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Clinical research in oncology: in memory of Professor Gordon McVie

Gordon McVie campaigned throughout his career for merging scientific and clinical expertise and for investigating the underlying pharmacokinetics and pharmacodynamics in clinical trials. This need remains highly relevant today when most cancer clinical trials investigate agents that target a known m...

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Detalles Bibliográficos
Autor principal: Tannock, Ian F
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831109/
https://www.ncbi.nlm.nih.gov/pubmed/35242221
http://dx.doi.org/10.3332/ecancer.2022.1340
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author Tannock, Ian F
author_facet Tannock, Ian F
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description Gordon McVie campaigned throughout his career for merging scientific and clinical expertise and for investigating the underlying pharmacokinetics and pharmacodynamics in clinical trials. This need remains highly relevant today when most cancer clinical trials investigate agents that target a known molecular pathway, yet anticancer drug development has changed minimally from that used for chemotherapy when more was better and substantial toxicity inevitable. Here, I summarise some common problems that confound current drug development, including problems in interpreting results of phase 3 randomised trials, as well as trials investigating personalised medicine.
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spelling pubmed-88311092022-03-02 Clinical research in oncology: in memory of Professor Gordon McVie Tannock, Ian F Ecancermedicalscience Short Communication Gordon McVie campaigned throughout his career for merging scientific and clinical expertise and for investigating the underlying pharmacokinetics and pharmacodynamics in clinical trials. This need remains highly relevant today when most cancer clinical trials investigate agents that target a known molecular pathway, yet anticancer drug development has changed minimally from that used for chemotherapy when more was better and substantial toxicity inevitable. Here, I summarise some common problems that confound current drug development, including problems in interpreting results of phase 3 randomised trials, as well as trials investigating personalised medicine. Cancer Intelligence 2022-01-13 /pmc/articles/PMC8831109/ /pubmed/35242221 http://dx.doi.org/10.3332/ecancer.2022.1340 Text en © the authors; licensee ecancermedicalscience. https://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 (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Tannock, Ian F
Clinical research in oncology: in memory of Professor Gordon McVie
title Clinical research in oncology: in memory of Professor Gordon McVie
title_full Clinical research in oncology: in memory of Professor Gordon McVie
title_fullStr Clinical research in oncology: in memory of Professor Gordon McVie
title_full_unstemmed Clinical research in oncology: in memory of Professor Gordon McVie
title_short Clinical research in oncology: in memory of Professor Gordon McVie
title_sort clinical research in oncology: in memory of professor gordon mcvie
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8831109/
https://www.ncbi.nlm.nih.gov/pubmed/35242221
http://dx.doi.org/10.3332/ecancer.2022.1340
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