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Serum markers change for intraocular metastasis in renal cell carcinoma
Objective: Renal cell carcinoma is prone to early metastasis. In general, intraocular metastasis (IOM) is not common. In the present study, we studied the relationship between different biochemical indicators and the occurrence of IOM in renal cancer patients, and identified the potential risk facto...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438111/ https://www.ncbi.nlm.nih.gov/pubmed/34467977 http://dx.doi.org/10.1042/BSR20203116 |
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author | Sun, Tie Tang, Jing Pan, Yi-Cong Yu, Chen-Yu Li, Biao Zhang, Li-Juan Shu, Hui-Ye Ge, Qian-Min Shao, Yi |
author_facet | Sun, Tie Tang, Jing Pan, Yi-Cong Yu, Chen-Yu Li, Biao Zhang, Li-Juan Shu, Hui-Ye Ge, Qian-Min Shao, Yi |
author_sort | Sun, Tie |
collection | PubMed |
description | Objective: Renal cell carcinoma is prone to early metastasis. In general, intraocular metastasis (IOM) is not common. In the present study, we studied the relationship between different biochemical indicators and the occurrence of IOM in renal cancer patients, and identified the potential risk factors. Methods: A retrospective analysis of the clinical data of 214 patients with renal cell carcinoma from October 2001 to August 2016 was carried out. The difference and correlation of various indicators between the two groups with or without IOM was analyzed, and binary logistic regression analysis was used to explore the risk factors of IOM in renal cancer patients. The diagnostic value of each independent related factor was calculated according to the receiver operating curve (ROC). Results: The level of neuron-specific enolase (NSE) in renal cell carcinoma patients with IOM was significantly higher than that in patients without IOM (P<0.05). There was no significant difference in alkaline phosphatase (ALP), hemoglobin (Hb), serum calcium concentration, α fetoprotein (AFP), carcinoembryonic antigen (CEA), CA-125 etc. between IOM group and non-IOM (NIOM) group (P>0.05). Binary logistic regression analysis showed that NSE was an independent risk factor for IOM in renal cell carcinoma patients (P<0.05). ROC curve shows that the factor has high accuracy in predicting IOM, and the area under the curve (AUC) is 0.774. The cut-off value of NSE was 49.5 U/l, the sensitivity was 72.2% and the specificity was 80.1%. Conclusion: NSE concentration is a risk factor for IOM in patients with renal cell cancer. If the concentration of NSE in the patient’s body is ≥49.5 U/l, disease monitoring and eye scans should be strengthened. |
format | Online Article Text |
id | pubmed-8438111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84381112021-09-21 Serum markers change for intraocular metastasis in renal cell carcinoma Sun, Tie Tang, Jing Pan, Yi-Cong Yu, Chen-Yu Li, Biao Zhang, Li-Juan Shu, Hui-Ye Ge, Qian-Min Shao, Yi Biosci Rep Cancer Objective: Renal cell carcinoma is prone to early metastasis. In general, intraocular metastasis (IOM) is not common. In the present study, we studied the relationship between different biochemical indicators and the occurrence of IOM in renal cancer patients, and identified the potential risk factors. Methods: A retrospective analysis of the clinical data of 214 patients with renal cell carcinoma from October 2001 to August 2016 was carried out. The difference and correlation of various indicators between the two groups with or without IOM was analyzed, and binary logistic regression analysis was used to explore the risk factors of IOM in renal cancer patients. The diagnostic value of each independent related factor was calculated according to the receiver operating curve (ROC). Results: The level of neuron-specific enolase (NSE) in renal cell carcinoma patients with IOM was significantly higher than that in patients without IOM (P<0.05). There was no significant difference in alkaline phosphatase (ALP), hemoglobin (Hb), serum calcium concentration, α fetoprotein (AFP), carcinoembryonic antigen (CEA), CA-125 etc. between IOM group and non-IOM (NIOM) group (P>0.05). Binary logistic regression analysis showed that NSE was an independent risk factor for IOM in renal cell carcinoma patients (P<0.05). ROC curve shows that the factor has high accuracy in predicting IOM, and the area under the curve (AUC) is 0.774. The cut-off value of NSE was 49.5 U/l, the sensitivity was 72.2% and the specificity was 80.1%. Conclusion: NSE concentration is a risk factor for IOM in patients with renal cell cancer. If the concentration of NSE in the patient’s body is ≥49.5 U/l, disease monitoring and eye scans should be strengthened. Portland Press Ltd. 2021-09-13 /pmc/articles/PMC8438111/ /pubmed/34467977 http://dx.doi.org/10.1042/BSR20203116 Text en © 2021 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Cancer Sun, Tie Tang, Jing Pan, Yi-Cong Yu, Chen-Yu Li, Biao Zhang, Li-Juan Shu, Hui-Ye Ge, Qian-Min Shao, Yi Serum markers change for intraocular metastasis in renal cell carcinoma |
title | Serum markers change for intraocular metastasis in renal cell carcinoma |
title_full | Serum markers change for intraocular metastasis in renal cell carcinoma |
title_fullStr | Serum markers change for intraocular metastasis in renal cell carcinoma |
title_full_unstemmed | Serum markers change for intraocular metastasis in renal cell carcinoma |
title_short | Serum markers change for intraocular metastasis in renal cell carcinoma |
title_sort | serum markers change for intraocular metastasis in renal cell carcinoma |
topic | Cancer |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438111/ https://www.ncbi.nlm.nih.gov/pubmed/34467977 http://dx.doi.org/10.1042/BSR20203116 |
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