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Epidemiology and screening for renal cancer
PURPOSE: The widespread use of abdominal imaging has affected the epidemiology of renal cell carcinoma (RCC). Despite this, over 25% of individuals with RCC have evidence of metastases at presentation. Screening for RCC has the potential to downstage the disease. METHODS: We performed a literature r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105141/ https://www.ncbi.nlm.nih.gov/pubmed/29610964 http://dx.doi.org/10.1007/s00345-018-2286-7 |
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author | Rossi, Sabrina H. Klatte, Tobias Usher-Smith, Juliet Stewart, Grant D. |
author_facet | Rossi, Sabrina H. Klatte, Tobias Usher-Smith, Juliet Stewart, Grant D. |
author_sort | Rossi, Sabrina H. |
collection | PubMed |
description | PURPOSE: The widespread use of abdominal imaging has affected the epidemiology of renal cell carcinoma (RCC). Despite this, over 25% of individuals with RCC have evidence of metastases at presentation. Screening for RCC has the potential to downstage the disease. METHODS: We performed a literature review on the epidemiology of RCC and evidence base regarding screening. Furthermore, contemporary RCC epidemiology data was obtained for the United Kingdom and trends in age-standardised rates of incidence and mortality were analysed by annual percentage change statistics and joinpoint regression. RESULTS: The incidence of RCC in the UK increased by 3.1% annually from 1993 through 2014. Urinary dipstick is an inadequate screening tool due to low sensitivity and specificity. It is unlikely that CT would be recommended for population screening due to cost, radiation dose and increased potential for other incidental findings. Screening ultrasound has a sensitivity and specificity of 82–83% and 98–99%, respectively; however, accuracy is dependent on tumour size. No clinically validated urinary nor serum biomarkers have been identified. Major barriers to population screening include the relatively low prevalence of the disease, the potential for false positives and over-diagnosis of slow-growing RCCs. Individual patient risk-stratification based on a combination of risk factors may improve screening efficiency and minimise harms by identifying a group at high risk of RCC. CONCLUSION: The incidence of RCC is increasing. The optimal screening modality and target population remain to be elucidated. An analysis of the benefits and harms of screening for patients and society is warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00345-018-2286-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6105141 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-61051412018-08-30 Epidemiology and screening for renal cancer Rossi, Sabrina H. Klatte, Tobias Usher-Smith, Juliet Stewart, Grant D. World J Urol Invited Review PURPOSE: The widespread use of abdominal imaging has affected the epidemiology of renal cell carcinoma (RCC). Despite this, over 25% of individuals with RCC have evidence of metastases at presentation. Screening for RCC has the potential to downstage the disease. METHODS: We performed a literature review on the epidemiology of RCC and evidence base regarding screening. Furthermore, contemporary RCC epidemiology data was obtained for the United Kingdom and trends in age-standardised rates of incidence and mortality were analysed by annual percentage change statistics and joinpoint regression. RESULTS: The incidence of RCC in the UK increased by 3.1% annually from 1993 through 2014. Urinary dipstick is an inadequate screening tool due to low sensitivity and specificity. It is unlikely that CT would be recommended for population screening due to cost, radiation dose and increased potential for other incidental findings. Screening ultrasound has a sensitivity and specificity of 82–83% and 98–99%, respectively; however, accuracy is dependent on tumour size. No clinically validated urinary nor serum biomarkers have been identified. Major barriers to population screening include the relatively low prevalence of the disease, the potential for false positives and over-diagnosis of slow-growing RCCs. Individual patient risk-stratification based on a combination of risk factors may improve screening efficiency and minimise harms by identifying a group at high risk of RCC. CONCLUSION: The incidence of RCC is increasing. The optimal screening modality and target population remain to be elucidated. An analysis of the benefits and harms of screening for patients and society is warranted. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00345-018-2286-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-04-02 2018 /pmc/articles/PMC6105141/ /pubmed/29610964 http://dx.doi.org/10.1007/s00345-018-2286-7 Text en © The Author(s) 2018 Open AccessThis 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. |
spellingShingle | Invited Review Rossi, Sabrina H. Klatte, Tobias Usher-Smith, Juliet Stewart, Grant D. Epidemiology and screening for renal cancer |
title | Epidemiology and screening for renal cancer |
title_full | Epidemiology and screening for renal cancer |
title_fullStr | Epidemiology and screening for renal cancer |
title_full_unstemmed | Epidemiology and screening for renal cancer |
title_short | Epidemiology and screening for renal cancer |
title_sort | epidemiology and screening for renal cancer |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105141/ https://www.ncbi.nlm.nih.gov/pubmed/29610964 http://dx.doi.org/10.1007/s00345-018-2286-7 |
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