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ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies

BACKGROUND: Radiotherapy is one of the cornerstones of the treatment of Head and Neck Squamous Cell Carcinomas (HNSCC). However, radioresistance is associated with a high risk of recurrence. To propose strategies (such as combinations with drugs) that could over intrinsic radioresistance, it is cruc...

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Autores principales: Perréard, Marion, Florent, Romane, Divoux, Jordane, Grellard, Jean-Michel, Lequesne, Justine, Briand, Mélanie, Clarisse, Bénédicte, Rousseau, Nathalie, Lebreton, Esther, Dubois, Brice, Harter, Valentin, Lasne-Cardon, Audrey, Drouet, Julien, Johnson, Alisson, Le Page, Anne-Laure, Bazille, Céline, Jeanne, Corinne, Figeac, Martin, Goardon, Nicolas, Vaur, Dominique, Micault, Emmanuel, Humbert, Maxime, Thariat, Juliette, Babin, Emmanuel, Poulain, Laurent, Weiswald, Louis-Bastien, Bastit, Vianney
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999487/
https://www.ncbi.nlm.nih.gov/pubmed/36894916
http://dx.doi.org/10.1186/s12885-023-10692-x
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author Perréard, Marion
Florent, Romane
Divoux, Jordane
Grellard, Jean-Michel
Lequesne, Justine
Briand, Mélanie
Clarisse, Bénédicte
Rousseau, Nathalie
Lebreton, Esther
Dubois, Brice
Harter, Valentin
Lasne-Cardon, Audrey
Drouet, Julien
Johnson, Alisson
Le Page, Anne-Laure
Bazille, Céline
Jeanne, Corinne
Figeac, Martin
Goardon, Nicolas
Vaur, Dominique
Micault, Emmanuel
Humbert, Maxime
Thariat, Juliette
Babin, Emmanuel
Poulain, Laurent
Weiswald, Louis-Bastien
Bastit, Vianney
author_facet Perréard, Marion
Florent, Romane
Divoux, Jordane
Grellard, Jean-Michel
Lequesne, Justine
Briand, Mélanie
Clarisse, Bénédicte
Rousseau, Nathalie
Lebreton, Esther
Dubois, Brice
Harter, Valentin
Lasne-Cardon, Audrey
Drouet, Julien
Johnson, Alisson
Le Page, Anne-Laure
Bazille, Céline
Jeanne, Corinne
Figeac, Martin
Goardon, Nicolas
Vaur, Dominique
Micault, Emmanuel
Humbert, Maxime
Thariat, Juliette
Babin, Emmanuel
Poulain, Laurent
Weiswald, Louis-Bastien
Bastit, Vianney
author_sort Perréard, Marion
collection PubMed
description BACKGROUND: Radiotherapy is one of the cornerstones of the treatment of Head and Neck Squamous Cell Carcinomas (HNSCC). However, radioresistance is associated with a high risk of recurrence. To propose strategies (such as combinations with drugs) that could over intrinsic radioresistance, it is crucial to predict the response to treatment. Patient-Derived Tumor Organoids (PDTO) are in vitro tridimensional microtumors obtained from patient’ own cancer samples. They have been shown to serve as reliable surrogates of the tumor response in patients. METHODS: The ORGAVADS study is a multicenter observational trial conducted to investigate the feasibility of generating and testing PDTO derived from HNSCC for the evaluation of sensitivity to treatments. PDTO are obtained after dissociation of resected tumors remaining from tissues necessary for the diagnosis. Embedding of tumor cells is then performed in extracellular matrix and culture in medium supplemented with growth factors and inhibitors. Histological and immunohistochemical characterizations are performed to validate the resemblance between PDTO and their original tumor. Response of PDTO to chemotherapy, radiotherapy and innovating combinations are assessed, as well as response to immunotherapy using co-cultures of PDTO with autologous immune cells collected from patient blood samples. Transcriptomic and genetic analyses of PDTO allow validation of the models compared to patients’ own tumor and identification of potential predictive biomarkers. DISCUSSION: This study is designed to develop PDTO models from HNSCC. It will allow comparing the response of PDTO to treatment and the clinical response of the patients from whom they are derived. Our aim is to study the PDTO ability to predict the clinical response to treatment for each patient in view of a personalized medicine as well as to establish a collection of HNSCC models that will be useful for future innovative strategies evaluation. TRIAL REGISTRATION: NCT04261192, registered February 7, 2020, last amendment v4 accepted on June, 2021.
