Literature DB >> 11355142

Positron emission tomography with 2-[18F]-fluoro-2-deoxy-D-glucose in oncology. Part IIIb: Therapy response monitoring in colorectal and lung tumours, head and neck cancer, hepatocellular carcinoma and sarcoma.

M P Stokkel1, A Draisma, E K Pauwels.   

Abstract

Positron emission tomography (PET) using 18F-fluorodeoxyglucose (FDG) is considered to be a very useful adjunct to anatomic imaging techniques and is now primarily used for oncological indications. These indications include diagnosis, staging, and therapy monitoring. In this review, we discuss the articles in which FDG-PET is clinically used for monitoring therapy in lung and colorectal tumours, head and neck cancer, sarcoma, and hepatocellular carcinoma. It is found that the amount of FDG uptake strongly correlates with response to therapy: a decrease in FDG uptake after therapy indicates a positive response to therapy. However, this conclusion is based on small numbers of patients, whereas the exact response mechanism is still unknown. Moreover, in these case series, the interval between tumour therapy and FDG-PET, as well as the method of quantification, SUV or tumour-to-non-tumour ratios, differ per study. Finally, dynamic imaging is a recommended technique by some authors, but it is not a standard technique in clinical practice to evaluate tumour therapy. Therefore, further study is required which has to deal with these major issues before it is possible to draw definite conclusions.

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Year:  2001        PMID: 11355142     DOI: 10.1007/s004320000208

Source DB:  PubMed          Journal:  J Cancer Res Clin Oncol        ISSN: 0171-5216            Impact factor:   4.553


  11 in total

1.  [PET/CT in radiotherapy].

Authors:  M Weckesser; S Könemann; M Brinkmann; N Willich; O Schober
Journal:  Radiologe       Date:  2004-11       Impact factor: 0.635

2.  18F-Fluorodeoxyglucose uptake on positron emission tomography/computed tomography is associated with metastasis and epithelial-mesenchymal transition in hepatocellular carcinoma.

Authors:  Misu Lee; Jeong Yong Jeon; Micheal L Neugent; Jung-Whan Kim; Mijin Yun
Journal:  Clin Exp Metastasis       Date:  2017-04-20       Impact factor: 5.150

3.  Targeting glucose metabolism in cancer: new class of agents for loco-regional and systemic therapy of liver cancer and beyond?

Authors:  Lynn Jeanette Savic; Julius Chapiro; Gregor Duwe; Jean-François Geschwind
Journal:  Hepat Oncol       Date:  2016-01-01

Review 4.  Critical issues in response evaluation on computed tomography: lessons from the gastrointestinal stromal tumor model.

Authors:  Haesun Choi
Journal:  Curr Oncol Rep       Date:  2005-07       Impact factor: 5.075

5.  Comparison of different SUV-based methods for monitoring cytotoxic therapy with FDG PET.

Authors:  A Stahl; K Ott; M Schwaiger; W A Weber
Journal:  Eur J Nucl Med Mol Imaging       Date:  2004-07-15       Impact factor: 9.236

Review 6.  Methodology for quantitative rapid multi-tracer PET tumor characterizations.

Authors:  Dan J Kadrmas; John M Hoffman
Journal:  Theranostics       Date:  2013-10-04       Impact factor: 11.556

Review 7.  Metabolic Portraits of Breast Cancer by HR MAS MR Spectroscopy of Intact Tissue Samples.

Authors:  Tonje H Haukaas; Leslie R Euceda; Guro F Giskeødegård; Tone F Bathen
Journal:  Metabolites       Date:  2017-05-16

8.  Change of Apoptosis and Glucose Metabolism in Lung Cancer Xenografts during Cytotoxic and Anti-Angiogenic Therapy Assessed by Annexin V Based Optical Imaging and 18F-FDG-PET/CT.

Authors:  Jasmin Gross; Karin Palmowski; Dennis Doleschel; Anne Rix; Felix Gremse; Frederic Verburg; Felix M Mottaghy; Fabian Kiessling; Wiltrud Lederle; Moritz Palmowski
Journal:  Contrast Media Mol Imaging       Date:  2021-04-10       Impact factor: 3.161

9.  Early detection of recurrence by 18FDG-PET in the follow-up of patients with colorectal cancer.

Authors:  I Sobhani; E Tiret; R Lebtahi; T Aparicio; E Itti; F Montravers; C Vaylet; P Rougier; T André; J M Gornet; D Cherqui; C Delbaldo; Y Panis; J N Talbot; M Meignan; D Le Guludec
Journal:  Br J Cancer       Date:  2008-02-26       Impact factor: 7.640

Review 10.  Cancer Metabolism as a Mechanism of Treatment Resistance and Potential Therapeutic Target in Hepatocellular Carcinoma.

Authors:  Misu Lee; Haeyong Ko; Mijin Yun
Journal:  Yonsei Med J       Date:  2018-12       Impact factor: 2.759

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