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Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab
Nivolumab has shown good prognosis in renal cell carcinoma (RCC) patients previously treated with targeted therapy. We aimed to study irAE (immune-related adverse event) due to nivolumab and numbers of previous treatment lines in RCC patients. Between October 2016 and November 2019, 114 patients wer...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021322/ https://www.ncbi.nlm.nih.gov/pubmed/33787647 http://dx.doi.org/10.1097/MD.0000000000025402 |
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author | Mizutani, Kosuke Ito, Toshiki Takahara, Kiyoshi Ando, Ryosuke Ishihara, Takuma Yasui, Takahiro Shiroki, Ryoichi Miyake, Hideaki Koie, Takuya |
author_facet | Mizutani, Kosuke Ito, Toshiki Takahara, Kiyoshi Ando, Ryosuke Ishihara, Takuma Yasui, Takahiro Shiroki, Ryoichi Miyake, Hideaki Koie, Takuya |
author_sort | Mizutani, Kosuke |
collection | PubMed |
description | Nivolumab has shown good prognosis in renal cell carcinoma (RCC) patients previously treated with targeted therapy. We aimed to study irAE (immune-related adverse event) due to nivolumab and numbers of previous treatment lines in RCC patients. Between October 2016 and November 2019, 114 patients were treated with nivolumab as second- and later-line therapy. Among them, 110 patients with complete data were evaluated in this retrospective observational study. The primary endpoint was the relation between irAE and numbers of previous targeted therapies. Secondary endpoints were the relation of irAE with the duration of nivolumab treatment and with best overall response. For the primary analysis, proportional odds logistic regression was used to assess the effect of the number of prior therapies on the grade of any irAE as the ordinal variable. For the secondary analysis, binomial logistic regression models adjusted for the covariates were prepared to confirm the association between the incidence of irAE and the number of courses, number of nivolumab treatments and best overall response. Overall, 69, 66, 33, 13, 9 and 9 patients were treated with sunitinib, axitinib, pazopanib, sorafenib, temsirolimus and everolimus, respectively, prior to nivolumab. In total, 60 adverse events (Grade 1, 21; Grade 2, 21; Grade 3, 14; Grade 4, 2; not evaluated, 2) were identified in the patients treated with nivolumab. Ordered logistic regression analysis showed that the adjusted odds ratios of numbers of prior treatment for grade of irAE were 1.12 (numbers of prior treatment: 2 to 1) and 1.31 (3 to 1). Odds ratios of the numbers of nivolumab treatments and best overall response for the incidence of irAE were not significant. No statistically significant relations were found between grade of irAE and numbers of treatments prior to nivolumab. Patients treated with nivolumab should be closely monitored for irAE regardless number of previous therapies. |
format | Online Article Text |
id | pubmed-8021322 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-80213222021-04-07 Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab Mizutani, Kosuke Ito, Toshiki Takahara, Kiyoshi Ando, Ryosuke Ishihara, Takuma Yasui, Takahiro Shiroki, Ryoichi Miyake, Hideaki Koie, Takuya Medicine (Baltimore) 7300 Nivolumab has shown good prognosis in renal cell carcinoma (RCC) patients previously treated with targeted therapy. We aimed to study irAE (immune-related adverse event) due to nivolumab and numbers of previous treatment lines in RCC patients. Between October 2016 and November 2019, 114 patients were treated with nivolumab as second- and later-line therapy. Among them, 110 patients with complete data were evaluated in this retrospective observational study. The primary endpoint was the relation between irAE and numbers of previous targeted therapies. Secondary endpoints were the relation of irAE with the duration of nivolumab treatment and with best overall response. For the primary analysis, proportional odds logistic regression was used to assess the effect of the number of prior therapies on the grade of any irAE as the ordinal variable. For the secondary analysis, binomial logistic regression models adjusted for the covariates were prepared to confirm the association between the incidence of irAE and the number of courses, number of nivolumab treatments and best overall response. Overall, 69, 66, 33, 13, 9 and 9 patients were treated with sunitinib, axitinib, pazopanib, sorafenib, temsirolimus and everolimus, respectively, prior to nivolumab. In total, 60 adverse events (Grade 1, 21; Grade 2, 21; Grade 3, 14; Grade 4, 2; not evaluated, 2) were identified in the patients treated with nivolumab. Ordered logistic regression analysis showed that the adjusted odds ratios of numbers of prior treatment for grade of irAE were 1.12 (numbers of prior treatment: 2 to 1) and 1.31 (3 to 1). Odds ratios of the numbers of nivolumab treatments and best overall response for the incidence of irAE were not significant. No statistically significant relations were found between grade of irAE and numbers of treatments prior to nivolumab. Patients treated with nivolumab should be closely monitored for irAE regardless number of previous therapies. Lippincott Williams & Wilkins 2021-04-02 /pmc/articles/PMC8021322/ /pubmed/33787647 http://dx.doi.org/10.1097/MD.0000000000025402 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 7300 Mizutani, Kosuke Ito, Toshiki Takahara, Kiyoshi Ando, Ryosuke Ishihara, Takuma Yasui, Takahiro Shiroki, Ryoichi Miyake, Hideaki Koie, Takuya Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab |
title | Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab |
title_full | Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab |
title_fullStr | Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab |
title_full_unstemmed | Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab |
title_short | Frequency of pre-treatment may not increase the immune-related adverse events of RCC patients treated with nivolumab |
title_sort | frequency of pre-treatment may not increase the immune-related adverse events of rcc patients treated with nivolumab |
topic | 7300 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8021322/ https://www.ncbi.nlm.nih.gov/pubmed/33787647 http://dx.doi.org/10.1097/MD.0000000000025402 |
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