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Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets
Lung cancer is the leading cause of cancer-related deaths in the world. Immune checkpoint inhibitors (ICI) stimulate cytotoxic lymphocyte activity against tumour cells. These agents are available for the treatment of non-small cell lung cancer (NSCLC) after failure of platinum-based therapy. One rec...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703392/ https://www.ncbi.nlm.nih.gov/pubmed/29209522 http://dx.doi.org/10.1136/esmoopen-2017-000200 |
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author | Aguiar, Pedro Nazareth De Mello, Ramon Andrade Barreto, Carmelia Maria Noia Perry, Luke Alastair Penny-Dimri, Jahan Tadokoro, Hakaru Lopes, Gilberto de Lima |
author_facet | Aguiar, Pedro Nazareth De Mello, Ramon Andrade Barreto, Carmelia Maria Noia Perry, Luke Alastair Penny-Dimri, Jahan Tadokoro, Hakaru Lopes, Gilberto de Lima |
author_sort | Aguiar, Pedro Nazareth |
collection | PubMed |
description | Lung cancer is the leading cause of cancer-related deaths in the world. Immune checkpoint inhibitors (ICI) stimulate cytotoxic lymphocyte activity against tumour cells. These agents are available for the treatment of non-small cell lung cancer (NSCLC) after failure of platinum-based therapy. One recent study has demonstrated that ICI monotherapy was superior to platinum-based chemotherapy for first-line treatment. Nevertheless, this benefit was only for a minority of the population (30%) whose tumour programmed death receptor ligand-1 (PD-L1) expression was above 50%. Therefore, several strategies are under investigation. One option for patients with PD-L1 expression lower than 50% may be the combination of ICI with platinum-based chemotherapy or with ICIs against different targets. However, all of these combinations are at an early stage of investigation and may be very expensive or toxic, producing several harmful adverse events. |
format | Online Article Text |
id | pubmed-5703392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-57033922017-12-05 Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets Aguiar, Pedro Nazareth De Mello, Ramon Andrade Barreto, Carmelia Maria Noia Perry, Luke Alastair Penny-Dimri, Jahan Tadokoro, Hakaru Lopes, Gilberto de Lima ESMO Open Review Lung cancer is the leading cause of cancer-related deaths in the world. Immune checkpoint inhibitors (ICI) stimulate cytotoxic lymphocyte activity against tumour cells. These agents are available for the treatment of non-small cell lung cancer (NSCLC) after failure of platinum-based therapy. One recent study has demonstrated that ICI monotherapy was superior to platinum-based chemotherapy for first-line treatment. Nevertheless, this benefit was only for a minority of the population (30%) whose tumour programmed death receptor ligand-1 (PD-L1) expression was above 50%. Therefore, several strategies are under investigation. One option for patients with PD-L1 expression lower than 50% may be the combination of ICI with platinum-based chemotherapy or with ICIs against different targets. However, all of these combinations are at an early stage of investigation and may be very expensive or toxic, producing several harmful adverse events. BMJ Publishing Group 2017-07-29 /pmc/articles/PMC5703392/ /pubmed/29209522 http://dx.doi.org/10.1136/esmoopen-2017-000200 Text en © European Society for Medical Oncology (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Review Aguiar, Pedro Nazareth De Mello, Ramon Andrade Barreto, Carmelia Maria Noia Perry, Luke Alastair Penny-Dimri, Jahan Tadokoro, Hakaru Lopes, Gilberto de Lima Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
title | Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
title_full | Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
title_fullStr | Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
title_full_unstemmed | Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
title_short | Immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
title_sort | immune checkpoint inhibitors for advanced non-small cell lung cancer: emerging sequencing for new treatment targets |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5703392/ https://www.ncbi.nlm.nih.gov/pubmed/29209522 http://dx.doi.org/10.1136/esmoopen-2017-000200 |
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