• 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

相似文献

1
Treatment and outcome of intracranial ependymoma after first relapse in the 2nd AIEOP protocol.2 项 AIEOP 方案中初次复发后颅内室管膜瘤的治疗和结果。
Neuro Oncol. 2022 Mar 12;24(3):467-479. doi: 10.1093/neuonc/noab230.
2
Treatment and outcome of pediatric intracranial ependymoma after first relapse.儿童颅内室管膜瘤首次复发后的治疗和转归。
J Neurooncol. 2022 May;157(3):385-396. doi: 10.1007/s11060-022-03975-z. Epub 2022 Feb 28.
3
Extent of re-excision, sequence/timing of salvage re-irradiation, and disease-free interval impact upon clinical outcomes in recurrent/progressive ependymoma.复发性/进展性室管膜瘤中再次切除范围、挽救性再放疗的顺序/时间以及无疾病间期对临床结果的影响。
J Neurooncol. 2020 Apr;147(2):405-415. doi: 10.1007/s11060-020-03434-7. Epub 2020 Feb 18.
4
Pediatric intracranial ependymoma: correlating signs and symptoms at recurrence with outcome in the second prospective AIEOP protocol follow-up.儿童颅内室管膜瘤:在第二个前瞻性 AIEOP 方案随访中,复发时的症状和体征与结局的相关性。
J Neurooncol. 2018 Nov;140(2):457-465. doi: 10.1007/s11060-018-2974-6. Epub 2018 Aug 14.
5
Outcomes after first relapse of childhood intracranial ependymoma.儿童颅内室管膜瘤首次复发后的结局
Pediatr Blood Cancer. 2021 Aug;68(8):e28930. doi: 10.1002/pbc.28930. Epub 2021 Feb 9.
6
Final results of the second prospective AIEOP protocol for pediatric intracranial ependymoma.小儿颅内室管膜瘤的第二项前瞻性AIEOP方案的最终结果。
Neuro Oncol. 2016 Oct;18(10):1451-60. doi: 10.1093/neuonc/now108. Epub 2016 May 18.
7
Relapsed intracranial ependymoma in children in the UK: patterns of relapse, survival and therapeutic outcome.英国儿童复发性颅内室管膜瘤:复发模式、生存率及治疗结果
Eur J Cancer. 2009 Jul;45(10):1815-23. doi: 10.1016/j.ejca.2009.03.018. Epub 2009 May 7.
8
Primary postoperative chemotherapy without radiotherapy for intracranial ependymoma in children: the UKCCSG/SIOP prospective study.儿童颅内室管膜瘤术后单纯化疗不联合放疗:英国儿童癌症协作组/国际小儿肿瘤学会前瞻性研究
Lancet Oncol. 2007 Aug;8(8):696-705. doi: 10.1016/S1470-2045(07)70208-5.
9
Timing of adjuvant radiotherapy and treatment outcome in childhood ependymoma.儿童室管膜瘤辅助放疗的时机与治疗效果。
Pediatr Blood Cancer. 2014 Apr;61(4):606-11. doi: 10.1002/pbc.24820. Epub 2013 Oct 26.
10
Ependymal tumors in childhood.儿童室管膜瘤
Pediatr Blood Cancer. 2005 Sep;45(3):298-303. doi: 10.1002/pbc.20212.

