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Radiotherapy enhances responses of lung cancer to CTLA-4 blockade
Formenti et al. have recently reported the clinical outcomes and translational readouts of a trial of the anti-CTLA-4 inhibitor, ipilimumab, in combination with palliative radiotherapy in 39 patients with non-small cell lung cancer. A radiological response was seen in 18% of patients and 31% of pati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404307/ https://www.ncbi.nlm.nih.gov/pubmed/30841910 http://dx.doi.org/10.1186/s40425-019-0542-z |
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author | Wilkins, Anna McDonald, Fiona Harrington, Kevin Melcher, Alan |
author_facet | Wilkins, Anna McDonald, Fiona Harrington, Kevin Melcher, Alan |
author_sort | Wilkins, Anna |
collection | PubMed |
description | Formenti et al. have recently reported the clinical outcomes and translational readouts of a trial of the anti-CTLA-4 inhibitor, ipilimumab, in combination with palliative radiotherapy in 39 patients with non-small cell lung cancer. A radiological response was seen in 18% of patients and 31% of patients experienced disease control. These clinical outcomes appear to be superior to historical studies using ipilimumab alone and suggest that radiation may have triggered systemic, so-called abscopal, immune responses in some patients. Induction of interferon-beta (IFN-β) and maximal expansion and contraction of distinct T cell receptor clones were the most significant factors predicting response. Importantly, established predictive biomarkers of response to immunotherapy alone, including the expression of PD-L1 in diagnostic biopsies and tumour mutational burden, did not predict response. The report provides important human qualification of pre-clinical mechanistic insights indicating that abscopal responses can be generated with optimised radiotherapy fractionation schedules and anti-CTLA-4 inhibition. Additionally, an intriguing mechanism by which radiation can be immunogenic is described, namely radiation-induced transcriptional upregulation of neo-antigens. |
format | Online Article Text |
id | pubmed-6404307 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64043072019-03-18 Radiotherapy enhances responses of lung cancer to CTLA-4 blockade Wilkins, Anna McDonald, Fiona Harrington, Kevin Melcher, Alan J Immunother Cancer Commentary Formenti et al. have recently reported the clinical outcomes and translational readouts of a trial of the anti-CTLA-4 inhibitor, ipilimumab, in combination with palliative radiotherapy in 39 patients with non-small cell lung cancer. A radiological response was seen in 18% of patients and 31% of patients experienced disease control. These clinical outcomes appear to be superior to historical studies using ipilimumab alone and suggest that radiation may have triggered systemic, so-called abscopal, immune responses in some patients. Induction of interferon-beta (IFN-β) and maximal expansion and contraction of distinct T cell receptor clones were the most significant factors predicting response. Importantly, established predictive biomarkers of response to immunotherapy alone, including the expression of PD-L1 in diagnostic biopsies and tumour mutational burden, did not predict response. The report provides important human qualification of pre-clinical mechanistic insights indicating that abscopal responses can be generated with optimised radiotherapy fractionation schedules and anti-CTLA-4 inhibition. Additionally, an intriguing mechanism by which radiation can be immunogenic is described, namely radiation-induced transcriptional upregulation of neo-antigens. BioMed Central 2019-03-06 /pmc/articles/PMC6404307/ /pubmed/30841910 http://dx.doi.org/10.1186/s40425-019-0542-z Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Commentary Wilkins, Anna McDonald, Fiona Harrington, Kevin Melcher, Alan Radiotherapy enhances responses of lung cancer to CTLA-4 blockade |
title | Radiotherapy enhances responses of lung cancer to CTLA-4 blockade |
title_full | Radiotherapy enhances responses of lung cancer to CTLA-4 blockade |
title_fullStr | Radiotherapy enhances responses of lung cancer to CTLA-4 blockade |
title_full_unstemmed | Radiotherapy enhances responses of lung cancer to CTLA-4 blockade |
title_short | Radiotherapy enhances responses of lung cancer to CTLA-4 blockade |
title_sort | radiotherapy enhances responses of lung cancer to ctla-4 blockade |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6404307/ https://www.ncbi.nlm.nih.gov/pubmed/30841910 http://dx.doi.org/10.1186/s40425-019-0542-z |
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