TY - JOUR
T1 - Quantification of serial changes in cerebral blood volume and metabolism in patients with recurrent glioblastoma undergoing antiangiogenic therapy
AU - Stadlbauer, Andreas
AU - Pichler, Petra
AU - Karl, Marianne
AU - Brandner, Sebastian
AU - Lerch, Claudia
AU - Renner, Bertold
AU - Heinz, Gertraud
N1 - Publisher Copyright:
© 2015 Elsevier Ireland Ltd.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - OBJECTIVES: To evaluate the usefulness of quantitative advanced magnetic resonance imaging (MRI) methods for assessment of antiangiogenic therapy (AAT) response in recurrent glioblastoma multiforme (GBM).METHODS: Eighteen patients with recurrent GBM received bevacizumab and 18 patients served as control group. Baseline MRI and two follow-up examinations were acquired every 3-5 months using dynamic susceptibility-weighted contrast (DSC) perfusion MRI and (1)H-MR spectroscopic imaging ((1)H-MRSI). Maps of absolute cerebral blood volume (aCBV) were coregistered with choline (Cho) and N-acetyl-aspartate (NAA) concentrations and compared to usually used relative parameters as well as controls.RESULTS: Perfusion significantly decreased in responding and pseudoresponding GBMs but also in normal appearing brain after AAT onset. Cho and NAA concentrations were superior to Cr-ratios in lesion differentiation and showed a clear gap between responding and pseudoresponding lesions. Responders to AAT exceptionally frequently (6 out of 8 patients) showed remote GBM progression.CONCLUSIONS: Quantification of CBV reveals changes in normal brain perfusion due to AAT, which were not described so far. DSC perfusion MRI seems not to be suitable for differentiation between response and pseudoresponse to AAT. However, absolute quantification of brain metabolites may allow for distinction due to a clear gap at 6-9 months after therapy onset.
AB - OBJECTIVES: To evaluate the usefulness of quantitative advanced magnetic resonance imaging (MRI) methods for assessment of antiangiogenic therapy (AAT) response in recurrent glioblastoma multiforme (GBM).METHODS: Eighteen patients with recurrent GBM received bevacizumab and 18 patients served as control group. Baseline MRI and two follow-up examinations were acquired every 3-5 months using dynamic susceptibility-weighted contrast (DSC) perfusion MRI and (1)H-MR spectroscopic imaging ((1)H-MRSI). Maps of absolute cerebral blood volume (aCBV) were coregistered with choline (Cho) and N-acetyl-aspartate (NAA) concentrations and compared to usually used relative parameters as well as controls.RESULTS: Perfusion significantly decreased in responding and pseudoresponding GBMs but also in normal appearing brain after AAT onset. Cho and NAA concentrations were superior to Cr-ratios in lesion differentiation and showed a clear gap between responding and pseudoresponding lesions. Responders to AAT exceptionally frequently (6 out of 8 patients) showed remote GBM progression.CONCLUSIONS: Quantification of CBV reveals changes in normal brain perfusion due to AAT, which were not described so far. DSC perfusion MRI seems not to be suitable for differentiation between response and pseudoresponse to AAT. However, absolute quantification of brain metabolites may allow for distinction due to a clear gap at 6-9 months after therapy onset.
KW - Angiogenesis Inhibitors/therapeutic use
KW - Aspartic Acid/analogs & derivatives
KW - Bevacizumab/therapeutic use
KW - Blood Volume/drug effects
KW - Brain/blood supply
KW - Brain Mapping
KW - Brain Neoplasms/blood supply
KW - Cerebrovascular Circulation/drug effects
KW - Choline/metabolism
KW - Contrast Media/therapeutic use
KW - Female
KW - Follow-Up Studies
KW - Glioblastoma/blood supply
KW - Humans
KW - Magnetic Resonance Angiography
KW - Magnetic Resonance Imaging/methods
KW - Magnetic Resonance Spectroscopy/methods
KW - Male
KW - Middle Aged
KW - Neoplasm Recurrence, Local/blood supply
KW - Reproducibility of Results
UR - http://www.scopus.com/inward/record.url?scp=84929023141&partnerID=8YFLogxK
U2 - 10.1016/j.ejrad.2015.02.025
DO - 10.1016/j.ejrad.2015.02.025
M3 - Journal article
C2 - 25795194
SN - 0720-048X
VL - 84
SP - 1128
EP - 1136
JO - European Journal of Radiology
JF - European Journal of Radiology
IS - 6
ER -