TY - JOUR
T1 - Imaging of gliomas at 1.5 and 3 Tesla - A comparative study
AU - Tselikas, Lambros
AU - Souillard-Scemama, Raphaëlle
AU - Naggara, Olivier
AU - Mellerio, Charles
AU - Varlet, Pascale
AU - Dezamis, Edouard
AU - Domont, Julien
AU - Dhermain, Frédéric
AU - Devaux, Bertrand
AU - Chrétien, Fabrice
AU - Meder, Jean François
AU - Pallud, Johan
AU - Oppenheim, Catherine
N1 - Publisher Copyright:
© The Author(s) 2014. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - Background. Glioma follow-up is based on MRI parameters, which are correlated with survival. Although established criteria are used to evaluate tumor response, radiological markers may be confounded by differences in instrumentation including the magnetic field strength. We assessed whether MRIs obtained at 3 Tesla (T) and 1.5T provided similar information. Methods. We retrospectively compared imaging features of 30 consecutive patients with WHO grades II and III gliomas who underwent MRI at 1.5T and 3T within a month of each other, without any clinical changes during the same period. We compared lesion volumes on fluid attenuation inversion recovery (FLAIR), ratio of cerebral blood volume (rCBV) on perfusion-weighted imaging, contrast-to-noise ratio (CNR) on FLAIR, and on post-gadolinium 3D T1-weighted sequences between 1.5T and 3T using intraclass correlation coefficient (ICC). Concordance between observers within and between modalities was evaluated using weighted-kappa coefficient (wκ). Results. The mean±SD delay between modalities (1.5T and 3T MRI) was 8.6±5.6 days. Interobserver/intraobserver concordance for lesion volume was almost perfect for 1.5T (ICC = 0.96/0.97) and 3T (ICC = 0.99/0.98). Agreement between observers for contrast enhancement was excellent at 1.5T (wκ = 0.92) and 3T (wκ = 0.92). The tumor CNR was significantly higher for FLAIR at 1.5T (P < .001), but it was higher at 3T (P = .012) for contrast enhancement. Correlations between modalities for lesion volume (ICC = 0.97) and for rCBV values (ICC = 0.92) were almost perfect. Conclusions. In the follow-up of WHO grades II and III gliomas, 1.5T and 3T provide similar MRI features, suggesting that monitoring could be performed on either a 1.5 or a 3T MR magnet.
AB - Background. Glioma follow-up is based on MRI parameters, which are correlated with survival. Although established criteria are used to evaluate tumor response, radiological markers may be confounded by differences in instrumentation including the magnetic field strength. We assessed whether MRIs obtained at 3 Tesla (T) and 1.5T provided similar information. Methods. We retrospectively compared imaging features of 30 consecutive patients with WHO grades II and III gliomas who underwent MRI at 1.5T and 3T within a month of each other, without any clinical changes during the same period. We compared lesion volumes on fluid attenuation inversion recovery (FLAIR), ratio of cerebral blood volume (rCBV) on perfusion-weighted imaging, contrast-to-noise ratio (CNR) on FLAIR, and on post-gadolinium 3D T1-weighted sequences between 1.5T and 3T using intraclass correlation coefficient (ICC). Concordance between observers within and between modalities was evaluated using weighted-kappa coefficient (wκ). Results. The mean±SD delay between modalities (1.5T and 3T MRI) was 8.6±5.6 days. Interobserver/intraobserver concordance for lesion volume was almost perfect for 1.5T (ICC = 0.96/0.97) and 3T (ICC = 0.99/0.98). Agreement between observers for contrast enhancement was excellent at 1.5T (wκ = 0.92) and 3T (wκ = 0.92). The tumor CNR was significantly higher for FLAIR at 1.5T (P < .001), but it was higher at 3T (P = .012) for contrast enhancement. Correlations between modalities for lesion volume (ICC = 0.97) and for rCBV values (ICC = 0.92) were almost perfect. Conclusions. In the follow-up of WHO grades II and III gliomas, 1.5T and 3T provide similar MRI features, suggesting that monitoring could be performed on either a 1.5 or a 3T MR magnet.
KW - Glioma
KW - MRI
KW - Neuroimaging
KW - Observer variation
KW - Reproducibility of results
UR - http://www.scopus.com/inward/record.url?scp=84943172800&partnerID=8YFLogxK
U2 - 10.1093/neuonc/nou332
DO - 10.1093/neuonc/nou332
M3 - Article
C2 - 25526734
AN - SCOPUS:84943172800
SN - 1522-8517
VL - 17
SP - 895
EP - 900
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 6
ER -