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A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial)
BACKGROUND: Lung cancer is the leading cause of cancer deaths worldwide. Surgery, radiotherapy at conventional and high dose and chemotherapy are the mainstay for lung cancer treatment. Insufficient migration and activation of tumour specific effector T cells seem to be important reasons for inadequ...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684916/ https://www.ncbi.nlm.nih.gov/pubmed/26686362 http://dx.doi.org/10.1186/s12885-015-2006-2 |
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author | Safi, Seyer Beckhove, Philipp Warth, Arne Benner, Axel Roeder, Falk Rieken, Stefan Debus, Juergen Dienemann, Hendrik Hoffmann, Hans Huber, Peter E. |
author_facet | Safi, Seyer Beckhove, Philipp Warth, Arne Benner, Axel Roeder, Falk Rieken, Stefan Debus, Juergen Dienemann, Hendrik Hoffmann, Hans Huber, Peter E. |
author_sort | Safi, Seyer |
collection | PubMed |
description | BACKGROUND: Lung cancer is the leading cause of cancer deaths worldwide. Surgery, radiotherapy at conventional and high dose and chemotherapy are the mainstay for lung cancer treatment. Insufficient migration and activation of tumour specific effector T cells seem to be important reasons for inadequate host anti-tumour immune response. Ionizing radiation can induce a variety of immune responses. The goal of this randomized trial is to assess if a preoperative single fraction low dose radiation is able to improve anti-tumour immune response in operable early stage lung cancer. METHODS/DESIGN: This trial has been designed as an investigator-initiated, prospective, randomized, 2-armed phase II trial. Patients who are candidates for elective resection of early stage non-small cell lung cancer will be randomized into 2 arms. A total of 36 patients will be enrolled. The patients receive either 2 Gy or no radiation prescribed to their primary tumour. Radiation will be delivered by external beam radiotherapy using 3D radiotherapy or intensity-modulated radiation technique (IMRT) 7 days prior to surgical resection. The primary objective is to compare CD8+ T cell counts detected by immunohistochemistry in resected tumours following preoperative radiotherapy versus no radiotherapy. Secondary objectives include the association between CD8+ T cell counts and progression free survival, the correlation of CD8+ T cell counts quantified by immunohistochemistry and flow cytometry, local tumour control and recurrence patterns, survival, radiogenic treatment toxicity and postoperative morbidity and mortality. Further, frequencies of tumour reactive T cells in blood and bone marrow as well as whole blood cell transcriptomics and plasma-proteomics will be correlated with clinical outcome. DISCUSSION: This unique intervention combining preoperative low dose radiation and surgical removal of early stage non-small cell lung cancer is designed to address the problem of inadequate host anti-tumour immune response. If successful, this study may affect the role of radiotherapy in lung cancer treatment. TRIAL REGISTRATION: NCT02319408; Registration: December 29, 2014. |
format | Online Article Text |
id | pubmed-4684916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-46849162015-12-21 A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) Safi, Seyer Beckhove, Philipp Warth, Arne Benner, Axel Roeder, Falk Rieken, Stefan Debus, Juergen Dienemann, Hendrik Hoffmann, Hans Huber, Peter E. BMC Cancer Study Protocol BACKGROUND: Lung cancer is the leading cause of cancer deaths worldwide. Surgery, radiotherapy at conventional and high dose and chemotherapy are the mainstay for lung cancer treatment. Insufficient migration and activation of tumour specific effector T cells seem to be important reasons for inadequate host anti-tumour immune response. Ionizing radiation can induce a variety of immune responses. The goal of this randomized trial is to assess if a preoperative single fraction low dose radiation is able to improve anti-tumour immune response in operable early stage lung cancer. METHODS/DESIGN: This trial has been designed as an investigator-initiated, prospective, randomized, 2-armed phase II trial. Patients who are candidates for elective resection of early stage non-small cell lung cancer will be randomized into 2 arms. A total of 36 patients will be enrolled. The patients receive either 2 Gy or no radiation prescribed to their primary tumour. Radiation will be delivered by external beam radiotherapy using 3D radiotherapy or intensity-modulated radiation technique (IMRT) 7 days prior to surgical resection. The primary objective is to compare CD8+ T cell counts detected by immunohistochemistry in resected tumours following preoperative radiotherapy versus no radiotherapy. Secondary objectives include the association between CD8+ T cell counts and progression free survival, the correlation of CD8+ T cell counts quantified by immunohistochemistry and flow cytometry, local tumour control and recurrence patterns, survival, radiogenic treatment toxicity and postoperative morbidity and mortality. Further, frequencies of tumour reactive T cells in blood and bone marrow as well as whole blood cell transcriptomics and plasma-proteomics will be correlated with clinical outcome. DISCUSSION: This unique intervention combining preoperative low dose radiation and surgical removal of early stage non-small cell lung cancer is designed to address the problem of inadequate host anti-tumour immune response. If successful, this study may affect the role of radiotherapy in lung cancer treatment. TRIAL REGISTRATION: NCT02319408; Registration: December 29, 2014. BioMed Central 2015-12-19 /pmc/articles/PMC4684916/ /pubmed/26686362 http://dx.doi.org/10.1186/s12885-015-2006-2 Text en © Safi et al. 2015 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 | Study Protocol Safi, Seyer Beckhove, Philipp Warth, Arne Benner, Axel Roeder, Falk Rieken, Stefan Debus, Juergen Dienemann, Hendrik Hoffmann, Hans Huber, Peter E. A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) |
title | A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) |
title_full | A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) |
title_fullStr | A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) |
title_full_unstemmed | A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) |
title_short | A randomized phase II study of radiation induced immune boost in operable non-small cell lung cancer (RadImmune trial) |
title_sort | randomized phase ii study of radiation induced immune boost in operable non-small cell lung cancer (radimmune trial) |
topic | Study Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4684916/ https://www.ncbi.nlm.nih.gov/pubmed/26686362 http://dx.doi.org/10.1186/s12885-015-2006-2 |
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