Skip to main content
. 2020 May 29;10(6):357. doi: 10.3390/diagnostics10060357

Table 1.

Summary of the studies included in the review.

Authors Year Study Design Number of Patients Tumor Histotype/ Glioma Grade PET Scanner Type MRI Technique Main Findings
Diagnosis and Differential Diagnosis
Valentini et al. [20] 2017 R 12
(48 biopsy specimens)
GBM PET/CT DWI,
DTI,
DSC-PWI,
MRSI
Highest values of rCBV, Cho/Cr, Cho/NAA, proportional decrease of SUVmax with increasing distance from the CE region.
At histological examination, the CE region showed maximum tumor histological malignancy and presented the maximum values of rCBV, Cho/Cr, Cho/NAA, LL and SUVmax.
Yamashita et al. [47] 2016 R 50 GBM = 33
PCNSL = 17
PET/CT DWI,
IVIM
Significantly higher fmax (p < 0.001) and Dmin (p < 0.0001) and significantly lower SUVmax (p < 0.0005) in GBM than in PCNSL.
Nakajima et al. [38] 2015 R 34 GBM = 23
PCNSL = 11
PET/CT DWI,
DSC-PWI
High SS (100%) and SP (73.9%) of 18F-FDG PET in differentiating GBM from PCNSL. Good accuracy of ADC5% and uncorr
Grading
Shaw et al. [44] 2019 R 33 36 histology samples:
II = 11
III = 17
IV = 4 metastases = 1 benign = 3
PET/CT Gd MRI Combination of PET and MRI imaging enhances AC in identifying high-grade regions of glioma.
PET: SS = 59%, SP = 79%, PPV = 89%, NPV = 55%.
MRI: SS = 77%, SP = 86%, PPV = 89%, NPV = 71%.
Combined PET and MRI: SS = 79%, SP = 100%, PPV = 100%, NPV = 75%.
Sakata et al. [41] 2018 R 49 II = 15
III-IV = 34
PET/CT DWI, APT Comparable AC of T/N and ADCmin and amide proton transfer in the discrimination of HGGs from LGGs. A larger increase for the diagnosis of HGGs with the combination APT + T/N compared to ADCmin + T/N.
Takano et al. [46] 2016 R 35 II = 23
III = 12
PET/CT DTI, DWI No satisfactory performance for average fractional anisotropy, and maximum fractional anisotropy, minimum ADC, T/Nmax and T/Nave in discriminating III from II grade.
Song et al. [45] 2016 R 70 LGG and HGG PET/CT Gd MRI 18F-FDG PET/CT performs better (in terms of SS, SP and AC) than MRI (p < 0.05) for identifying different grades of glioma.
Sacconi et al. [40] 2016 R 20 II = 6
III = 3
IV = 6
metastases = 2 meningioma = 2 lymphoma = 1
PET/MR PWI Utility of rCBVmean and SUVmean in discriminating HGGs from LGGS. rCBVmean (optimal cut-off value = 1.74): SS = 100%, SP = 74%.
SUVmean, (optimal cut-off value = 4.0): SS = 50%, SP = 79.5%.
Prognosis
Lundemann et al. [37] 2019 P 16 GBM PET/CT (18F-FET)
PET/MR (18F-FDG)
DWI,
DCE
18F-FDG and 18F-FET uptake demonstrate the highest mutual correlation in CELs and NELs, with 18F-FET being the most important to predict recurrence. Fractional anisotropy resulted in the second most important parameter for recurrence probability in apparently healthy tissue.
Chiang et al. [29] 2017 R 44 GBM PET/CT ADC Metabolic tumor volume and tumor cross products on 18F-FDG PET and on MRI may serve as prognostic variables. Combining the cross products of both PET and MRI, the AC in predicting poor survival increased to 74% from 58% using MRI alone.
Leiva-Salinas et al. [36] 2017 R 56 GBM PET/CT Gd MRI SUVr may be a useful imaging marker to identify patients’ decreased survival after standard therapy.
SUVr was not influenced by tumor size and location on MRI images at diagnosis.
Assessment of Recurrence
Seligman et al. [42] 2019 R 41 III = 21
IV = 20
PET/MRI DCE 18F-FDG PET and DCE-MRI hold comparable AC (80% vs. 83%) in identifying tumor recurrence.
Hojjati et al. [32] 2018 R 24 (28 lesions) GBM PET/MRI
PET/CT
DCE, DSC-PWI, DWI The authors documented an AUC of 1.0 in a joint predictive model including r-mean ≥ 1.31 and a CBV ≥ 3.32.
By contrast, a model encompassing only CBV ≥ 3.32 demonstrated a lower AUC (0.94).
Arora et al. [27] 2018 P 29 LGG = 15, HGG = 14 PET/CT Gd MRI On per-patient analysis, no significance difference was found between the performance of 18F-FDG PET/CT and MRI (AC = 82.8% vs. 76.6%) in detecting recurrence. MRI did not detect significantly more lesions than 18F-FDG PET/CT (p = 0.14).
Jena et al. [35] 2017 R 35 II = 9
III = 13
IV = 19
PET/MR DWI, PWI, MRS PET provides complementary information to MRI. The AUC obtained combining MRI metrics (rCBV, mean ADC, Cho/Cr) and the PET parameter (mean T/N) was higher (0.935 ± 0.046) than the curve that resulted only from the three MRI parameters (0.913 ± 0.053).
Hatzoglou et al. [30] 2016 P 29 II = 7
III = 8
IV = 18
PET/CT DCE The combination of a plasma volume ratio ≥ 2.1 and a SUVratio ≥ 1.2 improve the performance in distinguishing progression from radiation injury compared to individual PET and DCE metrics.
Sharma et al. [43] 2016 R 64 Low-grade astrocytoma = 22
High-grade astrocytoma = 16
Medulloblastoma = 10
Other miscellaneous brain tumors = 6
PET/CT NR Good performance of PET and MRI in detecting recurrence in oligodendroglioma.
In low-grade astrocytomas, a high rate of false positive cases (10/22 patients) were documented for PET. Nevertheless, PET was helpful in all cases reported as equivocal (n = 5) by MRI.
Iagaru et al. [33] 2015 P 17 GBM PET/CT Gd MRI Similar diagnostic performance of the two modalities for recurrent GBM (13/15 detected recurrences for PET vs. 14/15 MR).
Treatment Planning and Evaluation of Response to Therapy
Idegushi et al. [34] 2018 P 16 II = 8
III = 8
PET/CT Gd MRI, T2-w, FLAIR 18F-FDG PET may also help in planning surgical resection. Only partial overlap between 18F-FDG uptake and the contrast-enhancement area. Tissue extracted from the 18F-FDG and Gd MRI positive areas presented anaplastic features. Tissue extracted from 18F-FDG and Gd MRI negative areas resulted in grade II glioma at pathological examination.
Hirata et al. [31] 2019 P 25 III = 10
IV = 15
PET Gd MRI, T2-w Tumor delineation is underestimated by Gd MRI. High overlap of DS and T1-Gd positively influenced survival.
Back et al. [28] 2017 P 10 III PET/CT T1-w, Gd MRI, T2-w 18F-FDG PET guided integrated boost intensity-modulated RT (b-IMRT) that may result in a reduced dose to the normal brain when compared to standard IMRT (s-IMRT).
O’Neill et al. [39] 2016 P 12 III PET/CT DCE, DWI The MRI-derived metrics (ADCmean, Ktrans, Ve) demonstrated significant variation in the patients (median difference of Ktrans = −41.8%, p < 0.02, median difference of Ve = −42.6%, p < 0.04), possibly reflecting the early effects of VEGF trap on tumour vasculature. No systematic changes were observed for SUVmax (median difference = −7.8%, p > 0.67).

