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Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy

Nivolumab plus ipilimumab combined therapy is one of the promising drugs that enhance the anti- immune response in patients with advanced melanoma. Therefore, to increase its response rate is of great interest to dermatologists. Recent reports suggested that, since CD8+ T cells after the administrat...

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Autores principales: Yoshida, Saaya, Fujimura, Taku, Kambayashi, Yumi, Amagai, Ryo, Hashimoto, Akira, Aiba, Setsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872996/
https://www.ncbi.nlm.nih.gov/pubmed/31762756
http://dx.doi.org/10.1159/000504019
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author Yoshida, Saaya
Fujimura, Taku
Kambayashi, Yumi
Amagai, Ryo
Hashimoto, Akira
Aiba, Setsuya
author_facet Yoshida, Saaya
Fujimura, Taku
Kambayashi, Yumi
Amagai, Ryo
Hashimoto, Akira
Aiba, Setsuya
author_sort Yoshida, Saaya
collection PubMed
description Nivolumab plus ipilimumab combined therapy is one of the promising drugs that enhance the anti- immune response in patients with advanced melanoma. Therefore, to increase its response rate is of great interest to dermatologists. Recent reports suggested that, since CD8+ T cells after the administration of ICIs increase the RANKL expression to induce an immunosuppressive tumor microenvironment in melanoma, denosumab might enhance the anti-tumor effects of immune checkpoint inhibitors, such as nivolumab and ipilimumab. In this report, we present a case of multiple metastatic melanoma with nivolumab, ipilimumab plus denosumab combined therapy.
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spelling pubmed-68729962019-11-22 Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy Yoshida, Saaya Fujimura, Taku Kambayashi, Yumi Amagai, Ryo Hashimoto, Akira Aiba, Setsuya Case Rep Oncol Case Report Nivolumab plus ipilimumab combined therapy is one of the promising drugs that enhance the anti- immune response in patients with advanced melanoma. Therefore, to increase its response rate is of great interest to dermatologists. Recent reports suggested that, since CD8+ T cells after the administration of ICIs increase the RANKL expression to induce an immunosuppressive tumor microenvironment in melanoma, denosumab might enhance the anti-tumor effects of immune checkpoint inhibitors, such as nivolumab and ipilimumab. In this report, we present a case of multiple metastatic melanoma with nivolumab, ipilimumab plus denosumab combined therapy. S. Karger AG 2019-10-30 /pmc/articles/PMC6872996/ /pubmed/31762756 http://dx.doi.org/10.1159/000504019 Text en Copyright © 2019 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Yoshida, Saaya
Fujimura, Taku
Kambayashi, Yumi
Amagai, Ryo
Hashimoto, Akira
Aiba, Setsuya
Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy
title Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy
title_full Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy
title_fullStr Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy
title_full_unstemmed Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy
title_short Successful Treatment of Multiple Metastatic Melanoma with Nivolumab, Ipilimumab plus Denosumab Combined Therapy
title_sort successful treatment of multiple metastatic melanoma with nivolumab, ipilimumab plus denosumab combined therapy
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6872996/
https://www.ncbi.nlm.nih.gov/pubmed/31762756
http://dx.doi.org/10.1159/000504019
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