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Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse
Testicular germ cell tumours (TGCTs) are the most common cause of cancer in men between the ages of 15 and 40 years, and, overall, the majority of patients should expect to be cured. The European Germ Cell Cancer Consensus Group has provided clear guidelines for the primary treatment of both seminom...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441965/ https://www.ncbi.nlm.nih.gov/pubmed/18542063 http://dx.doi.org/10.1038/sj.bjc.6604280 |
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author | van As, N J Gilbert, D C Money-Kyrle, J Bloomfield, D Beesley, S Dearnaley, D P Horwich, A Huddart, R A |
author_facet | van As, N J Gilbert, D C Money-Kyrle, J Bloomfield, D Beesley, S Dearnaley, D P Horwich, A Huddart, R A |
author_sort | van As, N J |
collection | PubMed |
description | Testicular germ cell tumours (TGCTs) are the most common cause of cancer in men between the ages of 15 and 40 years, and, overall, the majority of patients should expect to be cured. The European Germ Cell Cancer Consensus Group has provided clear guidelines for the primary treatment of both seminoma and nonseminomatous germ cell tumours. There is, however, no international consensus on how best to follow patients after their initial management. This must promptly and reliably identify relapses without causing further harm. The standardising of follow-up would result in optimising risk-benefit ratios for individual patients, while ensuring economic use of resources. We have identified the seven common scenarios in managing seminomas and nonseminomas of the various stages and discuss the pertinent issues around relapse and follow-up. We review the available literature and present our comprehensive TGCT follow-up guidelines. Our protocols provide a pragmatic, easily accessible user-friendly basis for other centres to use or to adapt to suit their needs. Furthermore, this should enable future trials to address specific issues around follow-up giving meaningful and useful results. |
format | Text |
id | pubmed-2441965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-24419652009-09-10 Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse van As, N J Gilbert, D C Money-Kyrle, J Bloomfield, D Beesley, S Dearnaley, D P Horwich, A Huddart, R A Br J Cancer Guidelines Testicular germ cell tumours (TGCTs) are the most common cause of cancer in men between the ages of 15 and 40 years, and, overall, the majority of patients should expect to be cured. The European Germ Cell Cancer Consensus Group has provided clear guidelines for the primary treatment of both seminoma and nonseminomatous germ cell tumours. There is, however, no international consensus on how best to follow patients after their initial management. This must promptly and reliably identify relapses without causing further harm. The standardising of follow-up would result in optimising risk-benefit ratios for individual patients, while ensuring economic use of resources. We have identified the seven common scenarios in managing seminomas and nonseminomas of the various stages and discuss the pertinent issues around relapse and follow-up. We review the available literature and present our comprehensive TGCT follow-up guidelines. Our protocols provide a pragmatic, easily accessible user-friendly basis for other centres to use or to adapt to suit their needs. Furthermore, this should enable future trials to address specific issues around follow-up giving meaningful and useful results. Nature Publishing Group 2008-06-17 2008-06-10 /pmc/articles/PMC2441965/ /pubmed/18542063 http://dx.doi.org/10.1038/sj.bjc.6604280 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Guidelines van As, N J Gilbert, D C Money-Kyrle, J Bloomfield, D Beesley, S Dearnaley, D P Horwich, A Huddart, R A Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
title | Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
title_full | Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
title_fullStr | Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
title_full_unstemmed | Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
title_short | Evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
title_sort | evidence-based pragmatic guidelines for the follow-up of testicular cancer: optimising the detection of relapse |
topic | Guidelines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2441965/ https://www.ncbi.nlm.nih.gov/pubmed/18542063 http://dx.doi.org/10.1038/sj.bjc.6604280 |
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