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Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report

The immune checkpoint inhibitor/tyrosine kinase inhibitor (ICI/TKI) combination treatment is currently the first-line treatment for metastatic renal cell carcinoma (mRCC). However, its efficacy beyond the third-line setting is expected to be relatively poor, and high-grade toxicities can develop by...

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Autores principales: Chang, Yueh-Shih, Chang, Pei-Hung, Wang, Deng-Huang, Chen, Chun-Bing, Huang, Chi-Ying F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419223/
https://www.ncbi.nlm.nih.gov/pubmed/37569525
http://dx.doi.org/10.3390/ijms241512149
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author Chang, Yueh-Shih
Chang, Pei-Hung
Wang, Deng-Huang
Chen, Chun-Bing
Huang, Chi-Ying F.
author_facet Chang, Yueh-Shih
Chang, Pei-Hung
Wang, Deng-Huang
Chen, Chun-Bing
Huang, Chi-Ying F.
author_sort Chang, Yueh-Shih
collection PubMed
description The immune checkpoint inhibitor/tyrosine kinase inhibitor (ICI/TKI) combination treatment is currently the first-line treatment for metastatic renal cell carcinoma (mRCC). However, its efficacy beyond the third-line setting is expected to be relatively poor, and high-grade toxicities can develop by prior exposure to multiple drugs, resulting in a relatively poor performance in patients. Determining the best treatment regimen and sequence remains difficult and requires further investigation in patients with mRCC. In this study, two cases of mRCC, who failed several lines of TKI and nivolumab but exhibited a good anticancer effect after rechallenging with axitinib, are described. Both patients had a faster time to best response and better progression-free survival (PFS) than during previous treatments. Moreover, the axitinib dose could be reduced to 2.5 mg daily when used in combination with nivolumab while continuing to exert an impressive anticancer effect. To determine the cytotoxic effect, we performed a lymphocyte activation test and found that the level of granzyme B released by cytotoxic T lymphocytes and natural killer cells was higher when axitinib was combined with nivolumab. To evaluate this result, a bioinformatics approach was used to analyze the PRISM database. In conclusion, based on the results of a lymphocyte activation test and PD-1 expression, our findings indicate that sequential therapy with axitinib rechallenge after nivolumab resistance is reasonable for the treatment of mRCC.
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spelling pubmed-104192232023-08-12 Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report Chang, Yueh-Shih Chang, Pei-Hung Wang, Deng-Huang Chen, Chun-Bing Huang, Chi-Ying F. Int J Mol Sci Case Report The immune checkpoint inhibitor/tyrosine kinase inhibitor (ICI/TKI) combination treatment is currently the first-line treatment for metastatic renal cell carcinoma (mRCC). However, its efficacy beyond the third-line setting is expected to be relatively poor, and high-grade toxicities can develop by prior exposure to multiple drugs, resulting in a relatively poor performance in patients. Determining the best treatment regimen and sequence remains difficult and requires further investigation in patients with mRCC. In this study, two cases of mRCC, who failed several lines of TKI and nivolumab but exhibited a good anticancer effect after rechallenging with axitinib, are described. Both patients had a faster time to best response and better progression-free survival (PFS) than during previous treatments. Moreover, the axitinib dose could be reduced to 2.5 mg daily when used in combination with nivolumab while continuing to exert an impressive anticancer effect. To determine the cytotoxic effect, we performed a lymphocyte activation test and found that the level of granzyme B released by cytotoxic T lymphocytes and natural killer cells was higher when axitinib was combined with nivolumab. To evaluate this result, a bioinformatics approach was used to analyze the PRISM database. In conclusion, based on the results of a lymphocyte activation test and PD-1 expression, our findings indicate that sequential therapy with axitinib rechallenge after nivolumab resistance is reasonable for the treatment of mRCC. MDPI 2023-07-29 /pmc/articles/PMC10419223/ /pubmed/37569525 http://dx.doi.org/10.3390/ijms241512149 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Case Report
Chang, Yueh-Shih
Chang, Pei-Hung
Wang, Deng-Huang
Chen, Chun-Bing
Huang, Chi-Ying F.
Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report
title Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report
title_full Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report
title_fullStr Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report
title_full_unstemmed Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report
title_short Axitinib Rechallenge Restores the Anticancer Effect after Nivolumab: A Case Report
title_sort axitinib rechallenge restores the anticancer effect after nivolumab: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10419223/
https://www.ncbi.nlm.nih.gov/pubmed/37569525
http://dx.doi.org/10.3390/ijms241512149
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