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特应性病史可改善 IDH 突变型和野生型低级别胶质瘤的预后。

History of atopy confers improved outcomes in IDH mutant and wildtype lower grade gliomas.

机构信息

University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

Department of Neurosurgery, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

出版信息

J Neurooncol. 2021 Nov;155(2):133-141. doi: 10.1007/s11060-021-03854-z. Epub 2021 Oct 29.

Abstract

PURPOSE

A history of atopy or allergy has been shown to be protective against the development of glioma, however the effect of atopy on patient outcomes, especially in conjunction with the survival benefit associated with IDH mutation, has not yet been investigated, and is the focus of the study we present here.

METHODS

Low grade glioma (LGG) data from the TCGA was downloaded, along with IDH, TERT, 1p/19q and ATRX mutational status and genetic alterations. History of asthma, eczema, hay fever, animal, or food allergies, as documented in TCGA, was used to determine patient atopy status. Patients with missing variables were excluded from the study.

RESULTS

374 LGG studies were included. Patients with a history of atopy demonstrated longer overall survival (OS) compared to those without (145.3 vs. 81.5 months, p = 00.0195). IDH mutant patients with atopy had longer OS compared those without atopy (158.8 vs. 85 months, p = 0.035). Multivariate cox regression analysis demonstrated that the effects of atopy on survival were independent of IDH and histological grade, (p = 0.002, HR 0.257, 95% 0.109-0.604), (p =  < 0.001, HR 0.217, 95% 0.107-0.444), and (p = 0.004, HR 2.72, 95% 1.373-5.397), respectively. In terms of treatment outcomes, patients with atopy did not differ in treatment response compared to their counterpart. Pathway analysis demonstrated an upstream activation of the BDNF pathway (p = 0.00027).

CONCLUSION

A history of atopy confers a survival benefit in patients with diffuse low-grade glioma. Activation of the BDNF pathway may drive the observed differences.

摘要

目的

有过敏症或过敏史已被证明可预防神经胶质瘤的发生,然而,过敏症对患者预后的影响,特别是与 IDH 突变相关的生存获益,尚未得到研究,这也是我们在此提出的研究重点。

方法

从 TCGA 下载低级别胶质瘤 (LGG) 数据,以及 IDH、TERT、1p/19q 和 ATRX 突变状态和遗传改变。TCGA 中记录的哮喘、湿疹、花粉热、动物或食物过敏史用于确定患者的过敏状态。有缺失变量的患者被排除在研究之外。

结果

共纳入 374 项 LGG 研究。有过敏史的患者总生存期 (OS) 明显长于无过敏史的患者 (145.3 与 81.5 个月,p=0.0195)。有过敏史的 IDH 突变患者 OS 明显长于无过敏史的患者 (158.8 与 85 个月,p=0.035)。多变量 COX 回归分析表明,过敏对生存的影响独立于 IDH 和组织学分级,(p=0.002,HR 0.257,95% 0.109-0.604),(p<0.001,HR 0.217,95% 0.107-0.444),和 (p=0.004,HR 2.72,95% 1.373-5.397)。在治疗结果方面,过敏患者与对照组相比,治疗反应无差异。通路分析显示 BDNF 通路的上游激活 (p=0.00027)。

结论

过敏史可使弥漫性低级别神经胶质瘤患者获益。BDNF 通路的激活可能是导致观察到差异的原因。

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