首页> 美国卫生研究院文献>Neuro-Oncology >NI-19THE USE OF DYNAMIC O-(2-18Ffluoroethyl)-L-TYROSINE-PET IN THE CLINICAL EVALUATION OF BRAIN TUMORS IN CHILDREN AND ADOLESCENTS
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NI-19THE USE OF DYNAMIC O-(2-18Ffluoroethyl)-L-TYROSINE-PET IN THE CLINICAL EVALUATION OF BRAIN TUMORS IN CHILDREN AND ADOLESCENTS

机译:NI-19动态O-(2- 18F氟乙基)-L-酪氨酸-PET在儿童和青少年脑肿瘤临床评估中的应用

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摘要

BACKGROUND: Experience regarding the use of dynamic O-(2-[18F]-fluoroethyl)-L-tyrosine (18F-FET) PET in children and adolescents with brain tumors is limited. METHODS: Sixty-nine 18F-FET PET scans of 49 patients (median age, 13 years; range, 1-18 years) were analyzed retrospectively. Patients had been referred for: (A) assessment of newly diagnosed cerebral lesions (26 scans in 26 patients), (B) diagnosing tumor progression/recurrence (24 scans in 18 patients), (C) monitoring of chemotherapy effects (8 scans in 4 patients), and (D) the detection of residual tumor tissue after resection (11 scans in 10 patients). Maximum and mean tumor/brain ratios (TBRmax/mean) of 18F-FET uptake were determined (20-40 min p.i.) and time-activity curves were generated and assigned to one of the following patterns: (1) constantly increasing uptake, (2) uptake peaking at a midway point (>20-40 min) followed by a plateau, and (3) uptake peaking early (≤20 min) followed by a constant descent. The diagnostic values of TBRs and kinetic parameters to detect neoplastic tissue or diagnose tumor progression/recurrence were assessed using ROC analyses. Diagnoses were confirmed histologically and/or by clinical course. RESULTS: In patients with newly diagnosed cerebral lesions, highest accuracy (77%) to detect neoplastic tissue (7 of 26 patients) was obtained when TBRmax was >1.7 (AUC, 0.80 ± 0.09; sensitivity, 79%; specificity, 71%, PPV, 88%; P = 0.02). For diagnosing tumor progression/recurrence, highest accuracy (82%) was obtained when curve patterns 2 or 3 were present (AUC, 0.80 ± 0.11; sensitivity, 75%; specificity, 90%, PPV, 90%; P = 0.02). During chemotherapy, a decrease of TBRs was associated with a stable clinical course at least for 6 months. In patients after complete tumor resection (2 of 10 patients), 18F-FET PET detected metabolically active tumor (TBRmax ≥ 1.7). CONCLUSIONS: Our findings suggest that 18F-FET PET can add valuable information for clinical decision-making in pediatric brain tumor patients.
机译:背景:在患有以下疾病的儿童和青少年中使用动态O-(2-[ 18 F]-氟乙基)-L-酪氨酸( 18 F-FET)PET的经验脑肿瘤是有限的。方法:回顾性分析49例患者的69例 18 F-FET PET扫描(中位年龄13岁;范围1-18岁)。已为患者提供以下服务:(A)评估新诊断的脑部病变(26例患者中有26例扫描),(B)诊断肿瘤的进展/复发(18例中有24例),(C)监测化学疗法的效果(8例扫描中) (4名患者),以及(D)切除后检测残余肿瘤组织(10名患者进行11次扫描)。确定(spi> 18 F-FET摄取的最大和平均肿瘤/大脑比(TBRmax /平均值)(20-40分钟pi),并生成时间活动曲线并将其分配给以下模式之一: (1)不断增加摄取,(2)摄取在中点(> 20-40分钟)达到峰值,然后达到平稳,(3)摄取达到峰值(≤20min)早期,然后持续下降。使用ROC分析评估TBR的诊断价值和动力学参数以检测赘生性组织或诊断肿瘤进展/复发。通过组织学和/或临床过程确诊。结果:在新诊断出的脑部病变患者中,当TBRmax> 1.7(AUC,0.80±0.09;敏感性,79%;特异性,71%,≥71)时,检测肿瘤组织的准确性最高(77%)。 PPV,88%; P = 0.02)。对于诊断肿瘤进展/复发,当出现曲线图2或3时,可获得最高准确度(82%)(AUC,0.80±0.11;灵敏度,75%;特异性,90%,PPV,90%; P = 0.02)。在化疗期间,TBR的减少与至少6个月的稳定临床过程相关。在完全切除肿瘤的患者中(10名患者中有2名), 18 F-FET PET检测到代谢活跃的肿瘤(TBRmax≥1.7)。结论:我们的研究结果表明, 18 F-FET PET可以为小儿脑肿瘤患者的临床决策提供有价值的信息。

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