Molecular imaging of pediatric brain tumors: comparison of tumor metabolism using ¹⁸F-FDG-PET and MRSI.
Molecular imaging of pediatric brain tumors: comparison of tumor metabolism using ¹⁸F-FDG-PET and MRSI.
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DOI:
10.1007/s11060-012-0918-0
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发表时间:
2012-09
影响因子:
3.9
通讯作者:
Warren, Katherine E.
中科院分区:
文献类型:
--
作者:
Hipp, Sean J.;Steffen-Smith, Emilie A.;Patronas, Nicholas;Herscovitch, Peter;Solomon, Jeffrey M.;Bent, Robyn S.;Steinberg, Seth M.;Warren, Katherine E.
Magnetic resonance spectroscopic imaging (MRSI) and 18F-Fluorodeoxyglucose positron emission tomography (FDG-PET) are non-invasive imaging techniques routinely used to evaluate tumor malignancy in adults with brain tumors. We compared the metabolic activity of pediatric brain tumors using FDG-PET and MRSI. Children (n=37) diagnosed with a primary brain tumor underwent FDG-PET and MRSI within two weeks of each other. Tumor metabolism was classified as inactive, active or highly active using the maximum choline:N-acetyl-asparate (Cho:NAA) on MRSI and the highest tumor uptake on FDG-PET. A voxel-wise comparison was used to evaluate the area with the greatest abnormal metabolism. Agreement between methods was assessed using the percent agreement and the kappa statistic (κ). Pediatric brain tumors were metabolically heterogeneous on FDG-PET and MRSI studies. Active tumor metabolism was observed more frequently using MRSI compared to FDG-PET, and agreement in tumor classification was weak (κ=0.16, p=0.12), with 42% agreement (95% CI= 25 – 61%). Voxel-wise comparison for identifying the area of greatest metabolic activity showed overlap in the majority (62%) of studies, though exact agreement between techniques was low (29.4%, 95% CI = 15.1 – 47.5%). These results indicate that FDG-PET and MRSI detect similar but not always identical regions of tumor activity, and there is little agreement in the degree of tumor metabolic activity between the two techniques.
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影响因子:
6.2
作者:
Tzika, AA;Astrakas, LG;Black, PM
通讯作者:
Black, PM
影响因子:
4.8
作者:
Verma, Ragini;Zacharaki, Evangelia I.;Ou, Yangming;Cai, Hongmin;Chawla, Sanjeev;Lee, Seung-Koo;Melhem, Elias R.;Wolf, Ronald;Davatzikos, Christos
通讯作者:
Davatzikos, Christos
影响因子:
2.3
作者:
Horská A;Barker PB
通讯作者:
Barker PB
影响因子:
6.2
作者:
Utriainen, M;Metsähonkala, L;Minn, H
通讯作者:
Minn, H
影响因子:
11.5
作者:
Astrakas, LG;Zurakowski, D;Black, PM
通讯作者:
Black, PM