Prognostic factors of thalamic and thalamopeduncular low-grade gliomas in children: A systematic review and recommendations for surgical management

IF 1.9 Q3 CLINICAL NEUROLOGY
Jana Táborská , Adéla Bubeníková , Petr Skalický , Jakub Táborský , David Horváth , Michal Zápotocký , Ondřej Bradáč , Vladimír Beneš 3rd
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引用次数: 0

Abstract

Introduction

Pediatric low-grade gliomas arising from the thalamus or thalamopeduncular junction are rare. Prognostic factors are thus seldom reported in the literature.

Research question

This systematic review aims to define the factors influencing the prognosis of pediatric patients with thalamic and thalamopeduncular low-grade gliomas.

Material and methods

An extensive literature search in adherence to Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines was performed and included Web of Science, Scopus, and OVID interface (Medline and Embase). Original articles were selected if they provided data on 10 or more patients under 18 years old with separate or retrievable data for thalamic or thalamopeduncular low-grade gliomas, as well as at least one prognostic factor and its corresponding outcome. The risk of bias and applicability were assessed using The Quality Assessment of Prognostic Accuracy Studies criteria.

Results

The study selection process resulted in the inclusion of 14 articles out of the initial pool of 876 references. These 14 articles encompassed data from 446 patients. The prognostic factors reported were the extent of resection in ten studies, age and radiotherapy in four studies, bilateral involvement and molecular genetics in two studies, and sex and dissemination in one study each. Significant prognostic factors included the extent of resection, bilateral involvement, histology, and radiotherapy.

Discussion and conclusion

The reported factors considered significant for prognosis align with previously published data. The maximal safe resection, as a potentially curative modality for thalamic low-grade glioma, and the multidisciplinary approach to each patient should be a standard of care. Given the excellent long-term outlook of these patients, the extent of resection should not be pursued at the risk of neurological function since additional therapeutic possibilities are available today, such as molecular-targeted agents.
小儿低度神经胶质瘤起源于丘脑或丘脑髓核交界处是罕见的。因此,预后因素在文献中很少报道。本系统综述旨在探讨影响丘脑及丘脑核低级别胶质瘤患儿预后的因素。材料和方法根据系统评价和荟萃分析指南的首选报告项目进行了广泛的文献检索,包括Web of Science, Scopus和OVID接口(Medline和Embase)。如果提供了10名或更多18岁以下患者的资料,并有单独或可检索的丘脑或丘脑管低级别胶质瘤的资料,以及至少一个预后因素及其相应的结果,则选择原创文章。使用预后准确性研究质量评估标准评估偏倚风险和适用性。结果在研究选择过程中,876篇初始参考文献中有14篇被纳入。这14篇文章包含了来自446名患者的数据。报告的预后因素是10项研究的切除程度,4项研究的年龄和放疗,2项研究的双侧受累和分子遗传学,以及各一项研究的性别和传播。重要的预后因素包括切除程度、双侧受累、组织学和放疗。讨论和结论报道的影响预后的重要因素与先前发表的数据一致。最大限度的安全切除,作为丘脑低级别胶质瘤的潜在治疗方式,以及对每个患者的多学科方法应该是一个标准的护理。考虑到这些患者良好的长期前景,切除的程度不应该以神经功能的风险为代价,因为目前有其他治疗方法,如分子靶向药物。
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
Brain & spine
Brain & spine Surgery
CiteScore
1.10
自引率
0.00%
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0
审稿时长
71 days
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