引用本文的文献

1
Optimizing outcomes in intracranial ependymoma: a contemporary review.优化颅内室管膜瘤的治疗结果:当代综述
Front Oncol. 2025 Jun 10;15:1617169. doi: 10.3389/fonc.2025.1617169. eCollection 2025.
2
Recurrent parietal lobe supratentorial ependymoma, ZFTA fusion-positive, CNS WHO grade 3, with new dural and calvarial reactive changes in a child: illustrative case.复发性顶叶幕上室管膜瘤,ZFTA融合阳性,中枢神经系统WHO 3级,患儿出现新的硬脑膜和颅骨反应性改变:病例说明
J Neurosurg Case Lessons. 2025 Jun 23;9(25). doi: 10.3171/CASE25146.
3
Molecular Testing for the World Health Organization Classification of Central Nervous System Tumors: A Review.世界卫生组织中枢神经系统肿瘤分类的分子检测:综述
JAMA Oncol. 2025 Mar 1;11(3):317-328. doi: 10.1001/jamaoncol.2024.5506.
4
Ependymoma from Benign to Highly Aggressive Diseases: A Review.从良性到高度侵袭性疾病的室管膜瘤:综述。
Adv Tech Stand Neurosurg. 2024;50:31-62. doi: 10.1007/978-3-031-53578-9_2.
5
Patient- and xenograft-derived organoids recapitulate pediatric brain tumor features and patient treatments.患者和异种移植物衍生类器官重现了儿科脑肿瘤的特征和患者的治疗情况。
EMBO Mol Med. 2023 Dec 7;15(12):e18199. doi: 10.15252/emmm.202318199. Epub 2023 Nov 30.
6
Outcomes after first relapse of children with intracranial ependymoma treated on the second l'Associazione Italiana di Ematologia e Oncologia Pediatrica (AIEOP) protocol.按照意大利儿科血液学和肿瘤学协会(AIEOP)方案治疗的颅内室管膜瘤患儿首次复发后的结局。
Neuro Oncol. 2022 Mar 12;24(3):480-481. doi: 10.1093/neuonc/noab297.

本文引用的文献

1
Ultra high-risk PFA ependymoma is characterized by loss of chromosome 6q.超高危 PFA 室管膜瘤的特征是染色体 6q 的缺失。
Neuro Oncol. 2021 Aug 2;23(8):1360-1370. doi: 10.1093/neuonc/noab034.
2
Outcomes after first relapse of childhood intracranial ependymoma.儿童颅内室管膜瘤首次复发后的结局
Pediatr Blood Cancer. 2021 Aug;68(8):e28930. doi: 10.1002/pbc.28930. Epub 2021 Feb 9.
3
Local and systemic therapy of recurrent ependymoma in children and adolescents: short- and long-term results of the E-HIT-REZ 2005 study.儿童和青少年复发性室管膜瘤的局部和全身治疗:E-HIT-REZ 2005 研究的短期和长期结果。
Neuro Oncol. 2021 Jun 1;23(6):1012-1023. doi: 10.1093/neuonc/noaa276.
4
Second series by the Italian Association of Pediatric Hematology and Oncology of children and adolescents with intracranial ependymoma: an integrated molecular and clinical characterization with a long-term follow-up.意大利儿童血液学和肿瘤学协会关于儿童和青少年颅内室管膜瘤的第二项研究系列:一项长期随访的综合分子与临床特征分析
Neuro Oncol. 2021 May 5;23(5):848-857. doi: 10.1093/neuonc/noaa257.
5
A retrospective analysis of recurrent pediatric ependymoma reveals extremely poor survival and ineffectiveness of current treatments across central nervous system locations and molecular subgroups.回顾性分析复发性小儿室管膜瘤显示,目前的治疗方法在中枢神经系统位置和分子亚群中均疗效甚微,患儿生存率极差。
Pediatr Blood Cancer. 2020 Sep;67(9):e28426. doi: 10.1002/pbc.28426. Epub 2020 Jul 2.
6
A systematic review and meta-analysis of outcomes in pediatric, recurrent ependymoma.小儿复发性室管膜瘤结局的系统评价和荟萃分析。
J Neurooncol. 2019 Sep;144(3):445-452. doi: 10.1007/s11060-019-03255-3. Epub 2019 Sep 9.
7
Re-irradiation of locally recurrent pediatric intracranial ependymoma: Experience of the French society of children's cancer.局部复发性小儿颅内室管膜瘤的再放疗:法国儿童癌症协会的经验。
Radiother Oncol. 2019 Mar;132:1-7. doi: 10.1016/j.radonc.2018.11.009. Epub 2018 Dec 20.
8
Conformal Radiation Therapy for Pediatric Ependymoma, Chemotherapy for Incompletely Resected Ependymoma, and Observation for Completely Resected, Supratentorial Ependymoma.儿童室管膜瘤的适形放疗、未完全切除的室管膜瘤的化疗和完全切除的、幕上室管膜瘤的观察。
J Clin Oncol. 2019 Apr 20;37(12):974-983. doi: 10.1200/JCO.18.01765. Epub 2019 Feb 27.
9
Craniospinal irradiation as part of re-irradiation for children with recurrent intracranial ependymoma.颅脊髓放疗作为复发性颅内室管膜瘤患儿再放疗的一部分。
Neuro Oncol. 2019 Mar 18;21(4):547-557. doi: 10.1093/neuonc/noy191.
10
Pediatric ependymoma: current treatment and newer therapeutic insights.小儿室管膜瘤:当前的治疗方法和新的治疗见解。
Future Oncol. 2018 Dec;14(30):3175-3186. doi: 10.2217/fon-2018-0502. Epub 2018 Nov 12.

