• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

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

间变性少突胶质细胞瘤短期存活者的特征:POLA 网络研究。

Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study.

机构信息

Department of Neuro-Oncology, East Group Hospital, Hospices Civils de Lyon, Lyon, France.

Department of Clinical Investigation Centre (CIC-1431), Inserm, University Hospital, Besançon, France.

出版信息

Oncologist. 2022 May 6;27(5):414-423. doi: 10.1093/oncolo/oyac023.

DOI:10.1093/oncolo/oyac023
PMID:35522558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9074983/
Abstract

BACKGROUND

Anaplastic oligodendrogliomas IDH-mutant and 1p/19q codeleted (AO) occasionally have a poor outcome. Herein we aimed at analyzing their characteristics.

METHODS

We retrospectively analyzed the characteristics of 44 AO patients with a cancer-specific survival <5 years (short-term survivors, STS) and compared them with those of 146 AO patients with a survival ≥5 years (classical survivors, CS) included in the POLA network.

RESULTS

Compared to CS, STS were older (P = .0001), less frequently presented with isolated seizures (P < .0001), more frequently presented with cognitive dysfunction (P < .0001), had larger tumors (P = .= .003), a higher proliferative index (P = .= .0003), and a higher number of chromosomal arm abnormalities (P = .= .02). Regarding treatment, STS less frequently underwent a surgical resection than CS (P = .= .0001) and were more frequently treated with chemotherapy alone (P = .= .009) or with radiotherapy plus temozolomide (P = .= .05). Characteristics independently associated with STS in multivariate analysis were cognitive dysfunction, a number of mitosis > 8, and the absence of tumor resection. Based on cognitive dysfunction, type of surgery, and number of mitosis, patients could be classified into groups of standard (18%) and high (62%) risk of <5 year survival.

CONCLUSION

The present study suggests that although STS poor outcome appears to largely result from a more advanced disease at diagnosis, surgical resection may be particularly important in this population.

摘要

背景

伴 IDH 突变和 1p/19q 共缺失的间变性少突胶质细胞瘤(AO)偶有预后不良者。在此,我们旨在分析其特征。

方法

我们回顾性分析了 44 例癌症特异性生存时间<5 年(短期幸存者,STS)的 AO 患者的特征,并与纳入 POLA 网络的 146 例生存时间≥5 年(经典幸存者,CS)的 AO 患者进行了比较。

结果

与 CS 相比,STS 患者年龄更大(P=.0001),更少见单纯性癫痫发作(P<.0001),更常出现认知功能障碍(P<.0001),肿瘤更大(P=.003),增殖指数更高(P=.0003),染色体臂异常数目更多(P=.02)。在治疗方面,STS 患者较 CS 更少见行手术切除(P=.0001),更常单独接受化疗(P=.009)或接受放化疗(P=.05)。多变量分析显示,与 STS 相关的独立特征为认知功能障碍、有丝分裂数>8 个以及肿瘤未切除。基于认知功能障碍、手术类型和有丝分裂数,患者可被分为标准(18%)和高(62%)风险组,其 5 年生存率<5 年的风险较高。

结论

本研究表明,尽管 STS 预后不良似乎主要是由于诊断时疾病更晚期所致,但手术切除在该人群中可能尤为重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c8/9074983/f55fe2821367/oyac023f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c8/9074983/72f3101d9729/oyac023f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c8/9074983/f55fe2821367/oyac023f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c8/9074983/72f3101d9729/oyac023f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45c8/9074983/f55fe2821367/oyac023f0002.jpg

