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Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma

BACKGROUND: Due to the significant heterogeneity of renal cell carcinoma (RCC), immune checkpoints may express differently between primary and metastatic tumor. We aimed to evaluate the differential expression of TIM-3 between the primary and metastatic sites of RCC. METHODS: Cases of RCC with metas...

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Autores principales: Zhang, Xingming, Yin, Xiaoxue, Zhang, Haoran, Sun, Guangxi, Yang, Yaojing, Chen, Junru, Shu, Kunpeng, Zhao, Jinge, Zhao, Peng, Chen, Ni, Wang, Jia, Shen, Pengfei, Zeng, Hao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329070/
https://www.ncbi.nlm.nih.gov/pubmed/30630458
http://dx.doi.org/10.1186/s12885-019-5273-5
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author Zhang, Xingming
Yin, Xiaoxue
Zhang, Haoran
Sun, Guangxi
Yang, Yaojing
Chen, Junru
Shu, Kunpeng
Zhao, Jinge
Zhao, Peng
Chen, Ni
Wang, Jia
Shen, Pengfei
Zeng, Hao
author_facet Zhang, Xingming
Yin, Xiaoxue
Zhang, Haoran
Sun, Guangxi
Yang, Yaojing
Chen, Junru
Shu, Kunpeng
Zhao, Jinge
Zhao, Peng
Chen, Ni
Wang, Jia
Shen, Pengfei
Zeng, Hao
author_sort Zhang, Xingming
collection PubMed
description BACKGROUND: Due to the significant heterogeneity of renal cell carcinoma (RCC), immune checkpoints may express differently between primary and metastatic tumor. We aimed to evaluate the differential expression of TIM-3 between the primary and metastatic sites of RCC. METHODS: Cases of RCC with metastases resected or biopsied at West China Hospital between January 2009 and November 2016 were included. Clinicopathological parameters were retrospectively extracted. SPPS 22.0, GraphPad Prism 6 and R statistical software were applied for data analysis. RESULTS: A total of 163 cases were included. Immunohistochemical results showed that the overall detection rate of TIM-3 was 56.4% (92/163). The detection rate of TIM-3 in the primary (53.0%, 44/83) was numerically higher than that of the metastasis (42.6%,79/174). Although the concordance rate of TIM-3 between the primary and metastasis was as high as 66.3% (55/83) in the paired cohort, a significant statistically difference of TIM-3 expression between the primary and metastasis was observed (χ2 = 4.664, p = 0.002), with a poor consistency (Kappa = 0.331, p = 0.002). Subsequent survival analysis suggested that TIM-3 expression either in the primary or metastatic tumor was associated with longer progression-free survival (PFS) (HR: 0.67, 95% CI 0.45–0.99, P = 0.02) and overall survival (OS) (HR: 0.52, 95% CI 0.33–0.82, P < 0.001). The expressions of TIM-3 in the primary, metastatic tumors and patients treated with targeted agents all played as favorable factors for PFS and OS. Further multivariate analysis showed that, in the whole cohort, TIM-3 expression in metastatic tumor increased the predicted accuracy (PA) of the whole model of PFS from 74.7 to 75.6% (P = 0.02). For OS, the PA of whole model was increased from 78.1 to 81.1% by adding TIM-3 expression in the metastasis (P = 0.005). The same trends were also observed in paired patients and patients treated with targeted agents. In conclusion, the expression difference between the primary and metastatic tumor of TIM-3 was significant. Biopsy or resection of the metastases may provide a more accurate biological information for clinician’s decision-making and the patient’s prognosis. What’s more, the role of TIM-3 in the RCC still remains controversy, further study are needed to verify the conclusion.
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spelling pubmed-63290702019-01-16 Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma Zhang, Xingming Yin, Xiaoxue Zhang, Haoran Sun, Guangxi Yang, Yaojing Chen, Junru Shu, Kunpeng Zhao, Jinge Zhao, Peng Chen, Ni Wang, Jia Shen, Pengfei Zeng, Hao BMC Cancer Research Article BACKGROUND: Due to the significant heterogeneity of renal cell carcinoma (RCC), immune checkpoints may express differently between primary and metastatic tumor. We aimed to evaluate the differential expression of TIM-3 between the primary and metastatic sites of RCC. METHODS: Cases of RCC with metastases resected or biopsied at West China Hospital between January 2009 and November 2016 were included. Clinicopathological parameters were retrospectively extracted. SPPS 22.0, GraphPad Prism 6 and R statistical software were applied for data analysis. RESULTS: A total of 163 cases were included. Immunohistochemical results showed that the overall detection rate of TIM-3 was 56.4% (92/163). The detection rate of TIM-3 in the primary (53.0%, 44/83) was numerically higher than that of the metastasis (42.6%,79/174). Although the concordance rate of TIM-3 between the primary and metastasis was as high as 66.3% (55/83) in the paired cohort, a significant statistically difference of TIM-3 expression between the primary and metastasis was observed (χ2 = 4.664, p = 0.002), with a poor consistency (Kappa = 0.331, p = 0.002). Subsequent survival analysis suggested that TIM-3 expression either in the primary or metastatic tumor was associated with longer progression-free survival (PFS) (HR: 0.67, 95% CI 0.45–0.99, P = 0.02) and overall survival (OS) (HR: 0.52, 95% CI 0.33–0.82, P < 0.001). The expressions of TIM-3 in the primary, metastatic tumors and patients treated with targeted agents all played as favorable factors for PFS and OS. Further multivariate analysis showed that, in the whole cohort, TIM-3 expression in metastatic tumor increased the predicted accuracy (PA) of the whole model of PFS from 74.7 to 75.6% (P = 0.02). For OS, the PA of whole model was increased from 78.1 to 81.1% by adding TIM-3 expression in the metastasis (P = 0.005). The same trends were also observed in paired patients and patients treated with targeted agents. In conclusion, the expression difference between the primary and metastatic tumor of TIM-3 was significant. Biopsy or resection of the metastases may provide a more accurate biological information for clinician’s decision-making and the patient’s prognosis. What’s more, the role of TIM-3 in the RCC still remains controversy, further study are needed to verify the conclusion. BioMed Central 2019-01-10 /pmc/articles/PMC6329070/ /pubmed/30630458 http://dx.doi.org/10.1186/s12885-019-5273-5 Text en © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhang, Xingming
Yin, Xiaoxue
Zhang, Haoran
Sun, Guangxi
Yang, Yaojing
Chen, Junru
Shu, Kunpeng
Zhao, Jinge
Zhao, Peng
Chen, Ni
Wang, Jia
Shen, Pengfei
Zeng, Hao
Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma
title Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma
title_full Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma
title_fullStr Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma
title_full_unstemmed Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma
title_short Differential expression of TIM-3 between primary and metastatic sites in renal cell carcinoma
title_sort differential expression of tim-3 between primary and metastatic sites in renal cell carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329070/
https://www.ncbi.nlm.nih.gov/pubmed/30630458
http://dx.doi.org/10.1186/s12885-019-5273-5
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