Diagnostic accuracy of MRI without gadolinium for follow-up of pilocytic astrocytoma in the paediatric population

IF 1.8 4区 医学 Q3 CLINICAL NEUROLOGY Journal of Clinical Neuroscience Pub Date : 2025-05-01 Epub Date: 2025-03-13 DOI:10.1016/j.jocn.2025.111173
Macfarlane Adam Ian , Soares Jewel Hannah , Maharaj Monish
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Abstract

Purpose

Pilocytic astrocytoma is the most common glial tumour in the paediatric population with a long-term life expectancy after surgery. Long-term radiological follow-up with magnetic resonance imaging (MRI) is necessary to detect recurrence of tumour or growth of residual tumour. Established MRI protocols typically dictate post-gadolinium sequences despite concerns around the side-effect and safety concerns of gadolinium-based contrast agents. This study aims to investigate whether omission of gadolinium-enhanced sequences for the long term follow-up MRI for paediatric patients with pilocytic astrocytoma, maintains diagnostic accuracy assessing potential recurrence or growth of residual tumour.

Methods

A retrospective review of follow-up MRI for 47 patients with histopathologically proven pilocytic astrocytoma was performed. Patients with optic pathway or suprasellar glioma were excluded from this study. All patients underwent surgery and had a minimum of 2 years of postoperative imaging for review. MRIs were chosen from most recent report of stability or at a time when growth/progression had been diagnosed. Two neuroradiologists and two paediatric neurosurgeons were randomly allocated a series of MRIs with gadolinium enhanced sequences removed, reviewers were blinded to the original report and subsequent treatment decisions. In addition, 30 paired MRI studies were randomly allocated to second review to test interobserver reliability. The reviewer responses were recorded and compared with the original report and analysed with respect to preserved diagnostic accuracy.

Results

170 MRI scans were subject to review across 66 episodes of care for 47 patients. 22.7 % of patients experienced growth of residual tumour during the period of follow-up. The sensitivity of non-enhanced MRI for detection of growth was 82 % (95 %CI 64.40–92.12) with a specificity of 97.10 % (95 % CI 90.03–99.20). Accuracy was similar for both neuroradiologists and neurosurgeons (91.49 % vs. 94 %). Interobserver reliability was calculated using Cohen’s Kappa co-efficient with a result of 0.792 showing substantial agreement. We also confirmed a statistically significant difference between gross total resection and sub-total resection and correlation with future growth (41 % vs. 0 %, n = 64, p = 0.001).

Conclusion

In paediatric patients who have undergone surgery for pilocytic astrocytoma, long term MRI follow-up without gadolinium-enhanced sequences maintains diagnostic accuracy compared with enhanced sequences. Omission of gadolinium-enhanced sequences may lead to decreased costs, duration of scans and anxiety around follow-up procedures.
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无钆MRI对儿童毛细胞星形细胞瘤随访的诊断准确性
目的:毛囊细胞星形细胞瘤是儿科人群中最常见的神经胶质肿瘤,术后寿命长。长期的放射学随访与磁共振成像(MRI)是必要的,以发现肿瘤复发或残余肿瘤的生长。尽管考虑到钆基造影剂的副作用和安全性问题,现有的MRI方案通常要求钆后序列。本研究旨在探讨在儿童毛细胞星形细胞瘤患者的长期随访MRI检查中,遗漏钆增强序列是否能保持诊断的准确性,以评估潜在的复发或残留肿瘤的生长。方法回顾性分析47例经组织病理学证实的毛细胞星形细胞瘤的MRI随访资料。视神经通路或鞍上胶质瘤患者被排除在本研究之外。所有患者均接受手术,术后至少2年影像学检查。mri是从最近的稳定性报告中选择的,或者是在诊断出生长/进展的时候。两名神经放射科医生和两名儿科神经外科医生被随机分配了一系列去除钆增强序列的mri,评论者对原始报告和随后的治疗决定不知情。此外,30个成对的MRI研究被随机分配到第二次回顾,以测试观察者之间的可靠性。记录审稿人的回答,并与原始报告进行比较,并分析保留的诊断准确性。结果对47例患者66次护理中的170次MRI扫描进行了回顾。22.7%的患者在随访期间出现肿瘤残留生长。非增强MRI检测肿瘤生长的敏感性为82% (95% CI 64.40 ~ 92.12),特异性为97.10% (95% CI 90.03 ~ 99.20)。神经放射学家和神经外科医生的准确率相似(91.49%对94%)。使用科恩Kappa系数计算观察者间的信度,结果为0.792,显示出实质性的一致。我们还证实了总全切除和次全切除之间的统计学显著差异以及与未来生长的相关性(41%对0%,n = 64, p = 0.001)。结论在接受毛细胞星形细胞瘤手术的儿童患者中,与增强序列相比,不加钆增强序列的长期MRI随访保持诊断准确性。遗漏钆增强序列可能导致成本降低、扫描时间延长和后续程序的焦虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Neuroscience
Journal of Clinical Neuroscience 医学-临床神经学
CiteScore
4.50
自引率
0.00%
发文量
402
审稿时长
40 days
期刊介绍: This International journal, Journal of Clinical Neuroscience, publishes articles on clinical neurosurgery and neurology and the related neurosciences such as neuro-pathology, neuro-radiology, neuro-ophthalmology and neuro-physiology. The journal has a broad International perspective, and emphasises the advances occurring in Asia, the Pacific Rim region, Europe and North America. The Journal acts as a focus for publication of major clinical and laboratory research, as well as publishing solicited manuscripts on specific subjects from experts, case reports and other information of interest to clinicians working in the clinical neurosciences.
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