The use of O-(2-18F-fluoroethyl)-L-tyrosine PET for treatment management of bevacizumab and irinotecan in patients with recurrent high-grade glioma: a cost-effectiveness analysis

J Nucl Med. 2013 Aug;54(8):1217-22. doi: 10.2967/jnumed.113.120089. Epub 2013 Jun 19.

Abstract

To date, the use of structural MR imaging (including contrast-enhanced and T2-weighted or fluid-attenuated inversion recovery-weighted images) is the standard method to diagnose tumor progression and to assess antiangiogenic treatment effects. However, several studies have suggested that O-(2-(18)F-fluoroethyl)-L-tyrosine ((18)F-FET) PET adds valuable clinical information to the information derived from structural MR imaging alone. We evaluated the effectiveness and cost-effectiveness of the addition of (18)F-FET PET to structural MR imaging for the management of treatment with bevacizumab and irinotecan (BEV/IR) in patients with recurrent high-grade glioma compared with MR imaging alone from the perspective of the German Statutory Health Insurance.

Methods: To evaluate the incremental cost-effectiveness of the additional use of (18)F-FET PET, a decision tree model was used. Effectiveness of (18)F-FET PET was defined as correct identification of both tumor progression before BEV/IR treatment initiation and BEV/IR treatment response and was evaluated for the combination of (18)F-FET PET and MR imaging compared with MR imaging alone. Costs were estimated for a baseline scenario and for a more expensive scenario. The robustness of the results was tested using deterministic and probabilistic sensitivity analyses.

Results: The use of (18)F-FET PET resulted in a number needed to diagnose of 2.4, that is, 3 additional patients have to be diagnosed to avoid 1 wrong diagnosis. The incremental cost-effectiveness ratio of (18)F-FET PET/MR imaging compared with MR imaging alone was €5,725 (€1 ≈ $1.30) for the baseline scenario and €8,145 for the more expensive scenario per additional correct diagnosis. The probabilistic sensitivity analysis confirmed the robustness of the results.

Conclusion: The model suggests that the additional use of (18)F-FET PET in the management of patients with recurrent high-grade glioma treated with BEV/IR may be cost-effective. Integration of (18)F-FET PET has the potential to avoid overtreatment and corresponding costs, as well as unnecessary side effects to the patient.

Keywords: 18F-FET PET; cost-effectiveness analysis; decision tree model; recurrent glioma.

MeSH terms

  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Bevacizumab
  • Brain Neoplasms / diagnostic imaging*
  • Brain Neoplasms / drug therapy
  • Brain Neoplasms / pathology
  • Camptothecin / analogs & derivatives*
  • Camptothecin / therapeutic use
  • Cost-Benefit Analysis
  • Decision Trees*
  • Disease-Free Survival
  • Glioma / diagnostic imaging*
  • Glioma / drug therapy
  • Glioma / pathology
  • Humans
  • Irinotecan
  • Magnetic Resonance Imaging
  • Monte Carlo Method
  • Neoplasm Grading
  • Positron-Emission Tomography / economics*
  • Recurrence
  • Treatment Outcome
  • Tyrosine / analogs & derivatives*

Substances

  • Antibodies, Monoclonal, Humanized
  • (18F)fluoroethyltyrosine
  • Bevacizumab
  • Tyrosine
  • Irinotecan
  • Camptothecin