Abstract

PurposeRecent studies have shown that tumor vascular endothelial cells and various tumor cells overexpress receptors for vascular endothelial growth factor (VEGF). The aim of this study was to investigate the prognostic value of [123I]-VEGF scintigraphy in patients with histologically verified brain tumors.Methods23 consecutive patients (9 women and 14 men aged 30–83 years, mean age 56.6 ± 14.4 years) with histopathologically-verified primary brain tumors were included in the study. All patients had undergone [123I]-VEGF scintigraphy. SPECT examinations of brain were performed 30 min and 18 h after injection. Additional [11C]-methionine PET ([11C]-MET PET) was performed in eight of the 23 patients. Both [123I]-VEGF and [11C]-MET PET were evaluated visually and semiquantitatively by tumor-to-normal brain uptake ratio (T/N ratio). Thresholds of the T/N ratio were evaluated by analysis of receiver operating characteristics (ROC). Overall survival (OS) was estimated using the Kaplan-Meier method.ResultsWorld Health Organization (WHO) grade IV glioma lesions showed [123I]-VEGF uptake 18 h after the injection, whereas other brain tumors of grade II or III showed negative results. There was no significant difference in the tumor size between VEGF positive and VEGF negative tumors. Patients with [123I]-VEGF T/N ratio threshold <1.32 showed significantly longer survival than patients with T/N ratio ≥ 1.32 (2680 days vs 295 days; P < 0.05). In the subgroup of 16 grade IV glioma patients, significant OS differences were found using a T/N ratio of 1.75 as threshold (T/N ratio < 1.75: 720 days; T/N ≥ 1.75: 183 days; P < 0.05). Significant difference (P < 0.05) was also found in [11C]-MET PET T/N ratios between the grade IV glioma (mean T/N ratio: 3.71) and the grade II or III glioma (mean T/N ratio: 1.74).ConclusionOur results suggest that [123I]-VEGF scintigraphy may be useful for visualization of tumor angiogenesis. In addition, [123I]-VEGF may provide relevant prognostic information in patients with glioma.

Highlights

  • Angiogenesis is essential for the growth of many tumors and metastases

  • vascular endothelial growth factor (VEGF) binds to VEGF receptor 1 (VEGFR1, Fms-like-tyrosine kinase (Flt-1)) and VEGFR2 (kinase domain region (KDR), Flk-1), which may activate endothelial cell proliferation, migration and survival [3, 4]

  • Based on our previous studies [16,17,18], in this prospective study we evaluated for the first time the prognostic role of [123I] - vascular endothelial growth factor ([123I]-VEGF) in patients with histologically confirmed brain tumors

Read more

Summary

Introduction

Recent studies have demonstrated that human glioblastoma (World Health Organization (WHO) grade IV glioma) overexpresses proangiogenic factors, including vascular endothelial growth factor (VEGF) [1, 2]. Previous studies demonstrated that VEGF and its corresponding receptor Flk-1 are significant prognostic factors for overall survival in patients with glioma [6, 7]. A recent imaging study assessing tumor uptake of a radiolabeled anti-VEGF antibody, such as the monoclonal antibody bevacizumab in glioma, showed unsatisfactory results with significant inter- and intra-patient heterogeneity [13]. Based on our previous studies [16,17,18], in this prospective study we evaluated for the first time the prognostic role of [123I] - vascular endothelial growth factor ([123I]-VEGF) in patients with histologically confirmed brain tumors

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call