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原发性多形性胶质母细胞瘤的长期生存:一项针对保加利亚患者的临床研究。

Long-term survival with primary glioblastoma multiforme: a clinical study in bulgarian patients.

作者信息

Naydenov E, Tzekov C, Minkin K, Nachev S, Romansky K, Bussarsky V

机构信息

Department of Neurosurgery, University Hospital 'St. Ivan Rilski', Sofia, Bulgaria.

出版信息

Case Rep Oncol. 2011 Jan 4;4(1):1-11. doi: 10.1159/000323432.

DOI:10.1159/000323432
PMID:21537375
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3085065/
Abstract

Glioblastoma multiforme (GBM) is the most common and aggressive primary brain tumor with an extremely poor prognosis in spite of multimodal treatment approaches. The estimated median survival in cases with GBM is about 12-16 months. Those patients who survive =3 years after the initial diagnosis are defined as long-term survivors. In this study, we retrospectively analyze 50 consecutive cases of Bulgarian patients with newly diagnosed GBM surgically treated at our institution for a period of 1 year. Four of them survived for more than 36 months after the initial intervention. The histological re-examination revealed features typical of primary GBM in 3 of these cases, which are described in detail in the present paper. A brief review of the relevant literature is also given.

摘要

多形性胶质母细胞瘤(GBM)是最常见且侵袭性最强的原发性脑肿瘤,尽管采用了多模式治疗方法,其预后仍极差。GBM患者的估计中位生存期约为12 - 16个月。那些在初次诊断后存活≥3年的患者被定义为长期幸存者。在本研究中,我们回顾性分析了我院1年内手术治疗的50例新诊断为GBM的保加利亚连续病例。其中4例在初次干预后存活超过36个月。组织学重新检查显示,这些病例中有3例具有原发性GBM的典型特征,本文将对其进行详细描述。此外,还对相关文献进行了简要综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/00614742df6e/cro0004-0001-f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/0d1e6929d99a/cro0004-0001-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/37d97fee6df8/cro0004-0001-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/0e15aaf150a1/cro0004-0001-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/b01627c79f0c/cro0004-0001-f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/42604e1dddf8/cro0004-0001-f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/00614742df6e/cro0004-0001-f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/0d1e6929d99a/cro0004-0001-f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/37d97fee6df8/cro0004-0001-f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/0e15aaf150a1/cro0004-0001-f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/b01627c79f0c/cro0004-0001-f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/42604e1dddf8/cro0004-0001-f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07e/3085065/00614742df6e/cro0004-0001-f06.jpg

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本文引用的文献

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Case Rep Oncol. 2009 Jul 17;2(2):103-110. doi: 10.1159/000228545.
2
The transcriptional network for mesenchymal transformation of brain tumours.脑肿瘤间质转化的转录网络。
Nature. 2010 Jan 21;463(7279):318-25. doi: 10.1038/nature08712. Epub 2009 Dec 23.
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A proposed classification system that projects outcomes based on preoperative variables for adult patients with glioblastoma multiforme.
Cells. 2020 Aug 8;9(8):1859. doi: 10.3390/cells9081859.
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Cycling Quiescence in Temozolomide Resistant Glioblastoma Cells Is Partly Explained by microRNA-93 and -193-Mediated Decrease of Cyclin D.替莫唑胺耐药的胶质母细胞瘤细胞中的细胞周期静止部分是由微小RNA-93和-193介导的细胞周期蛋白D减少所解释的。
Front Pharmacol. 2019 Feb 22;10:134. doi: 10.3389/fphar.2019.00134. eCollection 2019.
5
Serum immunoreactivity of cancer/testis antigen OY-TES-1 and its tissues expression in glioma.癌/睾丸抗原OY-TES-1的血清免疫反应性及其在胶质瘤中的组织表达。
Oncol Lett. 2017 May;13(5):3080-3086. doi: 10.3892/ol.2017.5799. Epub 2017 Mar 3.
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Temozolomide resistance and tumor recurrence: Halting the Hedgehog.替莫唑胺耐药与肿瘤复发:阻断刺猬信号通路
Cancer Cell Microenviron. 2015;2(2). doi: 10.14800/ccm.747. Epub 2015 May 7.
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Comprehensive analysis of the functional microRNA-mRNA regulatory network identifies miRNA signatures associated with glioma malignant progression.全面分析功能 miRNA-mRNA 调控网络,确定与胶质瘤恶性进展相关的 miRNA 特征。
Nucleic Acids Res. 2013 Dec;41(22):e203. doi: 10.1093/nar/gkt1054. Epub 2013 Nov 4.
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Pediatric glioblastoma: clinico-radiological profile and factors affecting the outcome.小儿胶质母细胞瘤:临床放射学特征及影响预后的因素
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Neuro Oncol. 2009 Dec;11(6):833-41. doi: 10.1215/15228517-2008-123.