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First intraindividual comparison of contrast-enhanced MRI, FET- and DOTATOC- PET in patients with intracranial meningiomas.

Authors :
Dittmar JO
Kratochwil C
Dittmar A
Welzel T
Habermehl D
Rieken S
Giesel FL
Haberkorn U
Debus J
Combs SE
Source :
Radiation oncology (London, England) [Radiat Oncol] 2017 Nov 06; Vol. 12 (1), pp. 169. Date of Electronic Publication: 2017 Nov 06.
Publication Year :
2017

Abstract

Background: For irradiation treatment planning of meningiomas the use of PET-scans is well established. The most frequently used tracers are either based on amino acids or the somatostatin receptor ligand DOTATOC. Since up to now no inter-institutionally accepted standard PET-tracer has been defined, the aim of this study was to evaluate the influence of these different types of PET-tracers on the GTV-definition.<br />Methods: Twenty-one patients suffering from intracranial meningiomas underwent CT, MRI, FET- and DOTATOC-PET. First, tumour extension was delineated after image-fusion of CT and MRI (GTV <subscript>CT/MRI</subscript> ). Then distinct GTVs based either on FET- or DOTATOC-PET were contoured and compared with each other as well with GTV <subscript>CT/MRI</subscript> .<br />Results: Every tumour showed typical enhancement of DOTATOC, but two meningiomas remained FET-negative. The mean relative overlap volume of GTV <subscript>FET</subscript> and GTV <subscript>DOTATOC</subscript> was only 41.9% and there was a significantly stronger correlation between GTV <subscript>CT/MRI</subscript> and GTV <subscript>DOTATOC</subscript> than between GTV <subscript>CT/MRI</subscript> and GTV <subscript>FET</subscript> .<br />Conclusions: Further investigations are necessary to clarify the minor conformity of DOTATOC- and FET-PET in meningiomas. Because of the receptor targeting, DOTATOC is known to be more specific for meningiomas and will remain the standard in our institution with the known limitation in areas nearby the pituitary gland.

Details

Language :
English
ISSN :
1748-717X
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Radiation oncology (London, England)
Publication Type :
Academic Journal
Accession number :
29110720
Full Text :
https://doi.org/10.1186/s13014-017-0913-x