Prediction of glioma recurrence using dynamic 18F-fluoroethyltyrosine PET

T. Pyka, J. Gempt, F. Ringel, S. Hüttinger, S. Van Marwick, S. Nekolla, H. J. Wester, M. Schwaiger, S. Förster

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

20 Zitate (Scopus)

Abstract

MATERIALS AND METHODS: Thirty-four consecutive patients with untreated, first-diagnosed, histologically proved glioma were included in this retrospective study. All patients underwent dynamic PET scans before surgery (±standard treatment) and were followed up clinically and by MR imaging. Static and dynamic tumor-to-background ratio, TTP, and slope-to-peak were obtained and correlated with progression-free survival.

BACKGROUND AND PURPOSE: Inter-and intratumor heterogeneity and the variable course of disease in patients with glioma motivate the investigation of new prognostic factors to optimize individual treatment. Here we explore the usefulness of standard static and more sophisticated dynamic 18F-fluoroethyltyrosine-PET imaging for the assessment of patient prognosis.

CONCLUSIONS: 18F-fluoroethyltyrosine-PET can predict recurrence in patients with glioma, with dynamic analysis showing advantages over static imaging, especially in the low-grade subgroup.

RESULTS: Twenty of 34 patients experienced progression, with a median progression-free survival of 28.0±11.1 months. Dynamic TTP was highly prognostic for recurrent disease, showing a strong correlation with progression-free survival (hazard ratio, 6.050; 95% CI, 2.11-17.37; P < .001). Most interesting, this correlation also proved significant in the subgroup of low-grade glioma (hazard ratio, 5.347; 95% CI, 1.05-27.20; P = .044), but not when using established static imaging parameters, such as maximum tumor-to-background ratio and mean tumor-to-background ratio. In the high-grade glioma subgroup, both dynamic and static parameters correlated with progression-free survival. The best results were achieved by defining ROIs around "hot spots" in earlier timeframes, underlining the concept of intratumor heterogeneity.

OriginalspracheEnglisch
Seiten (von - bis)1924-1929
Seitenumfang6
FachzeitschriftAmerican Journal of Neuroradiology
Jahrgang35
Ausgabenummer10
DOIs
PublikationsstatusVeröffentlicht - 1 Okt. 2014

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