_sort |
Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation? |
| dc.creator.none.fl_str_mv |
Meza-Liviapoma, Jessica Roque, Katia Gálvez-Niño, Marco Ruiz, Rossana Coanqui, Ofelia Valdiviezo, Natalia Olivera, Mivael Mas, Luis Meza-Liviapoma, Jessica Roque, Katia Gálvez-Niño, Marco Ruiz, Rossana Coanqui, Ofelia Valdiviezo, Natalia Olivera, Mivael Mas, Luis |
| author |
Meza-Liviapoma, Jessica |
| author_facet |
Meza-Liviapoma, Jessica Roque, Katia Gálvez-Niño, Marco Ruiz, Rossana Coanqui, Ofelia Valdiviezo, Natalia Olivera, Mivael Mas, Luis |
| author_role |
author |
| author2 |
Roque, Katia Gálvez-Niño, Marco Ruiz, Rossana Coanqui, Ofelia Valdiviezo, Natalia Olivera, Mivael Mas, Luis |
| author2_role |
author author author author author author author |
| dc.subject.none.fl_str_mv |
Neoplasias Pulmonares Carcinoma de Pulmón de Células no Pequeñas Receptores ErbB Inhibidor de la Tirosina Quinasa Resistencia a Antineoplásicos Lung Neoplasms Non-Small-Cell Lung Carcinoma ErbB Receptors, Tyrosine Kinase Inhibitors Neoplasm Drug Resistance |
| topic |
Neoplasias Pulmonares Carcinoma de Pulmón de Células no Pequeñas Receptores ErbB Inhibidor de la Tirosina Quinasa Resistencia a Antineoplásicos Lung Neoplasms Non-Small-Cell Lung Carcinoma ErbB Receptors, Tyrosine Kinase Inhibitors Neoplasm Drug Resistance |
| description |
Non–small cell lung cancer (NSCLC) remains one of the leading causes of cancer-related mortality worldwide. The identification of actionable mutations, particularly in the epidermal growth factor receptor (EGFR) gene, has substantially reshaped the therapeutic landscape of this disease. Tyrosine kinase inhibitors (TKIs) have consistently demonstrated improvements in progression-free survival and overall survival compared with conventional chemotherapy. However, acquired resistance inevitably develops in most patients, driven by secondary mutations, activation of alternative signaling pathways such as MET or HER2, or histologic transformation. In recent years, the management of EGFR-mutatedNSCLC has evolved toward more complex strategies, including first-line combination approaches, treatment intensification with chemotherapy, and the use of bispecific antibodies. In addition, targeted therapies have been developed for uncommon mutations, such as exon 20 insertions, and more recently, antibody-drug conjugates have expanded therapeutic options in the post-osimertinib setting. The objective of this review is to provide an updated overview of the current treatment landscape for advanced EGFR-mutated NSCLC and to discuss emerging strategies aimed at overcoming resistance mechanisms. |
| publishDate |
2026 |
| dc.date.none.fl_str_mv |
2026-05-26 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
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publishedVersion |
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https://amp.cmp.org.pe/index.php/AMP/article/view/3495 10.35663/amp.2026.431.3495 |
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https://amp.cmp.org.pe/index.php/AMP/article/view/3495 |
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10.35663/amp.2026.431.3495 |
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spa |
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spa |
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https://amp.cmp.org.pe/index.php/AMP/article/view/3495/2055 |
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https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0 |
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openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
Colegio Médico del Perú |
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Colegio Médico del Perú |
| dc.source.none.fl_str_mv |
ACTA MEDICA PERUANA; Vol. 43 No. 1 (2026): January - March ACTA MEDICA PERUANA; Vol. 43 Núm. 1 (2026): Enero - Marzo 1728-5917 1018-8800 reponame:Acta Médica Peruana instname:Colegio Médico del Perú instacron:CMP |
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Colegio Médico del Perú |
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CMP |
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CMP |
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Acta Médica Peruana |
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Acta Médica Peruana |
