4.5 Article

Paediatric atypical choroid plexus papilloma: is adjuvant therapy necessary?

期刊

JOURNAL OF NEURO-ONCOLOGY
卷 155, 期 1, 页码 63-70

出版社

SPRINGER
DOI: 10.1007/s11060-021-03843-2

关键词

Paediatric atypical choroid plexus papilloma; Choroid plexus tumour; Management; Outcomes

向作者/读者索取更多资源

Choroid plexus tumours, particularly atypical choroid plexus papillomas (aCPPs), are rare in children and there is no consensus on the optimal management approach. This study found that aCPP can be successfully managed with surgical resection alone, without the need for adjuvant therapies. Methylation profiling showed similarities between aCPPs, choroid plexus papillomas, and choroid plexus carcinomas.
Introduction Choroid Plexus Tumours (CPTs) account for 1-4% of all brain tumours in children. Atypical choroid plexus papillomas (aCPPs) are a subset of these tumours, defined over a decade ago, yet no consensus exists on the optimal approach to their management. Methods We conducted a retrospective analysis of all patients treated for CPTs at the Hospital for Sick Children between January 1, 2000, and December 31, 2018, and focused on patients with aCPP. Data extracted from the patient records for analysis included: demographic and clinical features, radiological imaging, surgical and adjuvant therapies, key pathological features, immunohistochemical staining for TP53 and tumour karyotype. Six of seven aCPP samples were profiled using Illumina HumanMethylationEPIC arrays and the top 10,000 most variably methylated probes were visualized using tSNE. Copy number inferencing was also performed. Results Twenty-nine patients were diagnosed with CPT, seven of whom had a diagnosis of aCPP as confirmed by histological review. Methylation profiling demonstrated that aCPPs clustered with both choroid plexus papillomas (CPPs) and choroid plexus carcinomas (CPCs). Complete resection of the tumour was pursued in all cases of aCPP and no patient received adjuvant therapy. All aCPP patients were alive at last follow up. Conclusions This limited case series suggests that paediatric aCPP can be successfully managed with surgical resection alone, followed by a 'watch and wait' approach thus avoiding adjuvant therapies. A deeper understanding of the biology of aCPP is required to identify objective markers which can help provide robust risk stratification and inform treatment strategies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据