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Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer

Long-term follow-up is an important unmet need for the full analysis of new treatments for cancer. Earlier detection of cancer and more effective treatment have led to many more patients surviving for more than 5 and even 10 years, so that evaluating late recurrences and side-effects is an increasin...

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Autor principal: Cuzick, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658544/
https://www.ncbi.nlm.nih.gov/pubmed/26433395
http://dx.doi.org/10.1093/annonc/mdv392
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author Cuzick, J.
author_facet Cuzick, J.
author_sort Cuzick, J.
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description Long-term follow-up is an important unmet need for the full analysis of new treatments for cancer. Earlier detection of cancer and more effective treatment have led to many more patients surviving for more than 5 and even 10 years, so that evaluating late recurrences and side-effects is an increasingly important issue. This is particularly relevant for oestrogen receptor-positive breast cancer, where the existence of late recurrences is well documented. However, survival for other cancers, notably prostate, colorectal and cervix cancer, has dramatically increased in recent years due to screening and better treatment of early lesions. Trials of preventive therapies have an even greater need for long follow-up. Here, we review these issues and suggest ways in which provision for long-term follow-up can be improved.
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spelling pubmed-46585442015-11-26 Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer Cuzick, J. Ann Oncol Special Article Long-term follow-up is an important unmet need for the full analysis of new treatments for cancer. Earlier detection of cancer and more effective treatment have led to many more patients surviving for more than 5 and even 10 years, so that evaluating late recurrences and side-effects is an increasingly important issue. This is particularly relevant for oestrogen receptor-positive breast cancer, where the existence of late recurrences is well documented. However, survival for other cancers, notably prostate, colorectal and cervix cancer, has dramatically increased in recent years due to screening and better treatment of early lesions. Trials of preventive therapies have an even greater need for long follow-up. Here, we review these issues and suggest ways in which provision for long-term follow-up can be improved. Oxford University Press 2015-12 2015-10-03 /pmc/articles/PMC4658544/ /pubmed/26433395 http://dx.doi.org/10.1093/annonc/mdv392 Text en © The Author 2015. Published by Oxford University Press on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Special Article
Cuzick, J.
Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
title Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
title_full Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
title_fullStr Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
title_full_unstemmed Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
title_short Statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
title_sort statistical controversies in clinical research: long-term follow-up of clinical trials in cancer
topic Special Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658544/
https://www.ncbi.nlm.nih.gov/pubmed/26433395
http://dx.doi.org/10.1093/annonc/mdv392
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