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首页> 外文期刊>Journal of clinical neuroscience: official journal of the Neurosurgical Society of Australasia >Atypical and malignant meningiomas: Considerations for treatment and efficacy of radiotherapy
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Atypical and malignant meningiomas: Considerations for treatment and efficacy of radiotherapy

机译:非典型和恶性脑膜瘤:放射治疗的治疗和疗效考虑

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The purpose of this study was to add to the current body of literature which is aimed at establishing the role of postoperative adjuvant radiotherapy (RT) in the treatment of atypical and malignant meningiomas. Meningiomas are the most frequently reported primary intracranial tumours, accounting for more than 35%. The majority of meningiomas are benign, with atypical and malignant tumours accounting for only 6-18%. Utilising a prospective multi-institutional database, we retrospectively reviewed 67 patients with documented World Health Organisation (WHO) Grade II/III meningiomas, diagnosed between 1989 and 2012 and resected at two major Australian hospitals. Nine patients were excluded and the remaining 58 were analysed. The patient demographics, tumour characteristics, surgical details and adjuvant therapy were retrieved. Kaplan-Meier curves were used to compare the survival of patients treated with RT versus surgery alone. The 3 year progression free survival (PFS) and overall survival (OS) were 44 and 76% for the entire cohort, respectively. Of the patients who had gross total resections, 42% had 3 years PFS and 77% had 3 years OS, which was not significantly different from those with subtotal resection. The overall median survival was 11.0 years, 12.2 for atypical and 1.6 for malignant meningiomas. The patients with malignant meningiomas were 14 times as likely to receive RT as the patients with atypical meningiomas. The patients who received RT had a 3 year PFS of 63% compared to 40% in those who did not receive radiation. The 3 year OS was 31% higher for females than males. Histopathological progression was noted in 17% of our cohort. This study reinforces a number of important factors that should be considered when treating patients presenting with WHO Grade II and III meningiomas, including sex, Potential for grade progression, and the lack of evidence for adjuvant RT and the timing thereof. (C) 2015 Elsevier Ltd. All rights reserved.
机译:这项研究的目的是增加目前的文献,旨在确定术后辅助放疗(RT)在治疗非典型和恶性脑膜瘤中的作用。脑膜瘤是最常报告的原发性颅内肿瘤,占35%以上。大多数脑膜瘤是良性的,非典型和恶性肿瘤仅占6-18%。利用前瞻性多机构数据库,我们回顾性研究了67例世界卫生组织(WHO)II / III级脑膜瘤的患者,这些患者在1989年至2012年之间被诊断出并在澳大利亚的两家主要医院切除。 9名患者被排除在外,其余58名被分析。检索患者的人口统计资料,肿瘤特征,手术细节和辅助治疗。 Kaplan-Meier曲线用于比较接受RT治疗与单纯手术治疗的患者的生存期。整个队列的3年无进展生存期(PFS)和总生存期(OS)分别为44%和76%。在全部切除的患者中,有42%的患者接受了3年的PFS,而77%的患者接受了3年的OS,这与进行大范围切除的患者无显着差异。总体中位生存期为11.0年,非典型性为12.2岁,恶性脑膜瘤为1.6岁。恶性脑膜瘤患者接受非典型性脑膜瘤患者放疗的可能性是非典型脑膜瘤患者的14倍。接受放疗的患者3年PFS为63%,而未接受放疗的患者为40%。女性的3年OS比男性高31%。在我们的队列中有17%注意到组织病理学进展。这项研究加强了治疗具有WHO II级和III级脑膜瘤的患者时应考虑的许多重要因素,包括性别,分级进展的潜力以及缺乏辅助性RT证据和时机。 (C)2015 Elsevier Ltd.保留所有权利。

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