Department of Neurosurgery, Copenhagen, Copenhagen University Hospital, Denmark
Danish Cancer Society Research Center, Statistics and Pharmacoepidemiology, Copenhagen, Denmark.
J Neurol Neurosurg Psychiatry. 2020 Apr;91(4):378-387. doi: 10.1136/jnnp-2019-322257. Epub 2020 Feb 10.
BACKGROUND: gene alterations (-alt) have been linked to increased risk of recurrence in meningiomas, whereas the association to mortality largely remain incompletely investigated. As incongruence between clinical course and WHO grade exists, reliable biomarkers have been sought. METHODS: We applied the Preferred Reporting Items for Systematic Review and Meta-Analyses of individual participant data Statement. We compiled data from eight studies and allocated patients to -alt (n=59) or promoter wild-type (p-wt; n=618). We compared the two groups stratified for WHO grades as: incidence rates, survival probabilities and cumulative recurrences. We estimated the effects of WHO grade, age at diagnosis and sex as HRs. RESULTS: -alt occurred in 4.7%, 7.9% and 15.4% of WHO-I/WHO-II/WHO-III meningiomas, respectively. The median recurrence-free survival was 14 months for all alt patients versus 101 months for all p-wt patients. The HR for -alt was 3.74 in reference to p-wt. For all -alt patients versus all p-wt patients, the median overall survival was 58 months and 160 months, respectively. The HR for -alt was 2.77 compared with p-wt. -alt affected prognosis independent of WHO grades. Particularly, the recurrence rate was 4.8 times higher in WHO-I/-II -alt patients compared with WHO-III p-wt patients. The mortality rate was 2.7 times higher in the WHO-I and WHO-II -alt patients compared with WHO-III p-wt patients. CONCLUSIONS: -alt is an important biomarker for significantly higher risk of recurrence and death in meningiomas. -alt should be managed and surveilled aggressively. We propose that -alt analysis should be implemented as a routine diagnostic test in meningioma and integrated into the WHO classification. TRIAL REGISTRATION NUMBER: PROSPERO: CRD42018110566.
背景:基因改变(-alt)与脑膜瘤复发风险增加有关,而与死亡率的关联在很大程度上仍未得到充分研究。由于临床病程与世界卫生组织(WHO)分级之间存在不一致,因此一直在寻找可靠的生物标志物。
方法:我们应用了个体参与者数据系统评价和荟萃分析的首选报告项目声明。我们从八项研究中汇编数据,并将患者分配到-alt(n=59)或启动子野生型(p-wt;n=618)。我们按 WHO 分级对两组进行分层比较:发病率、生存率和累积复发率。我们将 WHO 分级、诊断时年龄和性别估计为 HRs。
结果:-alt 在 WHO-I/WHO-II/WHO-III 脑膜瘤中的发生率分别为 4.7%、7.9%和 15.4%。所有 alt 患者的中位无复发生存期为 14 个月,而所有 p-wt 患者为 101 个月。与 p-wt 相比,-alt 的 HR 为 3.74。对于所有的 alt 患者与所有的 p-wt 患者,中位总生存期分别为 58 个月和 160 个月。与 p-wt 相比,-alt 的 HR 为 2.77。-alt 独立于 WHO 分级影响预后。特别是,与 WHO-III p-wt 患者相比,WHO-I/WHO-II alt 患者的复发率高 4.8 倍。与 WHO-III p-wt 患者相比,WHO-I 和 WHO-II alt 患者的死亡率高 2.7 倍。
结论:-alt 是脑膜瘤复发和死亡风险显著增加的重要生物标志物。-alt 应积极管理和监测。我们建议 -alt 分析应作为脑膜瘤的常规诊断测试实施,并纳入 WHO 分类。
试验注册编号:PROSPERO:CRD42018110566。
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