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1868077761364492288 |
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Where are we and where are we going in advanced non-small cell lung cancer with EGFR mutation?¿Dónde estamos y hacia dónde vamos en el cáncer de pulmón de células no pequeñas avanzado con mutación EGFR?Meza-Liviapoma, JessicaRoque, KatiaGálvez-Niño, MarcoRuiz, RossanaCoanqui, OfeliaValdiviezo, NataliaOlivera, MivaelMas, LuisMeza-Liviapoma, JessicaRoque, KatiaGálvez-Niño, MarcoRuiz, RossanaCoanqui, OfeliaValdiviezo, NataliaOlivera, MivaelMas, LuisNeoplasias PulmonaresCarcinoma de Pulmón de Células no PequeñasReceptores ErbB Inhibidor de la Tirosina QuinasaResistencia a AntineoplásicosLung NeoplasmsNon-Small-Cell Lung CarcinomaErbB Receptors, Tyrosine Kinase InhibitorsNeoplasm Drug ResistanceNon–small cell lung cancer (NSCLC) remains one of the leading causes of cancer-related mortality worldwide. The identification of actionable mutations, particularly in the epidermal growth factor receptor (EGFR) gene, has substantially reshaped the therapeutic landscape of this disease. Tyrosine kinase inhibitors (TKIs) have consistently demonstrated improvements in progression-free survival and overall survival compared with conventional chemotherapy. However, acquired resistance inevitably develops in most patients, driven by secondary mutations, activation of alternative signaling pathways such as MET or HER2, or histologic transformation. In recent years, the management of EGFR-mutatedNSCLC has evolved toward more complex strategies, including first-line combination approaches, treatment intensification with chemotherapy, and the use of bispecific antibodies. In addition, targeted therapies have been developed for uncommon mutations, such as exon 20 insertions, and more recently, antibody-drug conjugates have expanded therapeutic options in the post-osimertinib setting. The objective of this review is to provide an updated overview of the current treatment landscape for advanced EGFR-mutated NSCLC and to discuss emerging strategies aimed at overcoming resistance mechanisms.El cáncer de pulmón de células no pequeñas (CPCNP) continúa siendo una de las principales causas de mortalidad por cáncer a nivel mundial. La identificación de mutaciones accionables, en especial en el gen del receptor del factor de crecimiento epidérmico (EGFR), ha modificado de manera sustancial el abordaje terapéutico de esta enfermedad. Los Inhibidores de tirosina quinasa (TKI) han demostrado mejoras consistentes en supervivencia libre de progresión y supervivencia global frente a la quimioterapia convencional. No obstante, la resistencia adquirida se desarrolla en la mayoría de los casos, ya sea por mutaciones secundarias, activación de vías alternativas como MET o HER2, o transformación histológica. En los últimos años, el manejo del CPCNP con mutación EGFR ha evolucionado hacia estrategias más complejas que incluyen combinaciones en primera línea, esquemas de intensificación con quimioterapia y el uso de anticuerpos biespecíficos. Asimismo, se han desarrollado terapias dirigidas específicas para mutaciones no frecuentes, como las inserciones del exón 20, y recientemente los anticuerpos fármaco-conjugados han ampliado las alternativas terapéuticas en el escenario pososimertinib. El objetivo de esta revisión es actualizar el estado actual del tratamiento del CPCNP avanzado con mutación EGFR y discutir las estrategias emergentes orientadas a superar los mecanismos de resistencia.Colegio Médico del Perú2026-05-26info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://amp.cmp.org.pe/index.php/AMP/article/view/349510.35663/amp.2026.431.3495ACTA MEDICA PERUANA; Vol. 43 No. 1 (2026): January - MarchACTA MEDICA PERUANA; Vol. 43 Núm. 1 (2026): Enero - Marzo1728-59171018-8800reponame:Acta Médica Peruanainstname:Colegio Médico del Perúinstacron:CMPspahttps://amp.cmp.org.pe/index.php/AMP/article/view/3495/2055Copyright (c) 2026 Jessica Meza-Liviapoma, Katia Roque, Marco Gálvez-Niño, Rossana Ruiz, Ofelia Coanqui, Natalia Valdiviezo, Mivael Olivera, Luis Mashttps://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessoai:amp.cmp.org.pe:article/34952026-05-27T20:47:36Z |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).
La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).