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- 18F-fluoroethyl)-L-tyrosine (18F-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 18F-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 18F-FET PET, a decision tree model was used. Effectiveness of 18F-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 18F-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 18F-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 costeffectiveness ratio of 18F-FET PET/MR imaging compared with MR imaging alone was V5,725 (ε1 ≈ $1.30) for the baseline scenario and V8,145 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 18F-FET PET in the management of patients with recurrent high-grade glioma treated with BEV/IR may be cost-effective. Integration of 18F-FET PET has the potential to avoid overtreatment and corresponding costs, as well as unnecessary side effects to the patient. COPYRIGHT © 2013 by the Society of Nuclear Medicine and Molecular Imaging, Inc.
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Heinzel, A., Müller, D., Langen, K. J., Blaum, M., Verburg, F. A., Mottaghy, F. M., & Galldiks, N. (2013). 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. Journal of Nuclear Medicine, 54(8), 1217–1222. https://doi.org/10.2967/jnumed.113.120089
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