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Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death

In September 2020, the Japanese government approved cetuximab saratolacan (previously known as RM-1929, commercial name: Akalux) for the treatment of unresectable locally advanced or recurrent head and neck cancer. Cetuximab saratolacan is a chemical conjugate of the photosensitizer IR700 with cetux...

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Autores principales: Gomes-da-Silva, Lígia C., Kepp, Oliver, Kroemer, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595598/
https://www.ncbi.nlm.nih.gov/pubmed/33178498
http://dx.doi.org/10.1080/2162402X.2020.1841393
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author Gomes-da-Silva, Lígia C.
Kepp, Oliver
Kroemer, Guido
author_facet Gomes-da-Silva, Lígia C.
Kepp, Oliver
Kroemer, Guido
author_sort Gomes-da-Silva, Lígia C.
collection PubMed
description In September 2020, the Japanese government approved cetuximab saratolacan (previously known as RM-1929, commercial name: Akalux) for the treatment of unresectable locally advanced or recurrent head and neck cancer. Cetuximab saratolacan is a chemical conjugate of the photosensitizer IR700 with cetuximab, which targets EGFR. The treatment consists in the intravenous injection of cetuximab saratolacan, which binds to head and neck cancer cells expressing high levels of EGFR, followed by illumination of the tumor with red light (690 nm) for photodynamic therapy. This approach causes immunogenic cell death in malignant tissues, thus triggering a potent anticancer immune response.
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spelling pubmed-75955982020-11-10 Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death Gomes-da-Silva, Lígia C. Kepp, Oliver Kroemer, Guido Oncoimmunology Editorial In September 2020, the Japanese government approved cetuximab saratolacan (previously known as RM-1929, commercial name: Akalux) for the treatment of unresectable locally advanced or recurrent head and neck cancer. Cetuximab saratolacan is a chemical conjugate of the photosensitizer IR700 with cetuximab, which targets EGFR. The treatment consists in the intravenous injection of cetuximab saratolacan, which binds to head and neck cancer cells expressing high levels of EGFR, followed by illumination of the tumor with red light (690 nm) for photodynamic therapy. This approach causes immunogenic cell death in malignant tissues, thus triggering a potent anticancer immune response. Taylor & Francis 2020-10-27 /pmc/articles/PMC7595598/ /pubmed/33178498 http://dx.doi.org/10.1080/2162402X.2020.1841393 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Editorial
Gomes-da-Silva, Lígia C.
Kepp, Oliver
Kroemer, Guido
Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
title Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
title_full Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
title_fullStr Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
title_full_unstemmed Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
title_short Regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
title_sort regulatory approval of photoimmunotherapy: photodynamic therapy that induces immunogenic cell death
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595598/
https://www.ncbi.nlm.nih.gov/pubmed/33178498
http://dx.doi.org/10.1080/2162402X.2020.1841393
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