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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Cancer Intelligence
2022
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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 |
author_sort | Tannock, Ian F |
collection | PubMed |
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. |
format | Online Article Text |
id | pubmed-8831109 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cancer Intelligence |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT tannockianf clinicalresearchinoncologyinmemoryofprofessorgordonmcvie |