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Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab
Nivolumab and ipilimumab (NIVO + IPI) is standard therapy for patients with advanced renal cell carcinoma (RCC). Absolute lymphocyte count (ALC) is a valuable prognostic factor in patients with various cancers treated with immune checkpoint inhibitors. Herein, we determined the prognostic value of p...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053370/ https://www.ncbi.nlm.nih.gov/pubmed/36983417 http://dx.doi.org/10.3390/jcm12062417 |
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author | Ueda, Kosuke Ogasawara, Naoyuki Ito, Naoki Ohnishi, Satoshi Suekane, Hiroki Kurose, Hirofumi Hiroshige, Tasuku Chikui, Katsuaki Uemura, Keiichiro Nishihara, Kiyoaki Nakiri, Makoto Suekane, Shigetaka Igawa, Tsukasa |
author_facet | Ueda, Kosuke Ogasawara, Naoyuki Ito, Naoki Ohnishi, Satoshi Suekane, Hiroki Kurose, Hirofumi Hiroshige, Tasuku Chikui, Katsuaki Uemura, Keiichiro Nishihara, Kiyoaki Nakiri, Makoto Suekane, Shigetaka Igawa, Tsukasa |
author_sort | Ueda, Kosuke |
collection | PubMed |
description | Nivolumab and ipilimumab (NIVO + IPI) is standard therapy for patients with advanced renal cell carcinoma (RCC). Absolute lymphocyte count (ALC) is a valuable prognostic factor in patients with various cancers treated with immune checkpoint inhibitors. Herein, we determined the prognostic value of pretreatment ALC in advanced RCC patients treated with NIVO + IPI as first-line therapy. Data from 46 advanced RCC patients treated with NIVO + IPI between September 2018 and August 2022 were retrospectively reviewed and analyzed. Median progression-free survival (PFS) and overall survival (OS) were significantly shorter in patients with low than high ALC (PFS: p = 0.0095; OS: p = 0.0182). Multivariate analysis suggested that prior nephrectomy [hazard ratio (HR) = 3.854, 95% confidence interval (CI) = 1.433–10.359, p = 0.0075] and pretreatment ALC (HR = 2.513, 95% CI = 1.119–5.648, p = 0.0257) were independent factors for PFS. Our new prognostic ALNx model based on ALC and prior nephrectomy suggested that the poor-risk group was a predictor of significantly worse PFS (p < 0.0001) and OS (p = 0.0016). Collectively, the developed ALNx model may be a novel predictor of response in advanced RCC patients treated with NIVO + IPI. |
format | Online Article Text |
id | pubmed-10053370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100533702023-03-30 Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab Ueda, Kosuke Ogasawara, Naoyuki Ito, Naoki Ohnishi, Satoshi Suekane, Hiroki Kurose, Hirofumi Hiroshige, Tasuku Chikui, Katsuaki Uemura, Keiichiro Nishihara, Kiyoaki Nakiri, Makoto Suekane, Shigetaka Igawa, Tsukasa J Clin Med Article Nivolumab and ipilimumab (NIVO + IPI) is standard therapy for patients with advanced renal cell carcinoma (RCC). Absolute lymphocyte count (ALC) is a valuable prognostic factor in patients with various cancers treated with immune checkpoint inhibitors. Herein, we determined the prognostic value of pretreatment ALC in advanced RCC patients treated with NIVO + IPI as first-line therapy. Data from 46 advanced RCC patients treated with NIVO + IPI between September 2018 and August 2022 were retrospectively reviewed and analyzed. Median progression-free survival (PFS) and overall survival (OS) were significantly shorter in patients with low than high ALC (PFS: p = 0.0095; OS: p = 0.0182). Multivariate analysis suggested that prior nephrectomy [hazard ratio (HR) = 3.854, 95% confidence interval (CI) = 1.433–10.359, p = 0.0075] and pretreatment ALC (HR = 2.513, 95% CI = 1.119–5.648, p = 0.0257) were independent factors for PFS. Our new prognostic ALNx model based on ALC and prior nephrectomy suggested that the poor-risk group was a predictor of significantly worse PFS (p < 0.0001) and OS (p = 0.0016). Collectively, the developed ALNx model may be a novel predictor of response in advanced RCC patients treated with NIVO + IPI. MDPI 2023-03-21 /pmc/articles/PMC10053370/ /pubmed/36983417 http://dx.doi.org/10.3390/jcm12062417 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 | Article Ueda, Kosuke Ogasawara, Naoyuki Ito, Naoki Ohnishi, Satoshi Suekane, Hiroki Kurose, Hirofumi Hiroshige, Tasuku Chikui, Katsuaki Uemura, Keiichiro Nishihara, Kiyoaki Nakiri, Makoto Suekane, Shigetaka Igawa, Tsukasa Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab |
title | Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab |
title_full | Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab |
title_fullStr | Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab |
title_full_unstemmed | Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab |
title_short | Prognostic Value of Absolute Lymphocyte Count in Patients with Advanced Renal Cell Carcinoma Treated with Nivolumab plus Ipilimumab |
title_sort | prognostic value of absolute lymphocyte count in patients with advanced renal cell carcinoma treated with nivolumab plus ipilimumab |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053370/ https://www.ncbi.nlm.nih.gov/pubmed/36983417 http://dx.doi.org/10.3390/jcm12062417 |
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