R: retrospective; P: prospective; N: number; GBM: glioblastoma multiforme; DWI: diffusion-weighted imaging; DSC-PWI: dynamic susceptibility-contrast perfusion-weighted imaging; MRSI: MR spectroscopic imaging; CBV: cerebral blood volume; Cho/Cr: Choline/Creatine; Cho/NAA: Choline/N-acetylaspartate; LL: Lipids/Lactate; IVIM: intravoxel incoherent motion; f: perfusion fraction; D: diffusion coefficient; SS: sensitivity; SP: specificity; AC: accuracy; ADC: apparent diffusion coefficient; Gd: gadolinium; DTI: diffusion tensor imaging; CE: contrast-enhancing; CEL: contrast-enhancing lesion; NE: non-enhancing; NEL: non-enhancing lesion; APT: amide proton transfer; T/N: tumor-to-normal tissue ratio; SUVr: standardized uptake value ratio (calculated as the SUVmax in the tumor relative to that in healthy white matter); AUC: area under the curve; r-mean: SUVmean of the lesion/ SUVmean of the contralateral background; FLAIR: Fluid Attenuated Inversion Recovery; T1-w: T1-weighted; T2-w: T2-weighted; DS: decoupling score (magnitude of the disrupted correlation of 11C-methionine and 18F-FDG, reflecting glioma cell invasion); Ktrans: transfer constant; Ve: extravascular extracellular volume fraction; VEGF: vascular endothelial growth factor; VEGF Trap: a soluble recombinant decoy receptor inactivating extravascular and circulating VEGF); NR: not reported.