scholarly journals Towards standardization of 18F-FET PET imaging: do we need a consistent method of background activity assessment?

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Marcus Unterrainer ◽  
Franziska Vettermann ◽  
Matthias Brendel ◽  
Adrien Holzgreve ◽  
Michael Lifschitz ◽  
...  
2009 ◽  
Vol 54 (18) ◽  
pp. 5525-5539 ◽  
Author(s):  
Frank Thiele ◽  
Julia Ehmer ◽  
Marc D Piroth ◽  
Michael J Eble ◽  
Heinz H Coenen ◽  
...  

2019 ◽  
Vol 44 (10) ◽  
pp. e581-e582 ◽  
Author(s):  
Norbert Galldiks ◽  
Anna Brunn ◽  
Gereon R. Fink ◽  
Karl-Josef Langen

2008 ◽  
Vol 35 (6Part5) ◽  
pp. 2673-2673
Author(s):  
T Chang ◽  
T Pan ◽  
G Chang ◽  
J Clark ◽  
O Mawlawi

2013 ◽  
Vol 109 (3) ◽  
pp. 487-492 ◽  
Author(s):  
Stefan Rieken ◽  
Daniel Habermehl ◽  
Frederik L. Giesel ◽  
Christoph Hoffmann ◽  
Ute Burger ◽  
...  

2012 ◽  
Vol 14 (12) ◽  
pp. 1473-1480 ◽  
Author(s):  
N. L. Jansen ◽  
C. Schwartz ◽  
V. Graute ◽  
S. Eigenbrod ◽  
J. Lutz ◽  
...  
Keyword(s):  
Fet Pet ◽  

2015 ◽  
Vol 84 (6) ◽  
pp. 1790-1797 ◽  
Author(s):  
Jens Gempt ◽  
Stefanie Bette ◽  
Niels Buchmann ◽  
Yu-Mi Ryang ◽  
Annette Förschler ◽  
...  

2019 ◽  
Vol 21 (Supplement_6) ◽  
pp. vi162-vi162 ◽  
Author(s):  
Norbert Galldiks ◽  
Jan-Michael Werner ◽  
Gabriele Stoffels ◽  
Martin Kocher ◽  
Caroline Tscherpel ◽  
...  

Abstract BACKGROUND The purpose of this study was (i) to assess the reproducibility of the previously described T2-FLAIR mismatch sign as a highly specific MR imaging marker in non-enhancing IDH-mutant, 1p/19q non-codeleted lower-grade gliomas (LGG) of the WHO grades II or III, and (ii) its association with the uptake of the radiolabeled amino acid O-(2-[18F]-fluoroethyl)-L-tyrosine (FET) in PET to further metabolically characterize that sign, which is currently poorly understood. METHODS Consecutive MRI and dynamic FET PET scans (n=134) from newly diagnosed and neuropathologically confirmed IDH-mutant LGG (n=65) and IDH-wildtype gliomas as control group (n=69) were evaluated by two independent raters to assess presence/absence of the T2-FLAIR mismatch sign as well as FET uptake. Interrater agreement was assessed using Cohen’s kappa (κ), as well as diagnostic performance (i.e., positive/negative predictive value; PPV, NPV) of the T2-FLAIR mismatch sign to identify IDH-mutant astrocytomas. RESULTS In the LGG group, 13 patients (20%) had a T2-FLAIR mismatch sign, which could be identified with a substantial interrater agreement (κ=0.75). In contrast, that sign was absent in IDH-wildtype gliomas. All 13 cases that were positive for the T2/FLAIR mismatch sign were IDH-mutant, 1p/19q non-codeleted tumors (PPV=100%, NPV=57%). Interestingly, compared to IDH-mutant gliomas without the T2-FLAIR mismatch sign, the sign was significantly (P=0.027; 10 of 13 patients) associated with a negative FET PET scan (i.e., 5 tumors with indifferent FET uptake comparable to the background activity, or FET uptake below background activity (photopenic defect) in 5 tumors). CONCLUSIONS With a robust interrater agreement, our findings are in line with previously reported findings regarding the T2-FLAIR mismatch sign. Additionally, the T2-FLAIR mismatch sign seems to be significantly related with a lack of increased FET uptake in PET, which may help to further characterize patients with that sign. Notwithstanding, the clinical relevance of this imaging constellation warrants further investigation.


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