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三叉神经鞘瘤的立体定向放射外科治疗:肿瘤控制与功能保留 临床文章

Stereotactic radiosurgery for trigeminal schwannoma: tumor control and functional preservation Clinical article.

作者信息

Kano Hideyuki, Niranjan Ajay, Kondziolka Douglas, Flickinger John C, Dade Lunsford L

机构信息

Departments of Neurological Surgery, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA.

出版信息

J Neurosurg. 2009 Mar;110(3):553-8. doi: 10.3171/2008.7.jns0812.

Abstract

OBJECT

To evaluate outcome predictors after stereotactic radiosurgery (SRS) in patients with trigeminal schwannomas, the authors compared tumor control, functional preservation, and complications with tumor grade, tumor volume, patient age, and tumor imaging characteristics.

METHODS

The records of 33 consecutive patients with trigeminal schwannoma treated via Gamma Knife surgery were retrospectively reviewed. The median patient age was 49.5 years (range 15.1-82.5 years). Eleven patients had undergone prior tumor resection. Two patients had neurofibromatosis Type 2. Lesions were classified as root type (6 tumors), ganglion type (17 tumors), and dumbbell type (10 tumors) based on their location. The median radiosurgery target volume was 4.2 cm3 (range 0.5-18.0 cm3), and the median dose to the tumor margin was 15.0 Gy (range 12-20 Gy).

RESULTS

At an average of 6 years (range 7.2-147.9 months), the rate of progression-free survival (PFS) at 1, 5, and 10 years after SRS was 97.0, 82.0, and 82.0%, respectively. Factors associated with improved PFS included female sex, smaller tumor volume, and a root or ganglion tumor type. Neurological symptoms or signs improved in 11 (33.3%) of 33 patients and were unchanged in 19 (57.6%). Three patients (9.1%) had symptomatic disease progression. Patients who had not undergone a prior tumor resection were significantly more likely to show improvement in neurological symptoms or signs.

CONCLUSIONS

Stereotactic radiosurgery is an effective and minimally invasive management option in patients with residual or newly diagnosed trigeminal schwannomas. Predictors of a better treatment response included female sex, smaller tumor volume, root or ganglion tumor type, and the application of SRS as the primary treatment.

摘要

目的

为评估三叉神经鞘瘤患者接受立体定向放射外科治疗(SRS)后的预后预测因素,作者比较了肿瘤控制、功能保留以及并发症与肿瘤分级、肿瘤体积、患者年龄和肿瘤影像学特征之间的关系。

方法

回顾性分析33例连续接受伽玛刀手术治疗的三叉神经鞘瘤患者的病历。患者年龄中位数为49.5岁(范围15.1 - 82.5岁)。11例患者曾接受过肿瘤切除术。2例患者患有2型神经纤维瘤病。根据病变位置将其分为根型(6例肿瘤)、神经节型(17例肿瘤)和哑铃型(10例肿瘤)。立体定向放射外科治疗的中位靶体积为4.2 cm³(范围0.5 - 18.0 cm³),肿瘤边缘的中位剂量为15.0 Gy(范围12 - 20 Gy)。

结果

平均随访6年(范围7.2 - 147.9个月),SRS后1年、5年和10年的无进展生存率(PFS)分别为97.0%、82.0%和82.0%。与PFS改善相关的因素包括女性、较小的肿瘤体积以及根型或神经节型肿瘤。33例患者中有11例(33.3%)神经症状或体征改善,19例(57.6%)无变化。3例患者(9.1%)出现症状性疾病进展。未接受过先前肿瘤切除术的患者神经症状或体征改善的可能性显著更高。

结论

立体定向放射外科治疗是残留或新诊断的三叉神经鞘瘤患者的一种有效且微创的治疗选择。更好治疗反应的预测因素包括女性、较小的肿瘤体积、根型或神经节型肿瘤以及将SRS作为主要治疗方法的应用。

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