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Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma
SIMPLE SUMMARY: In this study, we evaluated the association of immune mediated thyroid dysfunction (irT) with survival in 123 metastatic renal cell carcinoma patients treated with immunotherapy in a single center. We found that irT is a prevalent and early event associated with prolonged survival in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870210/ https://www.ncbi.nlm.nih.gov/pubmed/35205622 http://dx.doi.org/10.3390/cancers14040875 |
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author | Sagie, Shira Gadot, Moran Levartovsky, Meital Gantz Sorotsky, Hadas Berger, Raanan Sarfaty, Michal Percik, Ruth |
author_facet | Sagie, Shira Gadot, Moran Levartovsky, Meital Gantz Sorotsky, Hadas Berger, Raanan Sarfaty, Michal Percik, Ruth |
author_sort | Sagie, Shira |
collection | PubMed |
description | SIMPLE SUMMARY: In this study, we evaluated the association of immune mediated thyroid dysfunction (irT) with survival in 123 metastatic renal cell carcinoma patients treated with immunotherapy in a single center. We found that irT is a prevalent and early event associated with prolonged survival in high-risk patients. ABSTRACT: Immune checkpoint inhibitors (CPI) are indicated for metastatic renal cell carcinoma (mRCC). Immune-related thyroiditis (irT), an immune-related adverse event (irAE), affects up to 30% of patients. We aimed to determine whether irT is associated with overall survival in mRCC. A retrospective cohort study of 123 consecutive patients treated with CPI for mRCC in a single center between 2015 and 2020 was conducted. Disease risk stratification was assessed by two methods: Heng criteria and a novel dichotomic stratification system to “Low risk” versus “High risk” adding number of metastatic sites. Thirty-eight percent of patients developed irT. In the general cohort, irT was not associated with a survival benefit. However, irT was associated with better survival in the poor risk group per Heng criteria (n = 17, HR = 0.25, p = 0.04) and in the novel “High risk” group (HR = 0.28, n = 42, p = 0.01), including after accounting for covariates in multivariate analysis (HR = 0.27, p = 0.003). Having any irAE was associated with improved survival in the whole cohort, with no significant correlation of any specific irAE, in either the whole cohort or the “High risk” group. We conclude that irT is an early and prevalent irAE, associated with prolonged survival in patients with poor/“High” risk mRCC. |
format | Online Article Text |
id | pubmed-8870210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88702102022-02-25 Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma Sagie, Shira Gadot, Moran Levartovsky, Meital Gantz Sorotsky, Hadas Berger, Raanan Sarfaty, Michal Percik, Ruth Cancers (Basel) Article SIMPLE SUMMARY: In this study, we evaluated the association of immune mediated thyroid dysfunction (irT) with survival in 123 metastatic renal cell carcinoma patients treated with immunotherapy in a single center. We found that irT is a prevalent and early event associated with prolonged survival in high-risk patients. ABSTRACT: Immune checkpoint inhibitors (CPI) are indicated for metastatic renal cell carcinoma (mRCC). Immune-related thyroiditis (irT), an immune-related adverse event (irAE), affects up to 30% of patients. We aimed to determine whether irT is associated with overall survival in mRCC. A retrospective cohort study of 123 consecutive patients treated with CPI for mRCC in a single center between 2015 and 2020 was conducted. Disease risk stratification was assessed by two methods: Heng criteria and a novel dichotomic stratification system to “Low risk” versus “High risk” adding number of metastatic sites. Thirty-eight percent of patients developed irT. In the general cohort, irT was not associated with a survival benefit. However, irT was associated with better survival in the poor risk group per Heng criteria (n = 17, HR = 0.25, p = 0.04) and in the novel “High risk” group (HR = 0.28, n = 42, p = 0.01), including after accounting for covariates in multivariate analysis (HR = 0.27, p = 0.003). Having any irAE was associated with improved survival in the whole cohort, with no significant correlation of any specific irAE, in either the whole cohort or the “High risk” group. We conclude that irT is an early and prevalent irAE, associated with prolonged survival in patients with poor/“High” risk mRCC. MDPI 2022-02-10 /pmc/articles/PMC8870210/ /pubmed/35205622 http://dx.doi.org/10.3390/cancers14040875 Text en © 2022 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 | Article Sagie, Shira Gadot, Moran Levartovsky, Meital Gantz Sorotsky, Hadas Berger, Raanan Sarfaty, Michal Percik, Ruth Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma |
title | Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma |
title_full | Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma |
title_fullStr | Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma |
title_full_unstemmed | Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma |
title_short | Immune-Related Thyroiditis as a Predictor for Survival in Metastatic Renal Cell Carcinoma |
title_sort | immune-related thyroiditis as a predictor for survival in metastatic renal cell carcinoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870210/ https://www.ncbi.nlm.nih.gov/pubmed/35205622 http://dx.doi.org/10.3390/cancers14040875 |
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