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Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma

INTRODUCTION: Hyperprogression, characterized by a rapid acceleration in tumor growth, is a novel pattern of progression recently described in patients treated with immune checkpoint inhibitors. This study aims to assess the incidence of hyperprogression in patients with advanced melanoma treated wi...

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Autores principales: Schuiveling, M., Tonk, E. H. J., Verheijden, R. J., Suijkerbuijk, K. P. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053186/
https://www.ncbi.nlm.nih.gov/pubmed/32929554
http://dx.doi.org/10.1007/s00262-020-02716-3
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author Schuiveling, M.
Tonk, E. H. J.
Verheijden, R. J.
Suijkerbuijk, K. P. M.
author_facet Schuiveling, M.
Tonk, E. H. J.
Verheijden, R. J.
Suijkerbuijk, K. P. M.
author_sort Schuiveling, M.
collection PubMed
description INTRODUCTION: Hyperprogression, characterized by a rapid acceleration in tumor growth, is a novel pattern of progression recently described in patients treated with immune checkpoint inhibitors. This study aims to assess the incidence of hyperprogression in patients with advanced melanoma treated with checkpoint inhibitors. METHODS: Clinical and radiological findings of all advanced melanoma patients who started checkpoint inhibitors between January 2013 and March 2019 in a tertiary academic center in the Netherlands were analyzed. Change in tumor burden was calculated by assessing volumetric tumor growth using the criteria as defined by immune Response Evaluation Criteria in Solid Tumors version 1.1. Hyperprogression was defined as a time to treatment failure less than 2 months with doubling of tumor burden and a twofold increase in tumor growth rate during treatment. Possible hyperprogression was defined as the presence of the first two criteria in the absence of a pre-baseline scan. RESULTS: Out of 206 treatment episodes in 168 patients, 75 were evaluable for hyperprogression and 87 for possible hyperprogression. Hyperprogression was observed in one patient (1.3%) and possible hyperprogression was observed in one patient (1.1%). CONCLUSION: Hyperprogression is rare in melanoma patients treated with immune checkpoint inhibitors. Our data question if hyperprogression really is a biological entity in metastatic melanoma.
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spelling pubmed-80531862021-05-05 Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma Schuiveling, M. Tonk, E. H. J. Verheijden, R. J. Suijkerbuijk, K. P. M. Cancer Immunol Immunother Research Report INTRODUCTION: Hyperprogression, characterized by a rapid acceleration in tumor growth, is a novel pattern of progression recently described in patients treated with immune checkpoint inhibitors. This study aims to assess the incidence of hyperprogression in patients with advanced melanoma treated with checkpoint inhibitors. METHODS: Clinical and radiological findings of all advanced melanoma patients who started checkpoint inhibitors between January 2013 and March 2019 in a tertiary academic center in the Netherlands were analyzed. Change in tumor burden was calculated by assessing volumetric tumor growth using the criteria as defined by immune Response Evaluation Criteria in Solid Tumors version 1.1. Hyperprogression was defined as a time to treatment failure less than 2 months with doubling of tumor burden and a twofold increase in tumor growth rate during treatment. Possible hyperprogression was defined as the presence of the first two criteria in the absence of a pre-baseline scan. RESULTS: Out of 206 treatment episodes in 168 patients, 75 were evaluable for hyperprogression and 87 for possible hyperprogression. Hyperprogression was observed in one patient (1.3%) and possible hyperprogression was observed in one patient (1.1%). CONCLUSION: Hyperprogression is rare in melanoma patients treated with immune checkpoint inhibitors. Our data question if hyperprogression really is a biological entity in metastatic melanoma. Springer Berlin Heidelberg 2020-09-14 2021 /pmc/articles/PMC8053186/ /pubmed/32929554 http://dx.doi.org/10.1007/s00262-020-02716-3 Text en © The Author(s) 2020 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
Schuiveling, M.
Tonk, E. H. J.
Verheijden, R. J.
Suijkerbuijk, K. P. M.
Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
title Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
title_full Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
title_fullStr Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
title_full_unstemmed Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
title_short Hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
title_sort hyperprogressive disease rarely occurs during checkpoint inhibitor treatment for advanced melanoma
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8053186/
https://www.ncbi.nlm.nih.gov/pubmed/32929554
http://dx.doi.org/10.1007/s00262-020-02716-3
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