激光间质热疗法、开放手术切除和mTOR抑制剂治疗室管膜下巨细胞星形细胞瘤的临床疗效比较

IF 0.9 4区 医学 Q4 CLINICAL NEUROLOGY Pediatric Neurosurgery Pub Date : 2023-01-01 DOI:10.1159/000531210
Scott Boop, David Bonda, Stephanie Randle, Sarah Leary, Nicholas Vitanza, Erin Crotty, Edward Novotny, Seth Friedman, Richard G Ellenbogen, Sharon Durfy, Hannah Goldstein, Jeffrey G Ojemann, Jason S Hauptman
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引用次数: 0

摘要

简介:室管膜下巨细胞星形细胞瘤(SEGA)是结节性硬化症(TSC)患者中最常见的中枢神经系统肿瘤。虽然这些是良性的,但它们靠近门罗孔经常引起梗阻性脑积水,这是一种潜在的致命并发症。开放手术切除是治疗的主要方法;然而,这可能会导致严重的发病率。mTOR抑制剂的发展改变了治疗前景,但它们的使用也有局限性。激光间质热疗法(LITT)是一种新兴的治疗方式,在治疗包括SEGAs在内的各种颅内病变方面显示出希望。我们提出了一项单一机构的回顾性研究,对采用LITT、开放切除、mTOR抑制剂或这些方式的组合治疗SEGAs的患者进行了研究。主要研究结果是最近随访时的肿瘤体积与治疗开始时的肿瘤体积的比较。次要结果是与治疗方式相关的临床并发症。方法:回顾性分析2010年至2021年在我院治疗的SEGAs患者。从医疗记录中收集人口统计、治疗信息和并发症。肿瘤体积是根据治疗开始时和最近随访时获得的影像计算的。采用Kruskal-Wallis非参数检验评估两组间肿瘤体积和随访时间的差异。结果:4例患者行LITT(3例仅行LITT), 3例行开放手术切除,4例仅行mTOR抑制剂治疗。两组平均肿瘤体积缩小率分别为48.6±13.8%、90.7±39.8%和67.1±17.2%。三组间肿瘤体积缩小率比较无统计学差异(p = 0.0513)。两组随访时间差异无统计学意义(p = 0.223)。在我们的研究中,只有1例患者需要永久性脑脊液转移,4例患者由于成本或副作用而停止或减少mTOR抑制剂的剂量。结论:我们的研究表明,LITT可以被认为是SEGAs的一种治疗选择,因为它可以有效地减少肿瘤体积,而且并发症很少。这种方式比开放切除侵入性小,对于不适合mTOR抑制剂的患者可能是另一种选择。我们推荐一种更新的SEGA治疗范例,在考虑患者特定因素后,在选定的病例中包括LITT。
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A Comparison of Clinical Outcomes for Subependymal Giant Cell Astrocytomas Treated with Laser Interstitial Thermal Therapy, Open Surgical Resection, and mTOR Inhibitors.

Introduction: Subependymal giant cell astrocytoma (SEGA) is the most common CNS tumor in patients with tuberous sclerosis complex (TSC). Although these are benign, their proximity to the foramen of Monroe frequently causes obstructive hydrocephalus, a potentially fatal complication. Open surgical resection has been the mainstay of treatment; however, this can cause significant morbidity. The development of mTOR inhibitors has changed the treatment landscape, but there are limitations to their use. Laser interstitial thermal therapy (LITT) is an emerging treatment modality that has shown promise in treatment of a variety of intracranial lesions, including SEGAs. We present a single institution, retrospective study of patients treated for SEGAs with LITT, open resection, mTOR inhibitors, or a combination of these modalities. The primary study outcome was tumor volume at most recent follow-up compared with volume at treatment initiation. The secondary outcome was clinical complications associated with treatment modality.

Methods: Retrospective chart review was performed to identify patients with SEGAs treated at our institution from 2010 to 2021. Demographics, treatment information, and complications were collected from the medical record. Tumor volumes were calculated from imaging obtained at initiation of treatment and at most recent follow-up. Kruskal-Wallis nonparametric testing was used to assess differences in tumor volume and follow-up duration between groups.

Results: Four patients underwent LITT (3 with LITT only), three underwent open surgical resection, and four were treated with mTOR inhibitors only. Mean percent tumor volume reduction for each group was 48.6 ± 13.8, 90.7 ± 39.8, and 67.1 ± 17.2%, respectively. No statistically significant difference was identified comparing percent tumor volume reduction between the three groups (p = 0.0513). Additionally, there was no statistically significant difference in follow-up duration between groups (p = 0.223). Only 1 patient in our series required permanent CSF diversion and 4 discontinued or decreased the dose of mTOR inhibitor due to either cost or side effects.

Conclusions: Our study suggests that LITT could be considered as a treatment option for SEGAs as it was effective in reducing tumor volume with very few complications. This modality is less invasive than open resection and may be an alternative for patients who are not candidates for mTOR inhibitors. We recommend an updated paradigm for SEGA treatment which includes LITT in select cases after consideration of patient-specific factors.

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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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