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1号染色体长臂/19号染色体短臂共多倍体预示着星形细胞瘤患者更长的生存期。

1q/19p co-polysomy predicts longer survival in patients with astrocytic gliomas.

作者信息

Zeng Wei, Ren Xiaohui, Cui Yong, Jiang Haihui, Zhang Xiuru, Lin Song

机构信息

Department of Neurosurgery, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.

China National Clinical Research Center for Neurological Diseases, Beijing, China.

出版信息

Oncotarget. 2017 May 16;8(40):67104-67116. doi: 10.18632/oncotarget.17947. eCollection 2017 Sep 15.

DOI:10.18632/oncotarget.17947
PMID:28978019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5620159/
Abstract

Recently, we reported that 1q/19p co-polysomy predicted poor prognosis in oligodendroglial tumors. In this study, we aimed to retrospectively analyze the prognostic significance of 1q/19p polysomy in two large cohorts of astrocytic gliomas classified by the 2007 and 2016 WHO classification of tumors of the central nervous system. 1q/19p polysomy was detected using the FISH method, and factors that correlated with polysomy were analyzed by logistic regression. Survival analysis was used to identify independent prognostic factors correlated with survival. In the WHO astrocytic glioma cohort (N=421), co-polysomy was associated with a younger age, whereas single polysomy was associated with higher tumor grades and a higher Ki-67 index (<0.05). Co-polysomy predicted longer survival, and single polysomy predicted shorter survival (<0.05). In multivariate analysis, co-polysomy maintained an independent prognostic impact on survival (=0.001) after adjustment for age, KPS, grade, removal degree, tumor size, Ki-67 index, and IDH1/2. In the WHO cohort (N=572), we validated the prognostic merit of co-polysomy after adjusting for related factors. In conclusion, 1q/19p co-polysomy added prognostic information in cases of astrocytic glioma and could be used for molecular stratification of this disease.

摘要

最近,我们报道了1q/19p共多体性预测少突胶质细胞瘤预后不良。在本研究中,我们旨在回顾性分析1q/19p多体性在根据2007年和2016年世界卫生组织中枢神经系统肿瘤分类划分的两个大型星形细胞瘤队列中的预后意义。采用荧光原位杂交(FISH)方法检测1q/19p多体性,并通过逻辑回归分析与多体性相关的因素。生存分析用于确定与生存相关的独立预后因素。在世界卫生组织星形细胞瘤队列(N = 421)中,共多体性与较年轻的年龄相关,而单多体性与较高的肿瘤分级和较高的Ki-67指数相关(<0.05)。共多体性预测生存期较长,单多体性预测生存期较短(<0.05)。在多变量分析中,在对年龄、KPS、分级、切除程度、肿瘤大小、Ki-67指数和异柠檬酸脱氢酶1/2(IDH1/2)进行调整后,共多体性对生存仍具有独立的预后影响(=0.001)。在世界卫生组织队列(N = 572)中,我们在对相关因素进行调整后验证了共多体性的预后价值。总之,1q/19p共多体性为星形细胞瘤病例增加了预后信息,可用于该疾病的分子分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/bfe6b1369249/oncotarget-08-67104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/968f12a1f0f2/oncotarget-08-67104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/4792b2f4277d/oncotarget-08-67104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/e956dd65ccff/oncotarget-08-67104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/3da97f0b4a6e/oncotarget-08-67104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/bfe6b1369249/oncotarget-08-67104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/968f12a1f0f2/oncotarget-08-67104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/4792b2f4277d/oncotarget-08-67104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/e956dd65ccff/oncotarget-08-67104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/3da97f0b4a6e/oncotarget-08-67104-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0372/5620159/bfe6b1369249/oncotarget-08-67104-g005.jpg

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本文引用的文献

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Acta Neuropathol. 2016 Jun;131(6):803-20. doi: 10.1007/s00401-016-1545-1. Epub 2016 May 9.
2
The influence of maximum safe resection of glioblastoma on survival in 1229 patients: Can we do better than gross-total resection?1229例胶质母细胞瘤患者最大安全切除对生存的影响:我们能否比全切除做得更好?
J Neurosurg. 2016 Apr;124(4):977-88. doi: 10.3171/2015.5.JNS142087. Epub 2015 Oct 23.
3
Glioma Groups Based on 1p/19q, IDH, and TERT Promoter Mutations in Tumors.
基于肿瘤中1p/19q、异柠檬酸脱氢酶(IDH)和端粒酶逆转录酶(TERT)启动子突变的胶质瘤分组
N Engl J Med. 2015 Jun 25;372(26):2499-508. doi: 10.1056/NEJMoa1407279. Epub 2015 Jun 10.
4
Molecular profiling of long-term survivors identifies a subgroup of glioblastoma characterized by chromosome 19/20 co-gain.对长期幸存者进行分子谱分析,确定了胶质母细胞瘤的一个亚组,其特征是染色体 19/20 共同增益。
Acta Neuropathol. 2015 Sep;130(3):419-34. doi: 10.1007/s00401-015-1427-y. Epub 2015 May 1.
5
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J Neurooncol. 2014 Oct;120(1):131-8. doi: 10.1007/s11060-014-1526-y. Epub 2014 Jul 10.
6
Glioblastoma and other malignant gliomas: a clinical review.胶质母细胞瘤和其他恶性胶质瘤:临床综述。
JAMA. 2013 Nov 6;310(17):1842-50. doi: 10.1001/jama.2013.280319.
7
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8
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J Neuropathol Exp Neurol. 2012 Jul;71(7):618-24. doi: 10.1097/NEN.0b013e31825b5f7a.
9
Losing balance: the origin and impact of aneuploidy in cancer.失去平衡:癌症中非整倍体的起源和影响。
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