O-(2-18F-fluoroethyl)-L-tyrosine PET predicts failure of antiangiogenic treatment in patients with recurrent high-grade glioma

J Nucl Med. 2011 Jun;52(6):856-64. doi: 10.2967/jnumed.110.086645.

Abstract

The objective of this study was to compare MRI response assessment with metabolic O-(2-(18)F-fluoroethyl)-L-tyrosine ((18)F-FET) PET response evaluation during antiangiogenic treatment in patients with recurrent high-grade glioma (rHGG).

Methods: Eleven patients with rHGG were treated biweekly with bevacizumab-irinotecan. MR images and (18)F-FET PET scans were obtained at baseline and at follow-up 8-12 wk after treatment onset. MRI treatment response was evaluated by T1/T2 volumetry according to response assessment in neurooncology (RANO) criteria. For (18)F-FET PET evaluation, an uptake reduction of more than 45% calculated with a standardized uptake value of more than 1.6 was defined as a metabolic response (receiver-operating-characteristic curve analysis). MRI and (18)F-FET PET volumetry results and response assessment were compared with each other and in relation to progression-free survival (PFS) and overall survival (OS).

Results: At follow-up, MR images showed partial response in 7 of 11 patients (64%), stable disease in 2 of 11 patients (18%), and tumor progression in 2 of 11 patients (18%). In contrast, (18)F-FET PET revealed 5 of 11 metabolic responders (46%) and 6 of 11 nonresponders (54%). MRI and (18)F-FET PET showed that responders survived significantly longer than did nonresponders (10.24 vs. 4.1 mo, P = 0.025, and 7.9 vs. 2.3 mo, P = 0.015, respectively). In 4 patients (36.4%), diagnosis according to RANO criteria and (18)F-FET PET was discordant. In these cases, PET was able to detect tumor progression earlier than was MRI.

Conclusion: In rHGG patients undergoing antiangiogenic treatment, (18)F-FET PET seems to be predictive for treatment failure in that it contributes important information to response assessment based solely on MRI and RANO criteria.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Angiogenesis Inhibitors / therapeutic use*
  • Antibodies, Monoclonal / therapeutic use
  • Antibodies, Monoclonal, Humanized
  • Astrocytoma / drug therapy
  • Astrocytoma / pathology
  • Astrocytoma / surgery
  • Bevacizumab
  • Brain Neoplasms / diagnostic imaging*
  • Brain Neoplasms / drug therapy*
  • Camptothecin / analogs & derivatives
  • Camptothecin / therapeutic use
  • Combined Modality Therapy
  • Disease-Free Survival
  • Female
  • Glioma / diagnostic imaging*
  • Glioma / drug therapy*
  • Glioma / surgery
  • Humans
  • Image Processing, Computer-Assisted
  • Irinotecan
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Nervous System Diseases / etiology
  • Nervous System Diseases / physiopathology
  • Positron-Emission Tomography
  • Postoperative Complications / physiopathology
  • Predictive Value of Tests
  • Radiopharmaceuticals*
  • Retrospective Studies
  • Survival Analysis
  • Treatment Failure
  • Tyrosine / analogs & derivatives*
  • Ultrasonography

Substances

  • Angiogenesis Inhibitors
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • O-(2-fluoroethyl)tyrosine
  • Radiopharmaceuticals
  • Bevacizumab
  • Tyrosine
  • Irinotecan
  • Camptothecin