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Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial

BACKGROUND: Radiotherapy, preferably combined with chemotherapy, is the treatment standard for locally advanced, unresectable non-small cell lung cancer (NSCLC). The tumor response to different therapy protocols is variable, with hypoxia known to be a major factor that negatively influences treatmen...

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Autores principales: Askoxylakis, Vasileios, Dinkel, Julien, Eichinger, Monika, Stieltjes, Bram, Sommer, Gregor, Strauss, Ludwig G, Dimitrakopoulou-Strauss, Antonia, Kopp-Schneider, Annette, Haberkorn, Uwe, Huber, Peter E, Bischof, Marc, Debus, Jürgen, Thieke, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503648/
https://www.ncbi.nlm.nih.gov/pubmed/22974533
http://dx.doi.org/10.1186/1748-717X-7-157
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author Askoxylakis, Vasileios
Dinkel, Julien
Eichinger, Monika
Stieltjes, Bram
Sommer, Gregor
Strauss, Ludwig G
Dimitrakopoulou-Strauss, Antonia
Kopp-Schneider, Annette
Haberkorn, Uwe
Huber, Peter E
Bischof, Marc
Debus, Jürgen
Thieke, Christian
author_facet Askoxylakis, Vasileios
Dinkel, Julien
Eichinger, Monika
Stieltjes, Bram
Sommer, Gregor
Strauss, Ludwig G
Dimitrakopoulou-Strauss, Antonia
Kopp-Schneider, Annette
Haberkorn, Uwe
Huber, Peter E
Bischof, Marc
Debus, Jürgen
Thieke, Christian
author_sort Askoxylakis, Vasileios
collection PubMed
description BACKGROUND: Radiotherapy, preferably combined with chemotherapy, is the treatment standard for locally advanced, unresectable non-small cell lung cancer (NSCLC). The tumor response to different therapy protocols is variable, with hypoxia known to be a major factor that negatively influences treatment effectiveness. Visualisation of tumor hypoxia prior to the use of modern radiation therapy strategies, such as intensity modulated radiation therapy (IMRT), might allow optimized dose applications to the target volume, leading to improvement of therapy outcome. (18) F-fluoromisonidazole dynamic positron emission tomography and computed tomography ((18) F-FMISO dPET-CT) and functional magnetic resonance imaging (functional MRI) are attractive options for imaging tumor hypoxia. METHODS/DESIGN: The HIL trial is a single centre study combining multimodal hypoxia imaging with (18) F-FMISO dPET-CT and functional MRI, with intensity modulated radiation therapy (IMRT) in patients with inoperable stage III NSCLC. 15 patients will be recruited in the study. All patients undergo initial FDG PET-CT and serial (18) F-FMISO dPET-CT and functional MRI before treatment, at week 5 of radiotherapy and 6 weeks post treatment. Radiation therapy is performed as inversely planned IMRT based on 4D-CT. DISCUSSION: Primary objectives of the trial are to characterize the correlation of (18) F-FMISO dPET-CT and functional MRI for tumor hypoxia imaging in NSCLC and evaluate possible effects of radiation therapy on tumor re-oxygenation. Further objectives include the generation of data regarding the prognostic value of (18) F-FMISO dPET-CT and functional MRI for locoregional control, progression free survival and overall survival of NSCLC treated with IMRT, which will form the basis for larger clinical trials focusing on possible interactions between tumor oxygenation and radiotherapy outcome. TRIAL REGISTRATION: The ClinicalTrials.gov protocol ID is NCT01617980
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spelling pubmed-35036482012-11-22 Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial Askoxylakis, Vasileios Dinkel, Julien Eichinger, Monika Stieltjes, Bram Sommer, Gregor Strauss, Ludwig G Dimitrakopoulou-Strauss, Antonia Kopp-Schneider, Annette Haberkorn, Uwe Huber, Peter E Bischof, Marc Debus, Jürgen Thieke, Christian Radiat Oncol Study Protocol BACKGROUND: Radiotherapy, preferably combined with chemotherapy, is the treatment standard for locally advanced, unresectable non-small cell lung cancer (NSCLC). The tumor response to different therapy protocols is variable, with hypoxia known to be a major factor that negatively influences treatment effectiveness. Visualisation of tumor hypoxia prior to the use of modern radiation therapy strategies, such as intensity modulated radiation therapy (IMRT), might allow optimized dose applications to the target volume, leading to improvement of therapy outcome. (18) F-fluoromisonidazole dynamic positron emission tomography and computed tomography ((18) F-FMISO dPET-CT) and functional magnetic resonance imaging (functional MRI) are attractive options for imaging tumor hypoxia. METHODS/DESIGN: The HIL trial is a single centre study combining multimodal hypoxia imaging with (18) F-FMISO dPET-CT and functional MRI, with intensity modulated radiation therapy (IMRT) in patients with inoperable stage III NSCLC. 15 patients will be recruited in the study. All patients undergo initial FDG PET-CT and serial (18) F-FMISO dPET-CT and functional MRI before treatment, at week 5 of radiotherapy and 6 weeks post treatment. Radiation therapy is performed as inversely planned IMRT based on 4D-CT. DISCUSSION: Primary objectives of the trial are to characterize the correlation of (18) F-FMISO dPET-CT and functional MRI for tumor hypoxia imaging in NSCLC and evaluate possible effects of radiation therapy on tumor re-oxygenation. Further objectives include the generation of data regarding the prognostic value of (18) F-FMISO dPET-CT and functional MRI for locoregional control, progression free survival and overall survival of NSCLC treated with IMRT, which will form the basis for larger clinical trials focusing on possible interactions between tumor oxygenation and radiotherapy outcome. TRIAL REGISTRATION: The ClinicalTrials.gov protocol ID is NCT01617980 BioMed Central 2012-09-14 /pmc/articles/PMC3503648/ /pubmed/22974533 http://dx.doi.org/10.1186/1748-717X-7-157 Text en Copyright ©2012 Askoxylakis et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Study Protocol
Askoxylakis, Vasileios
Dinkel, Julien
Eichinger, Monika
Stieltjes, Bram
Sommer, Gregor
Strauss, Ludwig G
Dimitrakopoulou-Strauss, Antonia
Kopp-Schneider, Annette
Haberkorn, Uwe
Huber, Peter E
Bischof, Marc
Debus, Jürgen
Thieke, Christian
Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial
title Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial
title_full Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial
title_fullStr Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial
title_full_unstemmed Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial
title_short Multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the HIL trial
title_sort multimodal hypoxia imaging and intensity modulated radiation therapy for unresectable non-small-cell lung cancer: the hil trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503648/
https://www.ncbi.nlm.nih.gov/pubmed/22974533
http://dx.doi.org/10.1186/1748-717X-7-157
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