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使用 18F-FDOPA PET 对神经母细胞瘤进行特征分析。

Characterization of neuroblastic tumors using 18F-FDOPA PET.

机构信息

Department of Pediatrics, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

J Nucl Med. 2013 Jan;54(1):42-9. doi: 10.2967/jnumed.112.102772. Epub 2012 Dec 4.

Abstract

UNLABELLED

Neuroblastic tumors are childhood neoplasms that possess amino acid decarboxylase (AADC) activity and can theoretically be imaged by (18)F-fluorodihydroxyphenylalanine ((18)F-FDOPA) PET, a new diagnostic tool for neuroendocrine tumors. In this study, we explored the accuracy and clinical role of (18)F-FDOPA PET in neuroblastic tumors.

METHODS

From 2008 to 2011, patients with tissue-proven neuroblastic tumors receiving (18)F-FDOPA PET at initial diagnosis or during follow-ups were enrolled. The sensitivity and specificity of (18)F-FDOPA PET were compared with those of (123)I-metaiodobenzylguanidine ((123)I-MIBG) scintigraphy and (18)F-FDG PET, using tumor histology as the standard. The maximum standardized uptake value and tumor-to-liver uptake ratio on (18)F-FDOPA PET were measured and correlated with AADC messenger RNA level in tumor tissue.

RESULTS

Fifty tumors from 34 patients, including 42 neuroblastic tumors and 8 lesions without viable tumor cells, were eligible for analysis. (18)F-FDOPA PET successfully detected neuroblastic tumors of different histologic types in various anatomic sites, at a sensitivity of 97.6% (87.4%-99.9%) and a specificity of 87.5% (47.3%-99.7%). In tumors with concomitant studies, (18)F-FDOPA PET demonstrated a higher sensitivity than (123)I-MIBG scintigraphy (n = 18; P = 0.0455) or (18)F-FDG PET (n = 46; P = 0.0455). Among the 18 tumors with concomitant (123)I-MIBG scans, 4 tumors with viable cells were (123)I-MIBG-negative but were successfully detected by (18)F-FDOPA PET. The tumor uptake of (18)F-FDOPA significantly correlated with AADC expression (n = 15 nonhepatic tumors; maximum standardized uptake value, P = 0.0002; tumor-to-liver uptake ratio, P < 0.0001).

CONCLUSION

(18)F-FDOPA PET showed high sensitivity and specificity in detecting and tracking neuroblastic tumors in this preliminary study with a small cohort of patients and might be complementary to (123)I-MIBG scintigraphy and (18)F-FDG PET. By correlating with AADC expression, (18)F-FDOPA PET might serve as a useful imaging tool for the functional assessment of neuroblastic tumors.

摘要

目的

从 2008 年至 2011 年,我们招募了经组织学证实的神经母细胞瘤患者,这些患者在初始诊断或随访期间接受了(18)F-氟多巴(18)F-FDOPA PET 检查。以肿瘤组织学为标准,比较(18)F-FDOPA PET 与(123)I-间位碘代苄胍(123)I-MIBG 闪烁扫描和(18)F-FDG PET 的敏感性和特异性。测量(18)F-FDOPA PET 上的最大标准化摄取值和肿瘤与肝脏摄取比,并与肿瘤组织中的 AADC 信使 RNA 水平相关。

结果

34 例患者的 50 个肿瘤,包括 42 个神经母细胞瘤和 8 个无存活肿瘤细胞的病变,符合分析标准。(18)F-FDOPA PET 成功检测到不同组织学类型的神经母细胞瘤,在各种解剖部位的敏感性为 97.6%(87.4%-99.9%),特异性为 87.5%(47.3%-99.7%)。在伴有研究的肿瘤中,(18)F-FDOPA PET 比(123)I-MIBG 闪烁扫描(n = 18;P = 0.0455)或(18)F-FDG PET(n = 46;P = 0.0455)的敏感性更高。在伴有(123)I-MIBG 扫描的 18 个肿瘤中,4 个有存活细胞的肿瘤(123)I-MIBG 阴性,但(18)F-FDOPA PET 成功检测到。(18)F-FDOPA 的肿瘤摄取与 AADC 表达显著相关(n = 15 个非肝肿瘤;最大标准化摄取值,P = 0.0002;肿瘤与肝脏摄取比,P < 0.0001)。

结论

在这项初步研究中,(18)F-FDOPA PET 显示出在检测和跟踪神经母细胞瘤方面的高敏感性和特异性,该研究纳入了一小部分患者,并且可能与(123)I-MIBG 闪烁扫描和(18)F-FDG PET 互补。通过与 AADC 表达相关,(18)F-FDOPA PET 可能成为评估神经母细胞瘤功能的有用成像工具。

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