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First published online June 9, 2008
British Journal of Radiology (2008) 81, 685-692
© 2008 British Institute of Radiology
doi: 10.1259/bjr/16768437

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British Journal of Radiology 81 (2008),685-692 ©2008 The British Institute of Radiology

Review Article

The role of clinical imaging in oncological drug development

P S MURPHY, PhD, MRSC1, T J McCARTHY, PhD2 and A S K DZIK-JURASZ, PhD, FRCR, FRCS3

1 Pfizer Global Research and Development, Sandwich, Kent, UK, 2 Pfizer Global Research and Development, Groton, CT, USA, 3 Novartis Pharmaceuticals Corporation, One Health Plaza, East Hanover, NJ, USA

Correspondence: Philip S Murphy, Oncology Medicines Development Center, GlaxoSmithKline Research and Development Limited, Stockley Park West, Uxbridge, Middlesex UB11 1BT, UK. E-mail: philip.s.murphy{at}gsk.com

Clinical imaging has the potential to provide key biomarkers to inform decision-making in drug development. There is considerable optimism that emerging functional imaging techniques will substantially add to the conventional morphological depiction of disease. The discovery, development and qualification of clinical imaging biomarkers remain a considerable undertaking. Once an imaging biomarker is developed, it must be implemented with a high degree of consistency to ensure the collection of robust clinical trial data. The aim of such a development and implementation process is to deliver sufficient confidence in an imaging biomarker to support "go/no-go" decisions made in a drug development programme. This article outlines the drug development process, with a focus on the current impact of clinical imaging on drug development and its probable future direction.







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