首页> 外文期刊>Neurosurgery >Stereotactic radiosurgery for vestibular schwannomas in patients with neurofibromatosis type 2: an analysis of tumor control, complications, and hearing preservation rates.
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Stereotactic radiosurgery for vestibular schwannomas in patients with neurofibromatosis type 2: an analysis of tumor control, complications, and hearing preservation rates.

机译:立体定向放射外科手术治疗2型神经纤维瘤病患者的前庭神经鞘瘤的肿瘤控制,并发症和听力保护率分析。

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OBJECTIVE: Vestibular schwannomas present significant management challenges in patients with neurofibromatosis Type 2 (NF2). We evaluated the results of gamma knife radiosurgery for the management of these tumors, focusing on tumor response, hearing preservation, and other factors affecting outcomes. METHODS: Stereotactic radiosurgery was performed to manage 74 schwannomas in 62 patients. Ipsilateral serviceable hearing was present in 35% of tumors before the procedure. The mean tumor volume was 5.7 cm3. The mean margin and maximum dose used were 14 and 27.5 Gy, respectively. Cox regression analyses were performed to identify factors affecting outcomes. RESULTS: The median follow-up period was 53 months, and two patients were lost to follow-up. Actuarial local control rates at were 85, 81, and 81% at 5, 10, and 15 years, respectively. Tumor volume was significant as a predictor of local control. Since 1992, using current radiosurgery techniques (magnetic resonance imaging scan targeting and reduced margin dose to 14 Gy or less), the actuarial serviceable hearing preservation rate is 73% at 1 year, 59% at 2 years, and 48% at 5 years after radiosurgery. Facial neuropathy occurred in 8% of tumors, trigeminal neuropathy occurred in 4%, and vestibular dysfunction occurred in 4%. Radiation dose and tumor volume were predictive of development of new deficits. No radiosurgery-associated secondary tumors or atypical or malignant changes were noted. CONCLUSION: Stereotactic radiosurgery is a safe and effective management modality for neurofibromatosis Type 2 vestibular schwannomas. Although results do not seem to be as good as for patients with sporadic unilateral tumors, gamma knife radiosurgery results seem favorable and indicate that radiosurgery should be strongly considered for primary tumor management in selected patients.
机译:目的:前庭神经鞘瘤对2型神经纤维瘤病(NF2)患者提出了重大的管理挑战。我们评估了伽玛刀放射外科治疗这些肿瘤的结果,重点是肿瘤反应,听力保护和其他影响预后的因素。方法:采用立体定向放射外科治疗62例患者的74例神经鞘瘤。术前35%的肿瘤存在同侧可服务的听力。平均肿瘤体积为5.7 cm3。使用的平均余量和最大剂量分别为14和27.5 Gy。进行Cox回归分析以识别影响结果的因素。结果:中位随访期为53个月,有2例患者失访。 5年,10年和15年的精算局部控制率分别为85%,81%和81%。肿瘤体积可作为局部控制的预测指标。自1992年以来,使用当前的放射外科技术(磁共振成像扫描定位和减少边缘剂量至14 Gy或更少),精算可使用的听力保存率在1年时为73%,在2年时为59%,在5年后为48%放射外科。面部神经病变发生在8%中,三叉神经病变发生在4%中,前庭功能障碍发生在4%中。辐射剂量和肿瘤体积预示着新的缺陷的发展。没有发现与放射手术有关的继发性肿瘤或非典型或恶性变化。结论:立体定向放射外科手术是治疗2型神经纤维瘤前庭神经鞘瘤的一种安全有效的治疗方法。尽管结果似乎不如散发性单侧肿瘤患者好,但伽马刀放射外科手术的结果似乎是令人满意的,表明在选定的患者中,应大力考虑放射外科治疗原发性肿瘤。

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