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Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma

BACKGROUND: Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine cutaneous malignancy with poor prognosis. In Europe, approved systemic therapies are limited to the PD-L1 inhibitor avelumab. For avelumab-refractory patients, efficient and safe treatment options are lacking. METHODS: A...

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Autores principales: Glutsch, Valerie, Kneitz, Hermann, Gesierich, Anja, Goebeler, Matthias, Haferkamp, Sebastian, Becker, Jürgen C., Ugurel, Selma, Schilling, Bastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195807/
https://www.ncbi.nlm.nih.gov/pubmed/33439294
http://dx.doi.org/10.1007/s00262-020-02832-0
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author Glutsch, Valerie
Kneitz, Hermann
Gesierich, Anja
Goebeler, Matthias
Haferkamp, Sebastian
Becker, Jürgen C.
Ugurel, Selma
Schilling, Bastian
author_facet Glutsch, Valerie
Kneitz, Hermann
Gesierich, Anja
Goebeler, Matthias
Haferkamp, Sebastian
Becker, Jürgen C.
Ugurel, Selma
Schilling, Bastian
author_sort Glutsch, Valerie
collection PubMed
description BACKGROUND: Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine cutaneous malignancy with poor prognosis. In Europe, approved systemic therapies are limited to the PD-L1 inhibitor avelumab. For avelumab-refractory patients, efficient and safe treatment options are lacking. METHODS: At three different sites in Germany, clinical and molecular data of patients with metastatic MCC being refractory to the PD-L1 inhibitor avelumab and who were later on treated with combined IPI/NIVO were retrospectively collected and evaluated. RESULTS: Five patients treated at three different academic sites in Germany were enrolled. Three out of five patients investigated for this report responded to combined IPI/NIVO according to RECIST 1.1. Combined immunotherapy was well tolerated without any grade II or III immune-related adverse events. Two out of three responders to IPI/NIVO received platinum-based chemotherapy in between avelumab and combined immunotherapy. CONCLUSION: In this small retrospective study, we observed a high response rate and durable responses to subsequent combined immunotherapy with IPI/NIVO in avelumab-refractory metastatic MCC patients. In conclusion, our data suggest a promising activity of second- or third-line PD-1- plus CTLA-4-blockade in patients with anti-PD-L1-refractory MCC.
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spelling pubmed-81958072021-06-28 Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma Glutsch, Valerie Kneitz, Hermann Gesierich, Anja Goebeler, Matthias Haferkamp, Sebastian Becker, Jürgen C. Ugurel, Selma Schilling, Bastian Cancer Immunol Immunother Research Report BACKGROUND: Merkel cell carcinoma (MCC) is a rare and aggressive neuroendocrine cutaneous malignancy with poor prognosis. In Europe, approved systemic therapies are limited to the PD-L1 inhibitor avelumab. For avelumab-refractory patients, efficient and safe treatment options are lacking. METHODS: At three different sites in Germany, clinical and molecular data of patients with metastatic MCC being refractory to the PD-L1 inhibitor avelumab and who were later on treated with combined IPI/NIVO were retrospectively collected and evaluated. RESULTS: Five patients treated at three different academic sites in Germany were enrolled. Three out of five patients investigated for this report responded to combined IPI/NIVO according to RECIST 1.1. Combined immunotherapy was well tolerated without any grade II or III immune-related adverse events. Two out of three responders to IPI/NIVO received platinum-based chemotherapy in between avelumab and combined immunotherapy. CONCLUSION: In this small retrospective study, we observed a high response rate and durable responses to subsequent combined immunotherapy with IPI/NIVO in avelumab-refractory metastatic MCC patients. In conclusion, our data suggest a promising activity of second- or third-line PD-1- plus CTLA-4-blockade in patients with anti-PD-L1-refractory MCC. Springer Berlin Heidelberg 2021-01-13 2021 /pmc/articles/PMC8195807/ /pubmed/33439294 http://dx.doi.org/10.1007/s00262-020-02832-0 Text en © The Author(s) 2021 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/) .
spellingShingle Research Report
Glutsch, Valerie
Kneitz, Hermann
Gesierich, Anja
Goebeler, Matthias
Haferkamp, Sebastian
Becker, Jürgen C.
Ugurel, Selma
Schilling, Bastian
Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma
title Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma
title_full Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma
title_fullStr Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma
title_full_unstemmed Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma
title_short Activity of ipilimumab plus nivolumab in avelumab-refractory Merkel cell carcinoma
title_sort activity of ipilimumab plus nivolumab in avelumab-refractory merkel cell carcinoma
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8195807/
https://www.ncbi.nlm.nih.gov/pubmed/33439294
http://dx.doi.org/10.1007/s00262-020-02832-0
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