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颅底脑膜瘤伴颅外扩展的临床特征、个体化治疗及长期手术结果

Clinial Features, Individualized Treatment and Long-Term Surgical Outcomes of Skull Base Meningiomas With Extracranial Extensions.

作者信息

Liu Houjie, Qian Haipeng, Li Xueji, Zuo Fuxing, Meng Xiaoli, Liu Shaoyan, Wan Jinghai

机构信息

Department of Neurosurgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.

Department of Head and Neck Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.

出版信息

Front Oncol. 2020 Jun 30;10:1054. doi: 10.3389/fonc.2020.01054. eCollection 2020.

Abstract

Skull base meningiomas with extracranial extensions are rarely described. This study describes the clinical features, surgical management and clinical outcomes of these rare tumors and investigates risk factors associated with progression-free survival (PFS). The clinical data of 34 consecutive patients who underwent surgery for skull base meningiomas with extracranial extensions from 2007 to 2018 were retrospectively collected and analyzed. The mean patient age was 47.9 ± 13.9 years; 50.0% were male. The most common symptoms on admission were ophthalmic. All patients underwent a multidisciplinary consultation before surgery, and received individualized surgical management. The gross total resection (GTR) rate was 55.9% (19/34). Twelve patients received post-operative adjuvant radiotherapy (RT). Twelve patients experienced tumor recurrence during the follow-up period. The median PFS duration was 54 months. The mean overall survival (OS) duration was 111 months. By univariate analysis, a higher histological grade (WHO grade II and III), Ki-67 LI ≥ 5 and the extent of resection (EOR) were significantly associated with tumor recurrence. Multivariate analysis revealed Ki-67 LI ≥ 5, the EOR and adjuvant RT as prognostic factor of PFS. These relatively rare meningiomas are difficult to resect and have a poor prognosis; they are more common in males and have a higher histological grade than intracranial meningiomas. Multidisciplinary collaboration and individualized surgical strategies are crucial for surgically managing these complex tumors. Total removal of the tumor remains challenging. Subtotal resection (STR) or partial resection (PR) followed by RT is a reasonable strategy when radical resection is infeasible. Adjuvant RT should be recommended especially for tumors with histopathological risk factors (Ki-67 LI ≥ 5 or high histological grade).

摘要

颅底脑膜瘤伴颅外扩展的情况鲜有报道。本研究描述了这些罕见肿瘤的临床特征、手术治疗及临床结局,并探讨了与无进展生存期(PFS)相关的危险因素。回顾性收集并分析了2007年至2018年连续34例接受手术治疗的颅底脑膜瘤伴颅外扩展患者的临床资料。患者平均年龄为47.9±13.9岁;男性占50.0%。入院时最常见的症状为眼部症状。所有患者术前均接受了多学科会诊,并接受了个体化手术治疗。大体全切(GTR)率为55.9%(19/34)。12例患者术后接受了辅助放疗(RT)。12例患者在随访期间出现肿瘤复发。PFS的中位持续时间为54个月。总生存期(OS)的平均持续时间为111个月。单因素分析显示,较高的组织学分级(世界卫生组织II级和III级)、Ki-67标记指数(LI)≥5以及切除范围(EOR)与肿瘤复发显著相关。多因素分析显示,Ki-67 LI≥5、EOR和辅助放疗是PFS的预后因素。这些相对罕见的脑膜瘤难以切除且预后较差;它们在男性中更常见,且组织学分级高于颅内脑膜瘤。多学科协作和个体化手术策略对于手术治疗这些复杂肿瘤至关重要。肿瘤的完全切除仍然具有挑战性。当根治性切除不可行时,次全切除(STR)或部分切除(PR)后行放疗是一种合理的策略。尤其对于具有组织病理学危险因素(Ki-67 LI≥5或高组织学分级)的肿瘤,应推荐辅助放疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8063/7340145/a017631287a2/fonc-10-01054-g0001.jpg

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