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

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY
Amparo Saenz, Yamila Basilotta Marquez, Emma A Dalton, Romina Argañaraz, Beatriz Mantese
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引用次数: 0

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.

儿童巨大幕上脑肿瘤:功能结局和无进展生存分析。
本研究旨在确定影响手术切除的巨大幕上脑肿瘤(GSBTs)儿童患者无进展生存(PFS)的因素。第二个目的是分析这些相同的因素如何长期影响功能结果。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。对患者进行至少24个月的PFS和总生存期(OS)分析。功能状态评分(FSS)用于评估功能结局。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IV级肿瘤。24个月PFS和OS分别为51.85%和74.04%。13例患者发生pfs终止事件或治疗失败。我们发现术后FFS患者的PFS比术后FSS患者的PFS更差(HR 4.51;P = 0.03)。3次以上手术的患者比1次或2次手术的患者PFS更差(HR 11.39;P = 0.004)。高级别肿瘤的PFS比低级别肿瘤差(HR 1.55;P = 0.04)。最后,中枢神经系统感染患者的PFS比无该并发症的患者更差(HR 2.70;P = 0.04)。结论:小儿GSBTs是一种复杂的病变,需要多学科治疗。在选择最佳治疗方案时应考虑手术治疗和生活质量。影响长期PFS的因素包括组织病理学高度分级、需要三次或三次以上手术、术后FSS [gt;16]和中枢神经系统感染。
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
Pediatric Neurosurgery
Pediatric Neurosurgery 医学-临床神经学
CiteScore
1.30
自引率
0.00%
发文量
45
审稿时长
>12 weeks
期刊介绍: Articles in ''Pediatric Neurosurgery'' strives to publish new information and observations in pediatric neurosurgery and the allied fields of neurology, neuroradiology and neuropathology as they relate to the etiology of neurologic diseases and the operative care of affected patients. In addition to experimental and clinical studies, the journal presents critical reviews which provide the reader with an update on selected topics as well as case histories and reports on advances in methodology and technique. This thought-provoking focus encourages dissemination of information from neurosurgeons and neuroscientists around the world that will be of interest to clinicians and researchers concerned with pediatric, congenital, and developmental diseases of the nervous system.
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