相似文献

1
Characteristics of Anaplastic Oligodendrogliomas Short-Term Survivors: A POLA Network Study.间变性少突胶质细胞瘤短期存活者的特征:POLA 网络研究。
Oncologist. 2022 May 6;27(5):414-423. doi: 10.1093/oncolo/oyac023.
2
Ki-67 and MCM6 labeling indices are correlated with overall survival in anaplastic oligodendroglioma, IDH1-mutant and 1p/19q-codeleted: a multicenter study from the French POLA network.Ki-67 和 MCM6 标记指数与 IDH1 突变和 1p/19q 共缺失的间变性少突胶质细胞瘤的总生存相关:来自法国 POLA 网络的多中心研究。
Brain Pathol. 2020 May;30(3):465-478. doi: 10.1111/bpa.12788. Epub 2019 Oct 10.
3
Genetic landscape of extreme responders with anaplastic oligodendroglioma.间变性少突胶质细胞瘤极端反应者的基因图谱
Oncotarget. 2017 May 30;8(22):35523-35531. doi: 10.18632/oncotarget.16773.
4
Efficacy of initial temozolomide for high-risk low grade gliomas in a phase II AINO (Italian Association for Neuro-Oncology) study: a post-hoc analysis within molecular subgroups of WHO 2016.意大利神经肿瘤学会(Italian Association for Neuro-Oncology)一项 II 期研究中初始替莫唑胺治疗高危低级别胶质瘤的疗效:根据 2016 年 WHO 分子亚组的事后分析。
J Neurooncol. 2019 Oct;145(1):115-123. doi: 10.1007/s11060-019-03277-x. Epub 2019 Sep 25.
5
Multicenter phase II study of temozolomide and myeloablative chemotherapy with autologous stem cell transplant for newly diagnosed anaplastic oligodendroglioma.多中心二期研究:替莫唑胺联合大剂量化疗联合自体造血干细胞移植治疗新诊断的间变性少突胶质细胞瘤。
Neuro Oncol. 2017 Oct 1;19(10):1380-1390. doi: 10.1093/neuonc/nox086.
6
Impact of 1p/19q codeletion and histology on outcomes of anaplastic gliomas treated with radiation therapy and temozolomide.1p/19q 联合缺失与组织学特征对放化疗治疗间变性神经胶质瘤患者预后的影响。
Int J Radiat Oncol Biol Phys. 2015 Feb 1;91(2):268-76. doi: 10.1016/j.ijrobp.2014.10.027.
7
Gliosarcoma arising from oligodendroglioma, IDH mutant and 1p/19q codeleted.起源于少突胶质细胞瘤的胶质肉瘤,异柠檬酸脱氢酶(IDH)突变且1p/19q共缺失。
Neuropathology. 2018 Feb;38(1):41-46. doi: 10.1111/neup.12406. Epub 2017 Aug 15.
8
Allelic loss of chromosome 1p and radiotherapy plus chemotherapy in patients with oligodendrogliomas.少突胶质细胞瘤患者1号染色体短臂等位基因缺失与放疗加化疗
Int J Radiat Oncol Biol Phys. 2000 Oct 1;48(3):825-30. doi: 10.1016/s0360-3016(00)00703-3.
9
The Correlation Between 1p/19q Codeletion, IDH1 Mutation, p53 Overexpression and Their Prognostic Roles in 41 Turkish Anaplastic Oligodendroglioma Patients.41例土耳其间变性少突胶质细胞瘤患者中1p/19q共缺失、IDH1突变、p53过表达之间的相关性及其预后作用
Turk Neurosurg. 2017;27(5):682-689. doi: 10.5137/1019-5149.JTN.16832-15.1.
10
Favorable long-term outcome of low-grade oligodendrogliomas irrespective of 1p/19q status when treated without radiotherapy.低级别少突胶质细胞瘤患者无论 1p/19q 状态如何,如果不接受放疗,均可获得良好的长期预后。
J Neurooncol. 2011 May;102(3):443-9. doi: 10.1007/s11060-010-0340-4. Epub 2010 Aug 19.

引用本文的文献

1
Hemizygous deletion of cyclin-dependent kinase inhibitor 2A/B with p16 immuno-negative and methylthioadenosine phosphorylase retention predicts poor prognosis in IDH-mutant adult glioma.细胞周期蛋白依赖性激酶抑制剂2A/B的半合子缺失伴p16免疫阴性和甲硫腺苷磷酸化酶保留预示着异柠檬酸脱氢酶(IDH)突变型成人胶质瘤的预后不良。
Neurooncol Adv. 2024 May 8;6(1):vdae069. doi: 10.1093/noajnl/vdae069. eCollection 2024 Jan-Dec.
2
The biological significance of tumor grade, age, enhancement, and extent of resection in IDH-mutant gliomas: How should they inform treatment decisions in the era of IDH inhibitors?IDH 突变型胶质瘤中肿瘤分级、年龄、强化和切除程度的生物学意义:在 IDH 抑制剂时代,它们应如何影响治疗决策?
Neuro Oncol. 2024 Oct 3;26(10):1805-1822. doi: 10.1093/neuonc/noae107.
3

