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Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative
BACKGROUND: The past three decades have seen rapid improvements in the diagnosis and treatment of most cancers and the most important contributor has been research. Progress in rare cancers has been slower, not least because of the challenges of undertaking research. SETTINGS: The International Rare...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639696/ https://www.ncbi.nlm.nih.gov/pubmed/25542058 http://dx.doi.org/10.1016/j.ejca.2014.10.027 |
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author | Bogaerts, Jan Sydes, Matthew R. Keat, Nicola McConnell, Andrea Benson, Al Ho, Alan Roth, Arnaud Fortpied, Catherine Eng, Cathy Peckitt, Clare Coens, Corneel Pettaway, Curtis Arnold, Dirk Hall, Emma Marshall, Ernie Sclafani, Francesco Hatcher, Helen Earl, Helena Ray-Coquard, Isabelle Paul, James Blay, Jean-Yves Whelan, Jeremy Panageas, Kathy Wheatley, Keith Harrington, Kevin Licitra, Lisa Billingham, Lucinda Hensley, Martee McCabe, Martin Patel, Poulam M. Carvajal, Richard Wilson, Richard Glynne-Jones, Rob McWilliams, Rob Leyvraz, Serge Rao, Sheela Nicholson, Steve Filiaci, Virginia Negrouk, Anastassia Lacombe, Denis Dupont, Elisabeth Pauporté, Iris Welch, John J. Law, Kate Trimble, Ted Seymour, Matthew |
author_facet | Bogaerts, Jan Sydes, Matthew R. Keat, Nicola McConnell, Andrea Benson, Al Ho, Alan Roth, Arnaud Fortpied, Catherine Eng, Cathy Peckitt, Clare Coens, Corneel Pettaway, Curtis Arnold, Dirk Hall, Emma Marshall, Ernie Sclafani, Francesco Hatcher, Helen Earl, Helena Ray-Coquard, Isabelle Paul, James Blay, Jean-Yves Whelan, Jeremy Panageas, Kathy Wheatley, Keith Harrington, Kevin Licitra, Lisa Billingham, Lucinda Hensley, Martee McCabe, Martin Patel, Poulam M. Carvajal, Richard Wilson, Richard Glynne-Jones, Rob McWilliams, Rob Leyvraz, Serge Rao, Sheela Nicholson, Steve Filiaci, Virginia Negrouk, Anastassia Lacombe, Denis Dupont, Elisabeth Pauporté, Iris Welch, John J. Law, Kate Trimble, Ted Seymour, Matthew |
author_sort | Bogaerts, Jan |
collection | PubMed |
description | BACKGROUND: The past three decades have seen rapid improvements in the diagnosis and treatment of most cancers and the most important contributor has been research. Progress in rare cancers has been slower, not least because of the challenges of undertaking research. SETTINGS: The International Rare Cancers Initiative (IRCI) is a partnership which aims to stimulate and facilitate the development of international clinical trials for patients with rare cancers. It is focused on interventional – usually randomised – clinical trials with the clear goal of improving outcomes for patients. The key challenges are organisational and methodological. A multi-disciplinary workshop to review the methods used in ICRI portfolio trials was held in Amsterdam in September 2013. Other as-yet unrealised methods were also discussed. RESULTS: The IRCI trials are each presented to exemplify possible approaches to designing credible trials in rare cancers. Researchers may consider these for use in future trials and understand the choices made for each design. INTERPRETATION: Trials can be designed using a wide array of possibilities. There is no ‘one size fits all’ solution. In order to make progress in the rare diseases, decisions to change practice will have to be based on less direct evidence from clinical trials than in more common diseases. |
format | Online Article Text |
id | pubmed-4639696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-46396962015-11-10 Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative Bogaerts, Jan Sydes, Matthew R. Keat, Nicola McConnell, Andrea Benson, Al Ho, Alan Roth, Arnaud Fortpied, Catherine Eng, Cathy Peckitt, Clare Coens, Corneel Pettaway, Curtis Arnold, Dirk Hall, Emma Marshall, Ernie Sclafani, Francesco Hatcher, Helen Earl, Helena Ray-Coquard, Isabelle Paul, James Blay, Jean-Yves Whelan, Jeremy Panageas, Kathy Wheatley, Keith Harrington, Kevin Licitra, Lisa Billingham, Lucinda Hensley, Martee McCabe, Martin Patel, Poulam M. Carvajal, Richard Wilson, Richard Glynne-Jones, Rob McWilliams, Rob Leyvraz, Serge Rao, Sheela Nicholson, Steve Filiaci, Virginia Negrouk, Anastassia Lacombe, Denis Dupont, Elisabeth Pauporté, Iris Welch, John J. Law, Kate Trimble, Ted Seymour, Matthew Eur J Cancer Review BACKGROUND: The past three decades have seen rapid improvements in the diagnosis and treatment of most cancers and the most important contributor has been research. Progress in rare cancers has been slower, not least because of the challenges of undertaking research. SETTINGS: The International Rare Cancers Initiative (IRCI) is a partnership which aims to stimulate and facilitate the development of international clinical trials for patients with rare cancers. It is focused on interventional – usually randomised – clinical trials with the clear goal of improving outcomes for patients. The key challenges are organisational and methodological. A multi-disciplinary workshop to review the methods used in ICRI portfolio trials was held in Amsterdam in September 2013. Other as-yet unrealised methods were also discussed. RESULTS: The IRCI trials are each presented to exemplify possible approaches to designing credible trials in rare cancers. Researchers may consider these for use in future trials and understand the choices made for each design. INTERPRETATION: Trials can be designed using a wide array of possibilities. There is no ‘one size fits all’ solution. In order to make progress in the rare diseases, decisions to change practice will have to be based on less direct evidence from clinical trials than in more common diseases. Elsevier Science Ltd 2015-02 /pmc/articles/PMC4639696/ /pubmed/25542058 http://dx.doi.org/10.1016/j.ejca.2014.10.027 Text en © 2014 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Review Bogaerts, Jan Sydes, Matthew R. Keat, Nicola McConnell, Andrea Benson, Al Ho, Alan Roth, Arnaud Fortpied, Catherine Eng, Cathy Peckitt, Clare Coens, Corneel Pettaway, Curtis Arnold, Dirk Hall, Emma Marshall, Ernie Sclafani, Francesco Hatcher, Helen Earl, Helena Ray-Coquard, Isabelle Paul, James Blay, Jean-Yves Whelan, Jeremy Panageas, Kathy Wheatley, Keith Harrington, Kevin Licitra, Lisa Billingham, Lucinda Hensley, Martee McCabe, Martin Patel, Poulam M. Carvajal, Richard Wilson, Richard Glynne-Jones, Rob McWilliams, Rob Leyvraz, Serge Rao, Sheela Nicholson, Steve Filiaci, Virginia Negrouk, Anastassia Lacombe, Denis Dupont, Elisabeth Pauporté, Iris Welch, John J. Law, Kate Trimble, Ted Seymour, Matthew Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative |
title | Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative |
title_full | Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative |
title_fullStr | Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative |
title_full_unstemmed | Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative |
title_short | Clinical trial designs for rare diseases: Studies developed and discussed by the International Rare Cancers Initiative |
title_sort | clinical trial designs for rare diseases: studies developed and discussed by the international rare cancers initiative |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4639696/ https://www.ncbi.nlm.nih.gov/pubmed/25542058 http://dx.doi.org/10.1016/j.ejca.2014.10.027 |
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