Head-to-head comparison of [18F]-mFBG versus [123I]-MIBG in neuroblastoma: a systematic review and meta-analysis.

IF 2.5 3区 医学 Q2 PEDIATRICS
Pediatric Radiology Pub Date : 2026-10-01 Epub Date: 2026-07-08 DOI:10.1007/s00247-026-06713-z
Domenico Albano, Francesco Bertagna, Arnoldo Piccardo, Francesco Fiz, Giorgio Treglia
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引用次数: 0

Abstract

Hybrid imaging is fundamental in the staging and response assessment of patients affected by neuroblastoma (NB). [123I]-metaiodobenzylguanidine (MIBG) scintigraphy±single-photon emission computed tomography/computed tomography (SPECT/CT) is considered the gold standard for the evaluation of NB, but it presents some limitations, such as the time-consuming procedure (2 days), the low spatial resolution, and challenging interpretation. Alternative positron emission tomography/computed tomography (PET/CT) catecholaminergic radiopharmaceuticals have been investigated to overtake the issues of [123I]-MIBG. Among them, one of the most promising seems to be meta-[18F]fluorobenzylguanidine ([18F]-mFBG). Thus, we planned a head-to-head systematic review and meta-analysis to compare [18F]-mFBG PET/CT and [123I]-MIBG SPECT/CT in NB. We executed a literature search to identify all articles performing a head-to-head comparison between these two methods, excluding review articles, preclinical studies, case reports, and small case series (less than 5 patients). Finally, five studies were collected for a total of 115 patients and 1,644 lesions. A patients-based analysis showed that [18F]-mFBG PET/CT had a higher pooled sensitivity than [123I]-MIBG SPECT/CT (97% vs 82%, respectively) and identical pooled specificity (82%). Also at a lesion-based analysis, [18F]-mFBG PET/CT demonstrated better sensitivity (99% vs 51.5%). In conclusion, preliminary evidence-based data demonstrate that [18F]-mFBG PET/CT showed superior diagnostic performance than [123I]-MIBG SPECT/CT. However, it is still unclear the real added value of [18F]-mFBG PET/CT compared to [123I]-MIBG SPECT/CT in the change of clinical management. These findings suggest [18F]-mFBG PET/CT may become a superior, more efficient alternative to [123I]-MIBG for staging and response assessment in neuroblastoma. Future studies should focus on its impact on clinical management and patient outcomes.

[18F]-mFBG与[123I]-MIBG在神经母细胞瘤中的正面比较:系统回顾和荟萃分析
混合成像是神经母细胞瘤(NB)患者分期和反应评估的基础。[123I]-metaiodobenzylguanidine (MIBG)闪烁成像±单光子发射计算机断层扫描/计算机断层扫描(SPECT/CT)被认为是评估NB的金标准,但它存在一些局限性,例如耗时(2天)、低空间分辨率和具有挑战性的解释。替代正电子发射断层扫描/计算机断层扫描(PET/CT)儿茶酚胺能放射性药物已被研究以取代[123I]-MIBG的问题。其中,最有希望的一种似乎是间[18F]氟苯基胍([18F]- mfbg)。因此,我们计划对[18F]-mFBG PET/CT和[123I]-MIBG SPECT/CT在NB中的对比进行系统回顾和荟萃分析。我们进行了文献检索,以确定所有在这两种方法之间进行正面比较的文章,不包括综述文章、临床前研究、病例报告和小病例系列(少于5例患者)。最后,我们收集了5项研究,共涉及115例患者和1,644个病变。一项基于患者的分析显示,[18F]-mFBG PET/CT的综合敏感性高于[123I]-MIBG SPECT/CT(分别为97%和82%),两者的综合特异性相同(82%)。同样在基于病变的分析中,[18F]-mFBG PET/CT显示出更好的灵敏度(99% vs 51.5%)。总之,初步的循证数据表明[18F]-mFBG PET/CT的诊断性能优于[123I]-MIBG SPECT/CT。然而,[18F]-mFBG PET/CT与[123I]-MIBG SPECT/CT在临床管理改变中的真正附加价值尚不清楚。这些发现表明[18F]-mFBG PET/CT可能成为神经母细胞瘤分期和疗效评估的更好、更有效的替代方法[123I]-MIBG。未来的研究应关注其对临床管理和患者预后的影响。
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来源期刊
Pediatric Radiology
Pediatric Radiology 医学-核医学
CiteScore
4.40
自引率
17.40%
发文量
300
审稿时长
3-6 weeks
期刊介绍: Official Journal of the European Society of Pediatric Radiology, the Society for Pediatric Radiology and the Asian and Oceanic Society for Pediatric Radiology Pediatric Radiology informs its readers of new findings and progress in all areas of pediatric imaging and in related fields. This is achieved by a blend of original papers, complemented by reviews that set out the present state of knowledge in a particular area of the specialty or summarize specific topics in which discussion has led to clear conclusions. Advances in technology, methodology, apparatus and auxiliary equipment are presented, and modifications of standard techniques are described. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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