4.7 Review

Development of radiotracers for oncology - the interface with pharmacology

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 163, Issue 8, Pages 1565-1585

Publisher

WILEY
DOI: 10.1111/j.1476-5381.2010.01160.x

Keywords

positron emission tomography (PET); radioisotope; drug development; radiopharmaceutical

Funding

  1. Cancer Research UK/Engineering and Physical Sciences Research Council/Medical Research Council/National Institute for Health Research [C2536/A10337]
  2. MRC [MC_U120081322] Funding Source: UKRI
  3. Cancer Research UK [10337] Funding Source: researchfish
  4. Medical Research Council [MC_U120081322] Funding Source: researchfish

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There is an increasing role for positron emission tomography (PET) in oncology, particularly as a component of early phase clinical trials. As a non-invasive functional imaging modality, PET can be used to assess both pharmacokinetics and pharmacodynamics of novel therapeutics by utilizing radiolabelled compounds. These studies can provide crucial information early in the drug development process that may influence the further development of novel therapeutics. PET imaging probes can also be used as early biomarkers of clinical response and to predict clinical outcome prior to the administration of therapeutic agents. We discuss the role of PET imaging particularly as applied to phase 0 studies and discuss the regulations involved in the development and synthesis of novel radioligands. The review also discusses currently available tracers and their role in the assessment of pharmacokinetics and pharmacodynamics as applied to oncology.

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