本文引用的文献

1
Survival outcome and prognostic factors in anaplastic oligodendroglioma: a single-institution study of 95 cases.间变性少突胶质细胞瘤的生存结果和预后因素:单机构 95 例研究。
Sci Rep. 2020 Nov 19;10(1):20162. doi: 10.1038/s41598-020-77228-2.
2
CODEL: phase III study of RT, RT + TMZ, or TMZ for newly diagnosed 1p/19q codeleted oligodendroglioma. Analysis from the initial study design.CODEL:新诊断的 1p/19q 共缺失型少突胶质细胞瘤接受放疗、放疗 +TMZ 或 TMZ 治疗的 III 期研究。基于初始研究设计的分析。
Neuro Oncol. 2021 Mar 25;23(3):457-467. doi: 10.1093/neuonc/noaa168.
3
Erratum. Extent of resection, molecular signature, and survival in 1p19q-codeleted gliomas.
Long-term follow up of patients with WHO grade 2 oligodendroglioma.WHO 分级 2 级少突胶质细胞瘤患者的长期随访。
J Neurooncol. 2023 Aug;164(1):65-74. doi: 10.1007/s11060-023-04368-6. Epub 2023 Aug 21.
4
A Multigene Signature Associated with Progression-Free Survival after Treatment for IDH Mutant and 1p/19q Codeleted Oligodendrogliomas.一种与异柠檬酸脱氢酶(IDH)突变型和1p/19q共缺失型少突胶质细胞瘤治疗后无进展生存期相关的多基因特征。
Cancers (Basel). 2023 Jun 6;15(12):3067. doi: 10.3390/cancers15123067.
5
An expanded role for surgery in grade 3 1p/19q co-deleted oligodendroglioma.手术在1p/19q共缺失三级少突胶质细胞瘤中的作用扩大。
Neurooncol Adv. 2023 Apr 21;5(1):vdad046. doi: 10.1093/noajnl/vdad046. eCollection 2023 Jan-Dec.
J Neurosurg. 2020 Jun 5;134(5):1675. doi: 10.3171/2020.5.JNS192767a. Print 2021 May 1.
4
Imaging growth as a predictor of grade of malignancy and aggressiveness of IDH-mutant and 1p/19q-codeleted oligodendrogliomas in adults.将影像学表现作为成人 IDH 突变型和 1p/19q 联合缺失型少突胶质细胞瘤恶性程度和侵袭性分级的预测指标。
Neuro Oncol. 2020 Jul 7;22(7):993-1005. doi: 10.1093/neuonc/noaa022.
5
CDKN2A homozygous deletion is a strong adverse prognosis factor in diffuse malignant IDH-mutant gliomas.CDKN2A 纯合缺失是弥漫性恶性 IDH 突变型神经胶质瘤的一个强烈不良预后因素。
Neuro Oncol. 2019 Dec 17;21(12):1519-1528. doi: 10.1093/neuonc/noz124.
6
A multi-institutional analysis of clinical outcomes and patterns of care of 1p/19q codeleted oligodendrogliomas treated with adjuvant or salvage radiation therapy.多机构分析 1p/19q 共缺失少突胶质细胞瘤辅助或挽救性放疗的临床结果和治疗模式。
J Neurooncol. 2020 Jan;146(1):121-130. doi: 10.1007/s11060-019-03344-3. Epub 2019 Nov 18.
7
Ki-67 and MCM6 labeling indices are correlated with overall survival in anaplastic oligodendroglioma, IDH1-mutant and 1p/19q-codeleted: a multicenter study from the French POLA network.Ki-67 和 MCM6 标记指数与 IDH1 突变和 1p/19q 共缺失的间变性少突胶质细胞瘤的总生存相关:来自法国 POLA 网络的多中心研究。
Brain Pathol. 2020 May;30(3):465-478. doi: 10.1111/bpa.12788. Epub 2019 Oct 10.
8
Extent of resection and survival for oligodendroglioma: a U.S. population-based study.少突胶质细胞瘤的切除范围与生存:一项基于美国人群的研究。
J Neurooncol. 2019 Sep;144(3):591-601. doi: 10.1007/s11060-019-03261-5. Epub 2019 Aug 12.
9
Polysomy is associated with poor outcome in 1p/19q codeleted oligodendroglial tumors.多倍体与 1p/19q 联合缺失型少突胶质细胞瘤的不良预后相关。
Neuro Oncol. 2019 Sep 6;21(9):1164-1174. doi: 10.1093/neuonc/noz098.
10
Prognostic factors associated with survival in patients with anaplastic oligodendroglioma.与间变性少突胶质细胞瘤患者生存相关的预后因素。
PLoS One. 2019 Jan 30;14(1):e0211513. doi: 10.1371/journal.pone.0211513. eCollection 2019.