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Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come

Diagnostic and treatment algorithms in non-small cell lung cancer (NSCLC) are evolving at a never-before-seen pace. Histological subtyping to maximise treatment efficacy and avoid toxicity has marked the beginning of the revolution, opening the way to molecular characterisation to guide genomically...

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Detalles Bibliográficos
Autores principales: Toschi, Luca, Rossi, Sabrina, Finocchiaro, Giovanna, Santoro, Armando
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718252/
https://www.ncbi.nlm.nih.gov/pubmed/29225694
http://dx.doi.org/10.3332/ecancer.2017.787
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author Toschi, Luca
Rossi, Sabrina
Finocchiaro, Giovanna
Santoro, Armando
author_facet Toschi, Luca
Rossi, Sabrina
Finocchiaro, Giovanna
Santoro, Armando
author_sort Toschi, Luca
collection PubMed
description Diagnostic and treatment algorithms in non-small cell lung cancer (NSCLC) are evolving at a never-before-seen pace. Histological subtyping to maximise treatment efficacy and avoid toxicity has marked the beginning of the revolution, opening the way to molecular characterisation to guide genomically driven treatments with targeted agents, led by Epidermal Growth Factor Receptor (EGFR) and Anaplastic Lymphoma Kinase (ALK) inhibitors. More recently, agents against the Program Death 1 receptor (PD-1) and ligand 1 (PD-L1) have entered the clinical arena, offering new hope to NSCLC patients, although several uncertainties remain to be elucidated. Here, we review the most clinically relevant advances in the diagnosis and treatment of NSCLC in the past decade.
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spelling pubmed-57182522017-12-08 Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come Toschi, Luca Rossi, Sabrina Finocchiaro, Giovanna Santoro, Armando Ecancermedicalscience Review Diagnostic and treatment algorithms in non-small cell lung cancer (NSCLC) are evolving at a never-before-seen pace. Histological subtyping to maximise treatment efficacy and avoid toxicity has marked the beginning of the revolution, opening the way to molecular characterisation to guide genomically driven treatments with targeted agents, led by Epidermal Growth Factor Receptor (EGFR) and Anaplastic Lymphoma Kinase (ALK) inhibitors. More recently, agents against the Program Death 1 receptor (PD-1) and ligand 1 (PD-L1) have entered the clinical arena, offering new hope to NSCLC patients, although several uncertainties remain to be elucidated. Here, we review the most clinically relevant advances in the diagnosis and treatment of NSCLC in the past decade. Cancer Intelligence 2017-11-30 /pmc/articles/PMC5718252/ /pubmed/29225694 http://dx.doi.org/10.3332/ecancer.2017.787 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Toschi, Luca
Rossi, Sabrina
Finocchiaro, Giovanna
Santoro, Armando
Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
title Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
title_full Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
title_fullStr Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
title_full_unstemmed Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
title_short Non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
title_sort non-small cell lung cancer treatment (r)evolution: ten years of advances and more to come
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5718252/
https://www.ncbi.nlm.nih.gov/pubmed/29225694
http://dx.doi.org/10.3332/ecancer.2017.787
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