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贝伐单抗对2型神经纤维瘤病患者前庭神经鞘瘤体积的长期影响。

Long-Term Effects of Bevacizumab on Vestibular Schwannoma Volume in Neurofibromatosis Type 2 Patients.

作者信息

Killeen Daniel E, Klesse Laura, Tolisano Anthony M, Hunter Jacob B, Kutz Joe Walter

机构信息

Department of Otolaryngology - Head and Neck Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, United States.

Department of Pediatrics and Neurosurgery, University of Texas Southwestern Medical Center, Dallas, Texas, United States.

出版信息

J Neurol Surg B Skull Base. 2019 Oct;80(5):540-546. doi: 10.1055/s-0038-1676628. Epub 2018 Dec 17.

Abstract

Bevacizumab offers a medical treatment that may slow the growth of vestibular schwannomas (VS) and possibly preserve hearing in patients with neurofibromatosis type 2 (NF2). This study aims to investigate the effect of long-term bevacizumab treatment on VS progression.  Demographic, clinical, audiometric, and radiographic data were collected from the medical records of NF2 patients treated with bevacizumab at a tertiary medical center.  Eleven tumors from seven NF2 patients treated with bevacizumab were analyzed. The median age was 17 years (range: 12-47 years). Median bevacizumab treatment time was 33 months (range: 12-74 months). Of five patients with serviceable hearing pretreatment, one (20%) maintained serviceable hearing during bevacizumab therapy. Significantly slower growth rates for both tumor diameters and tumor volumes were identified during active bevacizumab treatment. Median tumor diameters and volumes during active bevacizumab treatment were 0 cm/year (range: -0.13-0.17 cm/year) and 0.1 cm /year (range: -0.92-0.41), compared with 0.37 cm/year (range: 0-1.5 cm/year,  = 0.0011) and 1.38 cm /year (range: 0.013-3.74), respectively, without bevacizumab treatment (  = 0.0263). Reduced tumor progression was noted with bevacizumab treatment utilizing both linear greatest diameter (hazard ratio 0.16,  = 0.006) and segmentation volumes (hazard ratio 0.15,  = 0.023). Complications of bevacizumab treatment included fatigue (43%), nausea/vomiting (43%), hypertension (43%), epistaxis (29%), and proteinuria (29%). One subject had a cerebrovascular accident detected on screening magnetic resonance imaging without symptoms or neurological sequelae.  Bevacizumab may reduce tumor growth rate and the risk of progression based on both volumetric and linear measurements.

摘要

贝伐单抗提供了一种医学治疗方法,它可能会减缓前庭神经鞘瘤(VS)的生长,并有可能保留2型神经纤维瘤病(NF2)患者的听力。本研究旨在调查长期使用贝伐单抗治疗对VS进展的影响。从一家三级医疗中心接受贝伐单抗治疗的NF2患者的病历中收集人口统计学、临床、听力测定和影像学数据。对7例接受贝伐单抗治疗的NF2患者的11个肿瘤进行了分析。中位年龄为17岁(范围:12 - 47岁)。贝伐单抗的中位治疗时间为33个月(范围:12 - 74个月)。在5例治疗前听力尚可的患者中,1例(20%)在贝伐单抗治疗期间维持了尚可的听力。在积极使用贝伐单抗治疗期间,肿瘤直径和肿瘤体积的生长速度均显著减慢。与未使用贝伐单抗治疗时分别为0.37 cm/年(范围:0 - 1.5 cm/年,P = 0.0011)和1.38 cm³/年(范围:0.013 - 3.74)相比,积极使用贝伐单抗治疗期间肿瘤直径和体积的中位生长速度分别为0 cm/年(范围:-0.13 - 0.17 cm/年)和0.1 cm³/年(范围:-0.92 - 0.41)(P = 0.0263)。使用线性最大直径(风险比0.16,P = 0.006)和分割体积(风险比0.15,P = 0.023)均显示贝伐单抗治疗可降低肿瘤进展。贝伐单抗治疗的并发症包括疲劳(43%)、恶心/呕吐(43%)、高血压(43%)、鼻出血(29%)和蛋白尿(29%)。1名受试者在筛查磁共振成像时被检测出脑血管意外,但无症状或神经后遗症。贝伐单抗基于体积和线性测量可能会降低肿瘤生长速度和进展风险。

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