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Speeding up the Evaluation of New Agents in Cancer

Despite both the increase in basic biologic knowledge and the fact that many new agents have reached various stages of development during the last 10 years, the number of new treatments that have been approved for patients has not increased as expected. We propose the multi-arm, multi-stage trial de...

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Autores principales: Parmar, Mahesh K. B., Barthel, Friederike. M.-S., Sydes, Matthew, Langley, Ruth, Kaplan, Rick, Eisenhauer, Elizabeth, Brady, Mark, James, Nicholas, Bookman, Michael A., Swart, Ann-Marie, Qian, Wendi, Royston, Patrick
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528020/
https://www.ncbi.nlm.nih.gov/pubmed/18728279
http://dx.doi.org/10.1093/jnci/djn267
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author Parmar, Mahesh K. B.
Barthel, Friederike. M.-S.
Sydes, Matthew
Langley, Ruth
Kaplan, Rick
Eisenhauer, Elizabeth
Brady, Mark
James, Nicholas
Bookman, Michael A.
Swart, Ann-Marie
Qian, Wendi
Royston, Patrick
author_facet Parmar, Mahesh K. B.
Barthel, Friederike. M.-S.
Sydes, Matthew
Langley, Ruth
Kaplan, Rick
Eisenhauer, Elizabeth
Brady, Mark
James, Nicholas
Bookman, Michael A.
Swart, Ann-Marie
Qian, Wendi
Royston, Patrick
author_sort Parmar, Mahesh K. B.
collection PubMed
description Despite both the increase in basic biologic knowledge and the fact that many new agents have reached various stages of development during the last 10 years, the number of new treatments that have been approved for patients has not increased as expected. We propose the multi-arm, multi-stage trial design as a way to evaluate treatments faster and more efficiently than current standard trial designs. By using intermediate outcomes and testing a number of new agents (and combinations) simultaneously, the new design requires fewer patients. Three trials using this methodology are presented.
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spelling pubmed-25280202009-02-25 Speeding up the Evaluation of New Agents in Cancer Parmar, Mahesh K. B. Barthel, Friederike. M.-S. Sydes, Matthew Langley, Ruth Kaplan, Rick Eisenhauer, Elizabeth Brady, Mark James, Nicholas Bookman, Michael A. Swart, Ann-Marie Qian, Wendi Royston, Patrick J Natl Cancer Inst Commentary Despite both the increase in basic biologic knowledge and the fact that many new agents have reached various stages of development during the last 10 years, the number of new treatments that have been approved for patients has not increased as expected. We propose the multi-arm, multi-stage trial design as a way to evaluate treatments faster and more efficiently than current standard trial designs. By using intermediate outcomes and testing a number of new agents (and combinations) simultaneously, the new design requires fewer patients. Three trials using this methodology are presented. Oxford University Press 2008-09-03 2008-09-03 /pmc/articles/PMC2528020/ /pubmed/18728279 http://dx.doi.org/10.1093/jnci/djn267 Text en © 2008 The Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Parmar, Mahesh K. B.
Barthel, Friederike. M.-S.
Sydes, Matthew
Langley, Ruth
Kaplan, Rick
Eisenhauer, Elizabeth
Brady, Mark
James, Nicholas
Bookman, Michael A.
Swart, Ann-Marie
Qian, Wendi
Royston, Patrick
Speeding up the Evaluation of New Agents in Cancer
title Speeding up the Evaluation of New Agents in Cancer
title_full Speeding up the Evaluation of New Agents in Cancer
title_fullStr Speeding up the Evaluation of New Agents in Cancer
title_full_unstemmed Speeding up the Evaluation of New Agents in Cancer
title_short Speeding up the Evaluation of New Agents in Cancer
title_sort speeding up the evaluation of new agents in cancer
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528020/
https://www.ncbi.nlm.nih.gov/pubmed/18728279
http://dx.doi.org/10.1093/jnci/djn267
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