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Published in: European Journal of Nuclear Medicine and Molecular Imaging 1/2006

01-07-2006

Monitoring chemotherapy and radiotherapy of solid tumors

Authors: Wolfgang A. Weber, Hinrich Wieder

Published in: European Journal of Nuclear Medicine and Molecular Imaging | Special Issue 1/2006

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Abstract

PET imaging with the glucose analog fluorodeoxyglucose (FDG-PET) has been evaluated in numerous studies to monitor tumor response in patients undergoing chemo- and radiotherapy. The clinical value of FDG-PET for differentiation of residual or recurrent viable tumor and therapy-induced fibrosis or scar tissue has been documented for various solid tumors. Furthermore, there are now several reports suggesting that quantitative assessment of therapy-induced changes in tumor FDG uptake may allow prediction of tumor response and patient outcome very early in the course of therapy. In nonresponding patients, treatment may be adjusted according to the individual chemo- and radiosensitivity of the tumor tissue. Since the number of alternative treatments for solid tumors (e.g., second-line chemotherapy agents, protein kinase, or angiogenesis inhibitors) is continuously increasing, early prediction of tumor response to chemotherapy and radiotherapy by FDG-PET has enormous potential to “personalize” treatment and to reduce the side-effects and costs of ineffective therapy.
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Metadata
Title
Monitoring chemotherapy and radiotherapy of solid tumors
Authors
Wolfgang A. Weber
Hinrich Wieder
Publication date
01-07-2006
Publisher
Springer-Verlag
Published in
European Journal of Nuclear Medicine and Molecular Imaging / Issue Special Issue 1/2006
Print ISSN: 1619-7070
Electronic ISSN: 1619-7089
DOI
https://doi.org/10.1007/s00259-006-0133-3

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