Suppr超能文献

与李-佛美尼综合征相关的高级别胶质瘤的系统评价。

A systematic review of high-grade glioma associated with Li-Fraumeni syndrome.

作者信息

Kite Trent, Yadlapalli Vineetha, Verma Rhea, Porwal Mokshal, Herbst John, Karlovits Stephen, Wegner Rodney E, Shepard Matthew J

机构信息

Department of Neurosurgery, Allegheny Health Network Neuroscience Institute, Pittsburgh, PA, US.

Drexel University School of Medicine, Philidelphia, PA, US.

出版信息

Neurosurg Rev. 2025 Mar 10;48(1):290. doi: 10.1007/s10143-025-03437-w.

Abstract

Li-Fraumeni Syndrome (LFS) is a rare hereditary cancer syndrome characterized by an increased risk of early-onset and multiple tumors across various organ systems, predominantly linked to germline TP53 mutations. While commonly associated neoplasms include sarcomas, breast cancer, and adrenocortical carcinoma, the occurrence of high-grade gliomas (HGG), including glioblastoma multiforme (GBM), in LFS patients is less documented and typically presents at a younger age relative to sporadic cases. A systematic review following PRISMA guidelines was conducted, focusing on clinical studies and case reports that explore the association between HGG and LFS. A comprehensive PubMed search was used to capture relevant studies. The inclusion criteria focused on patients with a confirmed diagnosis of LFS and histopathologically verified HGG. A total of 248 articles were initially identified, with 8 studies meeting the final inclusion criteria after independent review and consensus. Overall, 8 studied reported on patients with either WHO grade 3 or 4 gliomas in the setting of LFS. In total these studies represent 12 patients, with 8 (66%) WHO grade 4, and 4 (33%) WHO grade 3. 9 (75%) patients underwent maximal safe resection, 5 (42%) underwent concurrent TMZ and EBRT. 9 (75%) patients underwent external beam radiation therapy (EBRT), 1 (8%) underwent intensity modulated radiation therapy (IMRT), and 1 (8%) underwent adjuvant treatment with tumor treating fields (TTF) therapy. Overall chemotherapy utilization was 75% with 9 patients receiving some form of chemotherapy. The median time to recurrence following initial treatment was 7 months (IQR: 2.00-7.00). Time to progression was variable, ranging from 5.1 months to 7 years. 64% of patients succumbed to their disease with a median OS of 17 months across studies. LFS associated HGGs are a genetically heterogenous entity. Detailed study of outcomes reported in the literature with respect to these genetics will develop further insight into therapeutic response and prognostication.

摘要

李-弗劳梅尼综合征(LFS)是一种罕见的遗传性癌症综合征,其特征是各器官系统早发和多发性肿瘤的风险增加,主要与种系TP53突变有关。虽然常见的相关肿瘤包括肉瘤、乳腺癌和肾上腺皮质癌,但LFS患者中高级别胶质瘤(HGG)的发生情况,包括多形性胶质母细胞瘤(GBM),记录较少,且相对于散发病例,发病年龄通常较小。按照PRISMA指南进行了一项系统评价,重点关注探索HGG与LFS之间关联的临床研究和病例报告。使用全面的PubMed搜索来获取相关研究。纳入标准侧重于确诊为LFS且经组织病理学证实为HGG的患者。最初共识别出248篇文章,经过独立评审和共识后,有8项研究符合最终纳入标准。总体而言,8项研究报告了LFS背景下WHO 3级或4级胶质瘤患者的情况。这些研究总共涉及12例患者,其中8例(66%)为WHO 4级,4例(33%)为WHO 3级。9例(75%)患者接受了最大安全切除,5例(42%)接受了同步替莫唑胺(TMZ)和外照射放疗(EBRT)。9例(75%)患者接受了外照射放疗(EBRT),1例(8%)接受了调强放射治疗(IMRT),1例(8%)接受了肿瘤治疗电场(TTF)治疗的辅助治疗。总体化疗使用率为75%,9例患者接受了某种形式的化疗。初始治疗后复发的中位时间为7个月(四分位间距:2.00 - 7.00)。进展时间各不相同,从5.1个月到7年不等。研究中64%的患者死于疾病,中位总生存期为17个月。与LFS相关的HGG是一种基因异质性实体。对文献中报道的这些基因相关结局进行详细研究,将进一步深入了解治疗反应和预后。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验