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dc.contributor.authorRanson, Malcolm R
dc.contributor.authorJayson, Gordon C
dc.date.accessioned2009-07-29T10:57:09Z
dc.date.available2009-07-29T10:57:09Z
dc.date.issued2005-06
dc.identifier.citationTargeted antitumour therapy--future perspectives. 2005, 92 Suppl 1:S28-31 Br. J. Canceren
dc.identifier.issn0007-0920
dc.identifier.pmid15928656
dc.identifier.doi10.1038/sj.bjc.6602606
dc.identifier.urihttp://hdl.handle.net/10541/75816
dc.description.abstractThe advent of targeted therapy presents an unprecedented opportunity for advances in the treatment of cancer. A key challenge will be to translate the undoubted promise of targeted agents into tangible clinical benefits. Achieving this goal is likely to be dependent upon a number of factors. These include continued research to improve our understanding of the heterogeneity and complexity of the tumour microenvironment; refinement of clinical trial design to incorporate nontraditional end points such as the optimum biological dose and health-related quality of life; and the use of technological advancements in proteomics, genomics and biomarker development to better predict tumour types and patient subsets that may be particularly responsive to treatment, as well as enable a more accurate assessment of drug effect at the molecular level. In summary, the future success of targeted agents will require an integrated multidisciplinary approach involving all stakeholders.
dc.language.isoenen
dc.subjectCanceren
dc.subjectTumour Markersen
dc.subject.meshAntibodies, Monoclonal
dc.subject.meshBiomedical Research
dc.subject.meshClinical Trials as Topic
dc.subject.meshForecasting
dc.subject.meshHumans
dc.subject.meshNeoplasms
dc.subject.meshQuality of Life
dc.subject.meshResearch Design
dc.subject.meshTumor Markers, Biological
dc.titleTargeted antitumour therapy--future perspectives.en
dc.typeArticleen
dc.contributor.departmentDepartment of Medical Oncology, University of Manchester, Christie Hospital NHS Trust, Wilmslow Road, Manchester M20 4BX, UK. malcolm.ranson@man.ac.uken
dc.identifier.journalBritish Journal of Canceren
html.description.abstractThe advent of targeted therapy presents an unprecedented opportunity for advances in the treatment of cancer. A key challenge will be to translate the undoubted promise of targeted agents into tangible clinical benefits. Achieving this goal is likely to be dependent upon a number of factors. These include continued research to improve our understanding of the heterogeneity and complexity of the tumour microenvironment; refinement of clinical trial design to incorporate nontraditional end points such as the optimum biological dose and health-related quality of life; and the use of technological advancements in proteomics, genomics and biomarker development to better predict tumour types and patient subsets that may be particularly responsive to treatment, as well as enable a more accurate assessment of drug effect at the molecular level. In summary, the future success of targeted agents will require an integrated multidisciplinary approach involving all stakeholders.


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