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Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma

Retinoblastoma is the most common pediatric eye cancer. It is currently treated with a limited number of drugs, adapted from other pediatric cancer treatments. Drug toxicity and relapse of the disease warrant new therapeutic strategies for these young patients. In this study, we developed a robust t...

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Autores principales: Sinenko, Irina L., Kuttler, Fabien, Simeonov, Valentin, Moulin, Alexandre, Aouad, Patrick, Stathopoulos, Christina, Munier, Francis L., Berger, Adeline, Dyson, Paul J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475790/
https://www.ncbi.nlm.nih.gov/pubmed/37340597
http://dx.doi.org/10.1111/cas.15878
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author Sinenko, Irina L.
Kuttler, Fabien
Simeonov, Valentin
Moulin, Alexandre
Aouad, Patrick
Stathopoulos, Christina
Munier, Francis L.
Berger, Adeline
Dyson, Paul J.
author_facet Sinenko, Irina L.
Kuttler, Fabien
Simeonov, Valentin
Moulin, Alexandre
Aouad, Patrick
Stathopoulos, Christina
Munier, Francis L.
Berger, Adeline
Dyson, Paul J.
author_sort Sinenko, Irina L.
collection PubMed
description Retinoblastoma is the most common pediatric eye cancer. It is currently treated with a limited number of drugs, adapted from other pediatric cancer treatments. Drug toxicity and relapse of the disease warrant new therapeutic strategies for these young patients. In this study, we developed a robust tumoroid‐based platform to test chemotherapeutic agents in combination with focal therapy (thermotherapy) – a treatment option widely used in clinical practice – in accordance with clinically relevant trial protocols. The model consists of matrix‐embedded tumoroids that retain retinoblastoma features and respond to repeated chemotherapeutic drug exposure similarly to advanced clinical cases. Moreover, the screening platform includes a diode laser (810 nm, 0.3 W) to selectively heat the tumoroids, combined with an on‐line system to monitor the intratumoral and surrounding temperatures. This allows the reproduction of the clinical settings of thermotherapy and combined chemothermotherapy treatments. When testing the two main drugs currently used in clinics to treat retinoblastoma in our model, we observed results similar to those clinically obtained, validating the utility of the model. This screening platform is the first system to accurately reproduce clinically relevant treatment methods and should lead to the identification of more efficient drugs to treat retinoblastoma.
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spelling pubmed-104757902023-09-05 Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma Sinenko, Irina L. Kuttler, Fabien Simeonov, Valentin Moulin, Alexandre Aouad, Patrick Stathopoulos, Christina Munier, Francis L. Berger, Adeline Dyson, Paul J. Cancer Sci ORIGINAL ARTICLES Retinoblastoma is the most common pediatric eye cancer. It is currently treated with a limited number of drugs, adapted from other pediatric cancer treatments. Drug toxicity and relapse of the disease warrant new therapeutic strategies for these young patients. In this study, we developed a robust tumoroid‐based platform to test chemotherapeutic agents in combination with focal therapy (thermotherapy) – a treatment option widely used in clinical practice – in accordance with clinically relevant trial protocols. The model consists of matrix‐embedded tumoroids that retain retinoblastoma features and respond to repeated chemotherapeutic drug exposure similarly to advanced clinical cases. Moreover, the screening platform includes a diode laser (810 nm, 0.3 W) to selectively heat the tumoroids, combined with an on‐line system to monitor the intratumoral and surrounding temperatures. This allows the reproduction of the clinical settings of thermotherapy and combined chemothermotherapy treatments. When testing the two main drugs currently used in clinics to treat retinoblastoma in our model, we observed results similar to those clinically obtained, validating the utility of the model. This screening platform is the first system to accurately reproduce clinically relevant treatment methods and should lead to the identification of more efficient drugs to treat retinoblastoma. John Wiley and Sons Inc. 2023-06-20 /pmc/articles/PMC10475790/ /pubmed/37340597 http://dx.doi.org/10.1111/cas.15878 Text en © 2023 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle ORIGINAL ARTICLES
Sinenko, Irina L.
Kuttler, Fabien
Simeonov, Valentin
Moulin, Alexandre
Aouad, Patrick
Stathopoulos, Christina
Munier, Francis L.
Berger, Adeline
Dyson, Paul J.
Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
title Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
title_full Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
title_fullStr Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
title_full_unstemmed Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
title_short Translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
title_sort translational screening platform to evaluate chemotherapy in combination with focal therapy for retinoblastoma
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475790/
https://www.ncbi.nlm.nih.gov/pubmed/37340597
http://dx.doi.org/10.1111/cas.15878
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