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PET for in vivo pharmacokinetic and pharmacodynamic measurements
Positron emission tomography (PET) scanning is evolving as a unique tool for drug development in oncology for improving both the efficacy of established treatment and in evaluating novel anticancer agents. As a non-invasive functional imaging modality, PET has an unrivalled sensitivity when monitori...
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Published in: | European journal of cancer (1990) 2002-11, Vol.38 (16), p.2094-2107 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Positron emission tomography (PET) scanning is evolving as a unique tool for drug development in oncology for improving both the efficacy of established treatment and in evaluating novel anticancer agents. As a non-invasive functional imaging modality, PET has an unrivalled sensitivity when monitoring the pharmacokinetics and pharmacodynamics of drugs and biochemicals when radiolabelled with short living positron-emitting radioisotopes. This is of particular relevance in assessing newer molecular-targeted therapy where conventional evaluation criteria (maximum tolerated dose and tumour shrinkage for example) may be inappropriate. PET has already been applied to a wide number of drugs to demonstrate activity
in vivo from standard chemotherapy such as 5-fluorouracil (5-FU) [
J Clin Oncol 17 (1999) 1580], to novel molecular agents such as those involved in tumour angiogenesis [
Br J Cancer 83 (2000) P6] and antivascular therapy [
Proc Annu Meet Am Soc Clin Oncol 19 (2000) 179a]. This review will evaluate the achievements of PET in the drug development process, an approach that promises to facilitate the rapid translation of scientific research into current clinical practice. |
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ISSN: | 0959-8049 1879-0852 |
DOI: | 10.1016/S0959-8049(02)00413-6 |