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spelling pubmed-99994872023-03-11 ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies Perréard, Marion Florent, Romane Divoux, Jordane Grellard, Jean-Michel Lequesne, Justine Briand, Mélanie Clarisse, Bénédicte Rousseau, Nathalie Lebreton, Esther Dubois, Brice Harter, Valentin Lasne-Cardon, Audrey Drouet, Julien Johnson, Alisson Le Page, Anne-Laure Bazille, Céline Jeanne, Corinne Figeac, Martin Goardon, Nicolas Vaur, Dominique Micault, Emmanuel Humbert, Maxime Thariat, Juliette Babin, Emmanuel Poulain, Laurent Weiswald, Louis-Bastien Bastit, Vianney BMC Cancer Study Protocol BACKGROUND: Radiotherapy is one of the cornerstones of the treatment of Head and Neck Squamous Cell Carcinomas (HNSCC). However, radioresistance is associated with a high risk of recurrence. To propose strategies (such as combinations with drugs) that could over intrinsic radioresistance, it is crucial to predict the response to treatment. Patient-Derived Tumor Organoids (PDTO) are in vitro tridimensional microtumors obtained from patient’ own cancer samples. They have been shown to serve as reliable surrogates of the tumor response in patients. METHODS: The ORGAVADS study is a multicenter observational trial conducted to investigate the feasibility of generating and testing PDTO derived from HNSCC for the evaluation of sensitivity to treatments. PDTO are obtained after dissociation of resected tumors remaining from tissues necessary for the diagnosis. Embedding of tumor cells is then performed in extracellular matrix and culture in medium supplemented with growth factors and inhibitors. Histological and immunohistochemical characterizations are performed to validate the resemblance between PDTO and their original tumor. Response of PDTO to chemotherapy, radiotherapy and innovating combinations are assessed, as well as response to immunotherapy using co-cultures of PDTO with autologous immune cells collected from patient blood samples. Transcriptomic and genetic analyses of PDTO allow validation of the models compared to patients’ own tumor and identification of potential predictive biomarkers. DISCUSSION: This study is designed to develop PDTO models from HNSCC. It will allow comparing the response of PDTO to treatment and the clinical response of the patients from whom they are derived. Our aim is to study the PDTO ability to predict the clinical response to treatment for each patient in view of a personalized medicine as well as to establish a collection of HNSCC models that will be useful for future innovative strategies evaluation. TRIAL REGISTRATION: NCT04261192, registered February 7, 2020, last amendment v4 accepted on June, 2021. BioMed Central 2023-03-09 /pmc/articles/PMC9999487/ /pubmed/36894916 http://dx.doi.org/10.1186/s12885-023-10692-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Perréard, Marion
Florent, Romane
Divoux, Jordane
Grellard, Jean-Michel
Lequesne, Justine
Briand, Mélanie
Clarisse, Bénédicte
Rousseau, Nathalie
Lebreton, Esther
Dubois, Brice
Harter, Valentin
Lasne-Cardon, Audrey
Drouet, Julien
Johnson, Alisson
Le Page, Anne-Laure
Bazille, Céline
Jeanne, Corinne
Figeac, Martin
Goardon, Nicolas
Vaur, Dominique
Micault, Emmanuel
Humbert, Maxime
Thariat, Juliette
Babin, Emmanuel
Poulain, Laurent
Weiswald, Louis-Bastien
Bastit, Vianney
ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
title ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
title_full ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
title_fullStr ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
title_full_unstemmed ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
title_short ORGAVADS: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
title_sort orgavads: establishment of tumor organoids from head and neck squamous cell carcinoma to assess their response to innovative therapies
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999487/
https://www.ncbi.nlm.nih.gov/pubmed/36894916
http://dx.doi.org/10.1186/s12885-023-10692-x
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