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儿童巨大幕上脑肿瘤:功能预后和无进展生存分析。

Giant Supratentorial Brain Tumors in Children: Functional Outcome and Progression-Free Survival Analysis.

机构信息

Pediatric Neurosurgery Department, Pediatric Hospital Prof. Dr. Juan P. Garrahan, Buenos Aires, Argentina.

Neurosurgery Department, The National Hospital for Neurology and Neurosurgery, Queen Square, London, UK.

出版信息

Pediatr Neurosurg. 2023;58(3):117-127. doi: 10.1159/000530592. Epub 2023 Apr 10.

Abstract

INTRODUCTION

This study aimed to identify factors affecting progression-free survival (PFS) in pediatric patients with giant supratentorial brain tumors (GSBTs) treated with surgical excision. The secondary aim was to analyze how these same factors affected the functional outcome in the long term.

METHODS

We performed a retrospective, analytical, single-center cohort study. We included all pediatric patients with GSBT between January 2014 and June 2018. Patients were followed for a minimum of 24 months for the PFS and overall survival (OS) analysis. Functional status score (FSS) was used to assess the functional outcome.

RESULTS

We included 27 patients with GSBT, the median age was six (range 2-12), and eleven patients had a grade IV tumor. The 24-month PFS and OS were 51.85% and 74.04%, respectively. A PFS-ending event or treatment failure occurred in 13 patients. We found that patients with postoperative FFS >16 have a worse PFS than patients with a postoperative FSS <15 (HR 4.51; p = 0.03). Patients with more than three surgeries had worse PFS than patients with one or two procedures (HR 11.39; p = 0.004). High-grade tumors were associated with worse PFS than low-grade tumors (HR 1.55; p = 0.04). Finally, patients with CNS infections had worse PFS than patients without that complication (HR 2.70; p = 0.04).

CONCLUSIONS

GSBTs in pediatric patients are complex lesions that require multidisciplinary management. Surgical management and quality of life should be considered when choosing the best treatment. Factors influencing long-term PFS were high-grade histopathology, the need for three or more surgeries, postoperative FSS >16, and CNS infections.

摘要

引言

本研究旨在确定影响接受手术切除的儿童大型幕上脑肿瘤(GSBT)患者无进展生存期(PFS)的因素。次要目的是分析这些相同因素如何影响长期的功能结果。

方法

我们进行了一项回顾性、分析性、单中心队列研究。我们纳入了 2014 年 1 月至 2018 年 6 月期间所有患有 GSBT 的儿科患者。对 PFS 和总生存期(OS)分析进行了至少 24 个月的随访。功能状态评分(FSS)用于评估功能结果。

结果

我们纳入了 27 例 GSBT 患者,中位年龄为 6 岁(范围 2-12 岁),11 例患者为 4 级肿瘤。24 个月的 PFS 和 OS 分别为 51.85%和 74.04%。13 例患者出现 PFS 终点事件或治疗失败。我们发现术后 FFS >16 的患者 PFS 比术后 FSS <15 的患者更差(HR 4.51;p = 0.03)。接受三次以上手术的患者比接受一两次手术的患者 PFS 更差(HR 11.39;p = 0.004)。高级别肿瘤与较低级别肿瘤相比 PFS 更差(HR 1.55;p = 0.04)。最后,患有中枢神经系统感染的患者 PFS 比无该并发症的患者更差(HR 2.70;p = 0.04)。

结论

儿童 GSBT 是复杂的病变,需要多学科管理。在选择最佳治疗方法时,应考虑手术管理和生活质量。影响长期 PFS 的因素包括高级别组织病理学、需要三次或更多次手术、术后 FSS >16 和中枢神经系统感染。

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