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Checkpointinhibitoren in der Tumortherapie
In recent years, a breakthrough in tumor therapy was achieved with the development of checkpoint inhibitors. Checkpoint inhibitors activate the immune defense against tumors by overcoming the inhibitory effect of specific cell surface proteins acting as control points, the so-called checkpoints. Thi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648013/ https://www.ncbi.nlm.nih.gov/pubmed/33001218 http://dx.doi.org/10.1007/s00103-020-03221-9 |
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author | Zander, Hilke Müller-Egert, Susanne Zwiewka, Michal Groß, Steffen van Zandbergen, Ger Engelbergs, Jörg |
author_facet | Zander, Hilke Müller-Egert, Susanne Zwiewka, Michal Groß, Steffen van Zandbergen, Ger Engelbergs, Jörg |
author_sort | Zander, Hilke |
collection | PubMed |
description | In recent years, a breakthrough in tumor therapy was achieved with the development of checkpoint inhibitors. Checkpoint inhibitors activate the immune defense against tumors by overcoming the inhibitory effect of specific cell surface proteins acting as control points, the so-called checkpoints. This article provides an overview of the mode of action of approved checkpoint inhibitors and the status of current clinical development. The previously approved checkpoint inhibitors, monoclonal antibodies directed against the checkpoints CTLA‑4 and PD-1/PD-L1, are used in various tumor entities (including lung, kidney, and urothelial carcinoma; head and neck cancer; melanoma; and Hodgkin lymphoma). For the first time, long-term survival has been achieved in some of these patients with advanced tumors. Unfortunately, this efficacy can be observed only in a small proportion of the treated patients, depending on the tumor indication. Improved efficacy is envisioned by patient selection via predictive biomarkers and the development of combination therapies. Mandatory testing of the expression level of the predictive PD-L1 biomarker is already required in some indications to select patients with an enhanced benefit/risk relationship. |
format | Online Article Text |
id | pubmed-7648013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-76480132020-11-10 Checkpointinhibitoren in der Tumortherapie Zander, Hilke Müller-Egert, Susanne Zwiewka, Michal Groß, Steffen van Zandbergen, Ger Engelbergs, Jörg Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz Leitthema In recent years, a breakthrough in tumor therapy was achieved with the development of checkpoint inhibitors. Checkpoint inhibitors activate the immune defense against tumors by overcoming the inhibitory effect of specific cell surface proteins acting as control points, the so-called checkpoints. This article provides an overview of the mode of action of approved checkpoint inhibitors and the status of current clinical development. The previously approved checkpoint inhibitors, monoclonal antibodies directed against the checkpoints CTLA‑4 and PD-1/PD-L1, are used in various tumor entities (including lung, kidney, and urothelial carcinoma; head and neck cancer; melanoma; and Hodgkin lymphoma). For the first time, long-term survival has been achieved in some of these patients with advanced tumors. Unfortunately, this efficacy can be observed only in a small proportion of the treated patients, depending on the tumor indication. Improved efficacy is envisioned by patient selection via predictive biomarkers and the development of combination therapies. Mandatory testing of the expression level of the predictive PD-L1 biomarker is already required in some indications to select patients with an enhanced benefit/risk relationship. Springer Berlin Heidelberg 2020-10-01 2020 /pmc/articles/PMC7648013/ /pubmed/33001218 http://dx.doi.org/10.1007/s00103-020-03221-9 Text en © The Author(s) 2020 Open Access. Dieser Artikel wird unter der Creative Commons Namensnennung 4.0 International Lizenz veröffentlicht, welche die Nutzung, Vervielfältigung, Bearbeitung, Verbreitung und Wiedergabe in jeglichem Medium und Format erlaubt, sofern Sie den/die ursprünglichen Autor(en) und die Quelle ordnungsgemäß nennen, einen Link zur Creative Commons Lizenz beifügen und angeben, ob Änderungen vorgenommen wurden. Die in diesem Artikel enthaltenen Bilder und sonstiges Drittmaterial unterliegen ebenfalls der genannten Creative Commons Lizenz, sofern sich aus der Abbildungslegende nichts anderes ergibt. Sofern das betreffende Material nicht unter der genannten Creative Commons Lizenz steht und die betreffende Handlung nicht nach gesetzlichen Vorschriften erlaubt ist, ist für die oben aufgeführten Weiterverwendungen des Materials die Einwilligung des jeweiligen Rechteinhabers einzuholen. Weitere Details zur Lizenz entnehmen Sie bitte der Lizenzinformation auf http://creativecommons.org/licenses/by/4.0/deed.de. |
spellingShingle | Leitthema Zander, Hilke Müller-Egert, Susanne Zwiewka, Michal Groß, Steffen van Zandbergen, Ger Engelbergs, Jörg Checkpointinhibitoren in der Tumortherapie |
title | Checkpointinhibitoren in der Tumortherapie |
title_full | Checkpointinhibitoren in der Tumortherapie |
title_fullStr | Checkpointinhibitoren in der Tumortherapie |
title_full_unstemmed | Checkpointinhibitoren in der Tumortherapie |
title_short | Checkpointinhibitoren in der Tumortherapie |
title_sort | checkpointinhibitoren in der tumortherapie |
topic | Leitthema |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648013/ https://www.ncbi.nlm.nih.gov/pubmed/33001218 http://dx.doi.org/10.1007/s00103-020-03221-9 |
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