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Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis
PURPOSE: To explore the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model application for predicting outcome of patients with metastatic renal cell carcinoma using targeted agents. MATERIALS AND METHODS: We performed a literature review of 989 articles. The selecting pro...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Urologia
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088475/ https://www.ncbi.nlm.nih.gov/pubmed/31961626 http://dx.doi.org/10.1590/S1677-5538.IBJU.2019.0423 |
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author | Jiang, Guiya Chen, Shuqiu Chen, Ming |
author_facet | Jiang, Guiya Chen, Shuqiu Chen, Ming |
author_sort | Jiang, Guiya |
collection | PubMed |
description | PURPOSE: To explore the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model application for predicting outcome of patients with metastatic renal cell carcinoma using targeted agents. MATERIALS AND METHODS: We performed a literature review of 989 articles. The selecting process used preferred reporting items for systematic reviews and meta-analyses (PRISMA). All included studies were assessed by Newcastle-Ottawa scale. Results of individual studies were pooled using Stata 14.0 software. RESULTS: A total of 17 articles were included. Most articles provided univariate and multivariate analysis of IMDC model prognosis. Combined HRs were 1.58 (95% CI 1.34-1.82) and 3.74 (95% CI 2.67-4.81) for univariate PFS of intermediate to favorable and poor to favorable respectively. In the category of multivariate PFS, combined HRs were 1.27 (95% CI 0.99-1.56) and 2.29 (95% CI 1.65-2.93) with intermediate to favorable and poor to favorable respectively. Regarding univariate OS, combined HRs were 1.93 (95% CI 1.62-2.24) and 6.25 (95% CI 4.18-8.31) with intermediate to favorable and poor to favorable respectively. With multivariate OS, combined HRs were 1.32 (95%CI 1.04-1.59) and 2.35 (95%CI 1.69-3.01) with intermediate to favorable and poor to favorable respectively. CONCLUSION: In summary, analysis of currently available clinical evidence indicated that IMDC model could be applied to classify patients with metastatic renal cell carcinoma using targeted agents. However, different types of targeted agents and various areas could affect the accuracy of the model. There was also a difference in predicting patients' PFS and OS. |
format | Online Article Text |
id | pubmed-7088475 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Sociedade Brasileira de Urologia |
record_format | MEDLINE/PubMed |
spelling | pubmed-70884752020-04-02 Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis Jiang, Guiya Chen, Shuqiu Chen, Ming Int Braz J Urol Review Article PURPOSE: To explore the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model application for predicting outcome of patients with metastatic renal cell carcinoma using targeted agents. MATERIALS AND METHODS: We performed a literature review of 989 articles. The selecting process used preferred reporting items for systematic reviews and meta-analyses (PRISMA). All included studies were assessed by Newcastle-Ottawa scale. Results of individual studies were pooled using Stata 14.0 software. RESULTS: A total of 17 articles were included. Most articles provided univariate and multivariate analysis of IMDC model prognosis. Combined HRs were 1.58 (95% CI 1.34-1.82) and 3.74 (95% CI 2.67-4.81) for univariate PFS of intermediate to favorable and poor to favorable respectively. In the category of multivariate PFS, combined HRs were 1.27 (95% CI 0.99-1.56) and 2.29 (95% CI 1.65-2.93) with intermediate to favorable and poor to favorable respectively. Regarding univariate OS, combined HRs were 1.93 (95% CI 1.62-2.24) and 6.25 (95% CI 4.18-8.31) with intermediate to favorable and poor to favorable respectively. With multivariate OS, combined HRs were 1.32 (95%CI 1.04-1.59) and 2.35 (95%CI 1.69-3.01) with intermediate to favorable and poor to favorable respectively. CONCLUSION: In summary, analysis of currently available clinical evidence indicated that IMDC model could be applied to classify patients with metastatic renal cell carcinoma using targeted agents. However, different types of targeted agents and various areas could affect the accuracy of the model. There was also a difference in predicting patients' PFS and OS. Sociedade Brasileira de Urologia 2020-02-20 /pmc/articles/PMC7088475/ /pubmed/31961626 http://dx.doi.org/10.1590/S1677-5538.IBJU.2019.0423 Text en https://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Jiang, Guiya Chen, Shuqiu Chen, Ming Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
title | Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
title_full | Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
title_fullStr | Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
title_full_unstemmed | Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
title_short | Exploration of IMDC model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
title_sort | exploration of imdc model in patients with metastatic renal cell carcinoma using targeted agents: a meta-analysis |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088475/ https://www.ncbi.nlm.nih.gov/pubmed/31961626 http://dx.doi.org/10.1590/S1677-5538.IBJU.2019.0423 |
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