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MNGI-07. THE ANAPLASTIC MENINGIOMA INTERNATIONAL CONSORTIUM (AMICo) RETROSPECTIVE STUDY OF TREATMENT AND OUTCOME OF PATIENTS WITH ANAPLASTIC MENINGIOMAS

机译:MNGI-07。再生性脑膜瘤患者的治疗和结果回顾性国际回顾性研究

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摘要

Anaplastic meningiomas are rare, comprising only 1–2% of all meningiomas, and limited data on its natural history and response to treatment. An international retrospective study using 2016 Classification of the Tumours of the CNS was used to identify grade 3 meningiomas. Anonymised clinical and radiological data were collected in a uniform manner from 21 centres.RESULTS355 patients were identified to have an anaplastic meningioma. 57% cases arose de novo and 43% were progressed from lower grade; 20% directly from grade 1, 15% from grade 1 via grade 2 and 65% from grade 2. Female predominated among de novo and males among the progressive cases, with M/F ratios 0.8 and 1.4, respectively (p=0.02). De novo tumours were, on average, larger than progressive (51cc and 27cc, respectively; p=0.002). De novo cases predominated in sphenoid wing and ventricular locations, while progressive cases predominated in anterior fossa midline locations. The median survival of patient from the first diagnosis of anaplastic meningioma (index surgery) was 99 and 30 months for de novoand progressive cases, respectively (p<0.0001). Independent factors for survival were degree of resection (p=0.23) and administration of radiotherapy (p<0.001). Among the progressive anaplastic meningiomas, the longest survival was achieved in patients who received radiotherapy both before and after the index surgery. Those receiving radiotherapy only after lived longer than those who received radiotherapy before the index surgery. Those who received no radiotherapy had shortest survival. The difference in growth between surgery only and surgery and radiotherapy groups was significant (17.6%/month versus 5.3%/month; p = 0.038). Here in we present the largest cohort of patients with anaplastic meningiomas allowing detailed analysis of natural history and response to treatment in de novo and progressive anaplastic meningiomas.
机译:间变性脑膜瘤很少见,仅占所有脑膜瘤的1-2%,而且关于其自然病史和对治疗的反应的数据有限。使用2016年《中枢神经系统肿瘤分类》进行的国际回顾性研究确定了3级脑膜瘤。从21个中心以统一的方式收集了匿名的临床和放射学数据。结果确定了355名患有间变性脑膜瘤的患者。从头开始的案件占57%,从低年级进展为43%;从1年级直接获得20%,从1年级通过2年级获得15%,从2年级获得65%,在进行性病例中,女性从头开始,男性占主导地位,男/女比分别为0.8和1.4(p = 0.02)。从头算起的新肿瘤平均大于进行性肿瘤(分别为51cc和27cc; p = 0.002)。新发病例在蝶骨翼和心室位置占优势,而进展期病例在前窝中线位置占优势。新生和进行性病例首次诊断为间变性脑膜瘤(指数手术)的患者中位生存期分别为99和30个月(p <0.0001)。生存的独立因素是切除程度(p = 0.23)和放疗的使用(p <0.001)。在进行性间变性的脑膜瘤中,在分度手术前后均接受放射治疗的患者生存期最长。仅在放疗后才接受放疗的人比在索引手术之前接受放疗的人寿命更长。那些没有接受放射治疗的人生存期最短。仅手术组与手术和放疗组之间的生长差异显着(分别为17.6%/月和5.3%/月; p = 0.038)。在这里,我们介绍了间变性脑膜瘤患者的最大队列,可以详细分析自然病史和从头治疗和进行性间变性脑膜瘤对治疗的反应。

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