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Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer

INTRODUCTION: Despite durable responses from immune-checkpoint blockade (ICB) in a subset of patients with advanced non-small cell lung cancer (NSCLC), the majority of patients do not derive benefit from this treatment. In this analysis we evaluated the impact of concomitant administration of antibi...

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Autores principales: Huemer, Florian, Rinnerthaler, Gabriel, Westphal, Theresa, Hackl, Hubert, Hutarew, Georg, Gampenrieder, Simon Peter, Weiss, Lukas, Greil, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893258/
https://www.ncbi.nlm.nih.gov/pubmed/29662663
http://dx.doi.org/10.18632/oncotarget.24751
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author Huemer, Florian
Rinnerthaler, Gabriel
Westphal, Theresa
Hackl, Hubert
Hutarew, Georg
Gampenrieder, Simon Peter
Weiss, Lukas
Greil, Richard
author_facet Huemer, Florian
Rinnerthaler, Gabriel
Westphal, Theresa
Hackl, Hubert
Hutarew, Georg
Gampenrieder, Simon Peter
Weiss, Lukas
Greil, Richard
author_sort Huemer, Florian
collection PubMed
description INTRODUCTION: Despite durable responses from immune-checkpoint blockade (ICB) in a subset of patients with advanced non-small cell lung cancer (NSCLC), the majority of patients do not derive benefit from this treatment. In this analysis we evaluated the impact of concomitant administration of antibiotics during initiation of ICB on clinical outcome. METHODS: Advanced non-squamous NSCLC patients receiving ICB as second- or later line between 2015 and 2017 at our tertiary cancer center in Salzburg (Austria) were included. Concomitant use of antibiotics was defined as administration of antibiotics within a time frame of one month before or one month after initiation of ICB (AB(+)-group). RESULTS: Of the 30 patients included, 11 (36.7%) received antibiotics one month before or one month after start of ICB (AB(+)-group). Median PFS on ICB was in favor of the AB(-)-group (AB(-): 3.1 months [95%CI: 3.0-16.3]; AB(+): 2.9 months, [95%CI: 1.9-NA]; HR=0.46 [95%CI: 0.12-0.90], p=0.031). Furthermore, median OS was significantly longer in the AB(-)-group (AB(-): 15.1 months [95%CI: 11.1-NA]; AB(+): 7.5 months [95%CI: 6.3-NA]; HR=0.31 [95%CI: 0.02-0.78], p=0.026). In a multivariate analysis, the antibiotic treatment status was identified as the only parameter statistically significantly associated with PFS (p=0.028) and OS (p=0.026). CONCLUSIONS: Stratification of patients according to the antibiotic treatment status is warranted in future trials investigating ICB.
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spelling pubmed-58932582018-04-16 Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer Huemer, Florian Rinnerthaler, Gabriel Westphal, Theresa Hackl, Hubert Hutarew, Georg Gampenrieder, Simon Peter Weiss, Lukas Greil, Richard Oncotarget Research Paper INTRODUCTION: Despite durable responses from immune-checkpoint blockade (ICB) in a subset of patients with advanced non-small cell lung cancer (NSCLC), the majority of patients do not derive benefit from this treatment. In this analysis we evaluated the impact of concomitant administration of antibiotics during initiation of ICB on clinical outcome. METHODS: Advanced non-squamous NSCLC patients receiving ICB as second- or later line between 2015 and 2017 at our tertiary cancer center in Salzburg (Austria) were included. Concomitant use of antibiotics was defined as administration of antibiotics within a time frame of one month before or one month after initiation of ICB (AB(+)-group). RESULTS: Of the 30 patients included, 11 (36.7%) received antibiotics one month before or one month after start of ICB (AB(+)-group). Median PFS on ICB was in favor of the AB(-)-group (AB(-): 3.1 months [95%CI: 3.0-16.3]; AB(+): 2.9 months, [95%CI: 1.9-NA]; HR=0.46 [95%CI: 0.12-0.90], p=0.031). Furthermore, median OS was significantly longer in the AB(-)-group (AB(-): 15.1 months [95%CI: 11.1-NA]; AB(+): 7.5 months [95%CI: 6.3-NA]; HR=0.31 [95%CI: 0.02-0.78], p=0.026). In a multivariate analysis, the antibiotic treatment status was identified as the only parameter statistically significantly associated with PFS (p=0.028) and OS (p=0.026). CONCLUSIONS: Stratification of patients according to the antibiotic treatment status is warranted in future trials investigating ICB. Impact Journals LLC 2018-03-27 /pmc/articles/PMC5893258/ /pubmed/29662663 http://dx.doi.org/10.18632/oncotarget.24751 Text en Copyright: © 2018 Huemer et al. 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/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Huemer, Florian
Rinnerthaler, Gabriel
Westphal, Theresa
Hackl, Hubert
Hutarew, Georg
Gampenrieder, Simon Peter
Weiss, Lukas
Greil, Richard
Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
title Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
title_full Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
title_fullStr Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
title_full_unstemmed Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
title_short Impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
title_sort impact of antibiotic treatment on immune-checkpoint blockade efficacy in advanced non-squamous non-small cell lung cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893258/
https://www.ncbi.nlm.nih.gov/pubmed/29662663
http://dx.doi.org/10.18632/oncotarget.24751
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