17–20 May 2015
La Biodola, Isola d'Elba
Europe/Rome timezone

Congruency of Tumour Volume Delineated by FET PET and MRSI

19 May 2015, 11:40
15m
Room Maria Luisa

Room Maria Luisa

Talk 6 - Whole-body and dedicated organ MR-PET Session 6 - Whole-body and dedicated organ MR-PET

Speaker

Jörg Mauler (Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany)

Description

In addition to MR imaging, PET imaging of O-(2-[18F]Fluorethyl)-L-Tyrosine (FET) uptake provides information on brain tumour extent and metabolic activity [1]. Similarly, MRS has been shown to be of value for distinguishing high- from low-grade gliomas [2]. Based on 2D spatially resolved MRSI, an overlap between 18FET uptake and the choline/N-acetyl-aspartate (Cho/NAA) ratio of more than 75 % has been reported [3]. Aim: To measure spatial correlation of 18FET-PET with 3D spatially resolved MRSI in patients with gliomas. Methods: 14 patients (46±16 y) with gliomas (WHO grade II-IV) were examined by simultaneous 18FET-PET-3D-MRSI measurements which covered the whole brain (Siemens BrainPET/3T MR TIM Trio; MRSI: EPSI sequence [4], TE=17.6 ms). The data were analysed with respect to the congruency of the suspicious tissue delineated by the FET uptake and the Cho/NAA ratio. Locations of individual maxima and distances in between were determined. The congruency of the tumour was assessed using Dice’s coefficients for assumed same tumour volume. All comparisons were carried out at the spatial resolution of the whole brain spectroscopic image (64x64x32 vxl, 5.6x5.6x10mm3 each). Results: The intensity maxima of both modalities were (61±51) mm distant from each other. The average level of congruency between the tumour volumes delineated in the FET uptake and MRSI data was (33±25)%. Discussion – Conclusion: Metabolically active tumour tissue, as depicted by FET uptake, is represented to a low extent by the choline/N-acetyl-aspartate ratio measured by spatially resolved 3D MRSI, which is in contrast to previous findings [3]. Both modalities may reflect independent physiological properties of gliomas. [1] Pauleit, Brain 128. [2] Zeng,Magn Reson Imag 29. [3] Stadlbauer, J Nucl Med 49. [4] Ebel, MRM 53.

Primary author

Jörg Mauler (Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany)

Co-authors

Prof. Andrew Arthur Maudsley (Miller School of Medicine, University of Miami, Miami, FL, USA) Dr Christian Filss (Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany) Dr Gabriele Stoffels (Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany) Prof. Karl-Josef Langen (Institute of Neuroscience and Medicine, Forschungszentrum Jülich, Jülich, Germany) Prof. N. Jon Shah (Institute of Neuroscience and Medicine - 4, Forschungszentrum Juelich) Dr Omid Nikoubashman (Department of Neuroradiology, Faculty of Medicine, RWTH Aachen University, Aachen, Germany)

Presentation materials