2 项 AIEOP 方案中初次复发后颅内室管膜瘤的治疗和结果。

Treatment and outcome of intracranial ependymoma after first relapse in the 2nd AIEOP protocol.

机构信息

Pediatric Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Medical Statistics, Biometry and Bioinformatics Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

出版信息

Neuro Oncol. 2022 Mar 12;24(3):467-479. doi: 10.1093/neuonc/noab230.

DOI:10.1093/neuonc/noab230
PMID:
34605902
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8917409/
Abstract

BACKGROUND

More than 40% of patients with intracranial ependymoma need a salvage treatment within 5 years after diagnosis, and no standard treatment is available as yet. We report the outcome after first relapse of 64 patients treated within the 2nd AIEOP protocol.

METHODS

We considered relapse sites and treatments, that is, various combinations of complete/incomplete surgery, if followed by standard or hypofractionated radiotherapy (RT) ± chemotherapy (CT). Molecular analyses were available for 38/64 samples obtained at first diagnosis. Of the 64 cases, 55 were suitable for subsequent analyses.

RESULTS

The median follow-up was 147 months after diagnosis, 84 months after first relapse, 5-year EFS/OS were 26.2%/30.8% (median EFS/OS 13/32 months) after relapse. For patients with a local relapse (LR), the 5-year cumulative incidence of second LRs was 51.6%, with a 5-year event-specific probability of being LR-free of 40.0%. Tumor site/grade, need for shunting, age above/below 3 years, molecular subgroup at diagnosis, had no influence on outcomes. Due to variation in the RT dose/fractionation used and the subgroup sizes, it was not possible to assess the impact of the different RT modalities. Multivariable analyses identified completion of surgery, the absence of symptoms at relapse, and female sex as prognostically favorable. Tumors with a 1q gain carried a higher cumulative incidence of dissemination after first relapse.

CONCLUSIONS

Survival after recurrence was significantly influenced by symptoms and completeness of surgery. Only a homogeneous protocol with well-posed, randomized questions could clarify the numerous issues, orient salvage treatment, and ameliorate prognosis for this group of patients.

摘要

背景

超过 40%的颅内室管膜瘤患者在诊断后 5 年内需要进行挽救性治疗,但目前尚无标准治疗方法。我们报告了在第 2 个 AIEOP 方案中治疗的 64 例患者首次复发后的结果。

方法

我们考虑了复发部位和治疗方法,即各种完全/不完全手术的组合,如果随后进行标准或低分割放疗(RT)±化疗(CT)。在首次诊断时获得的 38/64 个样本中进行了分子分析。在 64 例病例中,有 55 例适合进行后续分析。

结果

中位随访时间为诊断后 147 个月,首次复发后 84 个月,复发后 5 年 EFS/OS 为 26.2%/30.8%(中位 EFS/OS 为 13/32 个月)。对于局部复发(LR)患者,5 年内第二次 LR 的累积发生率为 51.6%,无 LR 事件的 5 年特异性概率为 40.0%。肿瘤部位/分级、分流需求、年龄大于/小于 3 岁、诊断时的分子亚组对结局无影响。由于 RT 剂量/分割的变化和亚组大小的不同,无法评估不同 RT 方式的影响。多变量分析确定了手术的完成、复发时无症状以及女性是预后良好的因素。首次复发后,携带 1q 增益的肿瘤具有更高的传播累积发生率。

结论

复发后的生存受到症状和手术完整性的显著影响。只有具有明确、随机问题的同质方案才能阐明众多问题,为这组患者确定挽救性治疗方案并改善预后。