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Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials
The identification of new surrogate endpoints for advanced colorectal cancer is becoming crucial and, along with drug development, it represents a research field increasingly studied. Although overall survival (OS) remains the strongest trial endpoint available, it requires larger sample size and lo...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745687/ https://www.ncbi.nlm.nih.gov/pubmed/26308250 |
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author | Aprile, Giuseppe Fontanella, Caterina Bonotto, Marta Rihawi, Karim Lutrino, Stefania Eufemia Ferrari, Laura Casagrande, Mariaelena Ongaro, Elena Berretta, Massimiliano Avallone, Antonio Rosati, Gerardo Giuliani, Francesco Fasola, Gianpiero |
author_facet | Aprile, Giuseppe Fontanella, Caterina Bonotto, Marta Rihawi, Karim Lutrino, Stefania Eufemia Ferrari, Laura Casagrande, Mariaelena Ongaro, Elena Berretta, Massimiliano Avallone, Antonio Rosati, Gerardo Giuliani, Francesco Fasola, Gianpiero |
author_sort | Aprile, Giuseppe |
collection | PubMed |
description | The identification of new surrogate endpoints for advanced colorectal cancer is becoming crucial and, along with drug development, it represents a research field increasingly studied. Although overall survival (OS) remains the strongest trial endpoint available, it requires larger sample size and longer periods of time for an event to happen. Surrogate endpoints such as progression free survival (PFS) or response rate (RR) may overcome these issues but, as such, they need to be prospectively validated before replacing the real endpoints; moreover, they often bear many other limitations. In this narrative review we initially discuss the role of time-to-event endpoints, objective response and response rate as surrogates of OS in the advanced colorectal cancer setting, discussing also how such measures are influenced by the tumor assessment criteria currently employed. We then report recent data published about early tumor shrinkage and deepness of response, which have recently emerged as novel potential endpoint surrogates, discussing their strengths and weaknesses and providing a critical comment. Despite being very compelling, the role of such novel response measures is yet to be confirmed and their surrogacy with OS still needs to be further investigated within larger and well-designed trials. |
format | Online Article Text |
id | pubmed-4745687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47456872016-02-23 Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials Aprile, Giuseppe Fontanella, Caterina Bonotto, Marta Rihawi, Karim Lutrino, Stefania Eufemia Ferrari, Laura Casagrande, Mariaelena Ongaro, Elena Berretta, Massimiliano Avallone, Antonio Rosati, Gerardo Giuliani, Francesco Fasola, Gianpiero Oncotarget Review The identification of new surrogate endpoints for advanced colorectal cancer is becoming crucial and, along with drug development, it represents a research field increasingly studied. Although overall survival (OS) remains the strongest trial endpoint available, it requires larger sample size and longer periods of time for an event to happen. Surrogate endpoints such as progression free survival (PFS) or response rate (RR) may overcome these issues but, as such, they need to be prospectively validated before replacing the real endpoints; moreover, they often bear many other limitations. In this narrative review we initially discuss the role of time-to-event endpoints, objective response and response rate as surrogates of OS in the advanced colorectal cancer setting, discussing also how such measures are influenced by the tumor assessment criteria currently employed. We then report recent data published about early tumor shrinkage and deepness of response, which have recently emerged as novel potential endpoint surrogates, discussing their strengths and weaknesses and providing a critical comment. Despite being very compelling, the role of such novel response measures is yet to be confirmed and their surrogacy with OS still needs to be further investigated within larger and well-designed trials. Impact Journals LLC 2015-07-23 /pmc/articles/PMC4745687/ /pubmed/26308250 Text en Copyright: © 2015 Aprile et al. http://creativecommons.org/licenses/by/2.5/ 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 author and source are credited. |
spellingShingle | Review Aprile, Giuseppe Fontanella, Caterina Bonotto, Marta Rihawi, Karim Lutrino, Stefania Eufemia Ferrari, Laura Casagrande, Mariaelena Ongaro, Elena Berretta, Massimiliano Avallone, Antonio Rosati, Gerardo Giuliani, Francesco Fasola, Gianpiero Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
title | Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
title_full | Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
title_fullStr | Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
title_full_unstemmed | Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
title_short | Timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
title_sort | timing and extent of response in colorectal cancer: critical review of current data and implication for future trials |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745687/ https://www.ncbi.nlm.nih.gov/pubmed/26308250 |
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