Prognostic value of <sup>18</sup>F-FET PET imaging in re-irradiation of high-grade glioma: Results of a phase I clinical trial.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 27622554.
- Also identified by DOI 10.1016/j.radonc.2016.08.014.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Positron emission tomography (PET) provides quantitative metabolic information and potential biomarkers of treatment outcome. We aimed to determine the prognostic value of early <sup>18</sup>F-fluoroethyl-tyrosine (<sup>18</sup>F-FET) PET scans acquired during re-irradiation for recurrent high-grade glioma (HGG). A phase I clinical trial of re-irradiation of HGG was carried out. MRI and <sup>18</sup>F-FET PET were used for target delineation and follow-up. Images were acquired at baseline, during radiotherapy and 4weeks post-treatment and compared by measuring the metabolically active biological tumor volume (BTV) and maximal activity (T<sub>max</sub>/B). Correlations with outcomes were assessed by multivariate Cox regression analysis. Thirty-one patients were included and all patients have died. The median overall survival was 7.0 mos. Both baseline BTV and baseline MRI volume (necrotic/cystic cavities subtracted) were prognostic for overall survival (OS) in multivariate analysis (HR=1.3 p<0.01 and HR=1.3 p<0.01, respectively). Early changes in BTV and T<sub>max</sub>/B were observed but they carried no independent prognostic information. Baseline biological tumor volume (BTV) defined by <sup>18</sup>F-FET PET was prognostic for OS in multivariate analysis, as was MRI volume (necrotic/cystic cavities subtracted). Tumor volume may aid in identifying patients whose life expectancy is too short to warrant re-irradiation.
Medical subject headings
- Brain Neoplasms
- Glioma
- Radiopharmaceuticals
- Tyrosine