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| Hauptseite > Publikationsdatenbank > Role of O-(2-18 F-Fluoroethyl)-L-Tyrosine PET for differentiation of local recurrent brain metastasis from radiation necrosis |
| Hauptseite > Publikationsdatenbank > Role of O-(2-18 F-Fluoroethyl)-L-Tyrosine PET for differentiation of local recurrent brain metastasis from radiation necrosis |
| Journal Article | PreJuSER-22779 |
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2012
Society of Nuclear Medicine
New York, NY
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Please use a persistent id in citations: doi:10.2967/jnumed.112.103325
Abstract: The aim of this study was to investigate the potential of O-(2-(18)F-fluoroethyl)-L-tyrosine ((18)F-FET) PET for differentiating local recurrent brain metastasis from radiation necrosis after radiation therapy because the use of contrast-enhanced MRI for this issue is often difficult.Thirty-one patients (mean age ± SD, 53 ± 11 y) with single or multiple contrast-enhancing brain lesions (n = 40) on MRI after radiation therapy of brain metastases were investigated with dynamic (18)F-FET PET. Maximum and mean tumor-to-brain ratios (TBR(max) and TBR(mean), respectively; 20-40 min after injection) of (18)F-FET uptake were determined. Time-activity curves were generated, and the time to peak (TTP) was calculated. Furthermore, time-activity curves of each lesion were assigned to one of the following curve patterns: (I) constantly increasing (18)F-FET uptake, (II) (18)F-FET uptake peaking early (TTP ≤ 20 min) followed by a plateau, and (III) (18)F-FET uptake peaking early (TTP ≤ 20 min) followed by a constant descent. The diagnostic accuracy of the TBR(max) and TBR(mean) of (18)F-FET uptake and the curve patterns for the correct identification of recurrent brain metastasis were evaluated by receiver-operating-characteristic analyses or Fisher exact test for 2 × 2 contingency tables using subsequent histologic analysis (11 lesions in 11 patients) or clinical course and MRI findings (29 lesions in 20 patients) as reference.Both TBR(max) and TBR(mean) were significantly higher in patients with recurrent metastasis (n = 19) than in patients with radiation necrosis (n = 21) (TBR(max), 3.2 ± 0.9 vs. 2.3 ± 0.5, P < 0.001; TBR(mean), 2.1 ± 0.4 vs. 1.8 ± 0.2, P < 0.001). The diagnostic accuracy of (18)F-FET PET for the correct identification of recurrent brain metastases reached 78% using TBR(max) (area under the ROC curve [AUC], 0.822 ± 0.07; sensitivity, 79%; specificity, 76%; cutoff, 2.55; P = 0.001), 83% using TBR(mean) (AUC, 0.851 ± 0.07; sensitivity, 74%; specificity, 90%; cutoff, 1.95; P < 0.001), and 92% for curve patterns II and III versus curve pattern I (sensitivity, 84%; specificity, 100%; P < 0.0001). The highest accuracy (93%) to diagnose local recurrent metastasis was obtained when both a TBR(mean) greater than 1.9 and curve pattern II or III were present (AUC, 0.959 ± 0.03; sensitivity, 95%; specificity, 91%; P < 0.001).Our findings suggest that the combined evaluation of the TBR(mean) of (18)F-FET uptake and the pattern of the time-activity curve can differentiate local brain metastasis recurrence from radionecrosis with high accuracy. (18)F-FET PET may thus contribute significantly to the management of patients with brain metastases.
Keyword(s): Adolescent (MeSH) ; Adult (MeSH) ; Aged (MeSH) ; Biological Transport (MeSH) ; Brain Neoplasms: metabolism (MeSH) ; Brain Neoplasms: radionuclide imaging (MeSH) ; Brain Neoplasms: secondary (MeSH) ; Diagnosis, Differential (MeSH) ; Humans (MeSH) ; Male (MeSH) ; Middle Aged (MeSH) ; Necrosis: metabolism (MeSH) ; Necrosis: radionuclide imaging (MeSH) ; Neoplasm Recurrence, Local: metabolism (MeSH) ; Neoplasm Recurrence, Local: radionuclide imaging (MeSH) ; Positron-Emission Tomography (MeSH) ; ROC Curve (MeSH) ; Radiation Injuries: metabolism (MeSH) ; Radiation Injuries: radionuclide imaging (MeSH) ; Tyrosine: analogs & derivatives (MeSH) ; Tyrosine: diagnostic use (MeSH) ; Tyrosine: metabolism (MeSH) ; Young Adult (MeSH) ; O-(2-fluoroethyl)tyrosine ; Tyrosine ; J ; radiation necrosis (auto) ; stereotactic radiosurgery (auto) ; recurrent brain metastasis (auto) ; amino acid PET (auto) ; F-18-fluoroethyl-L-tyrosine (F-18-FET) (auto)
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