• 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

手术治疗局限性神经母细胞瘤:一项儿科肿瘤学组研究

Localized neuroblastoma treated by surgery: a Pediatric Oncology Group Study.

作者信息

Nitschke R, Smith E I, Shochat S, Altshuler G, Travers H, Shuster J J, Hayes F A, Patterson R, McWilliams N

机构信息

Oklahoma University Health Sciences Center, Oklahoma City.

出版信息

J Clin Oncol. 1988 Aug;6(8):1271-9. doi: 10.1200/JCO.1988.6.8.1271.

DOI:10.1200/JCO.1988.6.8.1271
PMID:3411339
Abstract

A prospective study was designed to evaluate the outcome of patients with localized resectable neuroblastoma without regional lymph node involvement when no therapy beyond surgical resection was administered. One hundred one patients observed for 3 to 60 months had a 2-year disease-free survival of 89% (SE = 5%). Of the nine patients experiencing relapse, only three have died. There were no apparent distinguishing characteristics of the nine failures. Due to the favorable prognosis of the subset of neuroblastoma patients, prognostic factor analysis had very limited power and lacked clinical importance. Complete gross removal of the localized tumors is adequate therapy to ensure the survival of the majority of these patients.

摘要

一项前瞻性研究旨在评估局限性可切除且无区域淋巴结受累的神经母细胞瘤患者,在未进行手术切除以外的治疗时的预后情况。101例患者接受了3至60个月的观察,其2年无病生存率为89%(标准误=5%)。在9例复发患者中,仅3例死亡。这9例治疗失败的患者没有明显的区别特征。由于该亚组神经母细胞瘤患者预后良好,预后因素分析的效能非常有限且缺乏临床重要性。对局限性肿瘤进行完整的肉眼切除是确保这些患者大多数存活的充分治疗方法。

相似文献

1
Localized neuroblastoma treated by surgery: a Pediatric Oncology Group Study.手术治疗局限性神经母细胞瘤:一项儿科肿瘤学组研究
J Clin Oncol. 1988 Aug;6(8):1271-9. doi: 10.1200/JCO.1988.6.8.1271.
2
N-Myc gene amplification is a major prognostic factor in localized neuroblastoma: results of the French NBL 90 study. Neuroblastoma Study Group of the Société Francaise d'Oncologie Pédiatrique.N-Myc基因扩增是局限性神经母细胞瘤的主要预后因素:法国NBL 90研究结果。法国儿科肿瘤学会神经母细胞瘤研究组。
J Clin Oncol. 1997 Mar;15(3):1171-82. doi: 10.1200/JCO.1997.15.3.1171.
3
Localized pelvic neuroblastoma: excellent survival and low morbidity with tailored therapy--the 10-year experience of the French Society of Pediatric Oncology.局限性盆腔神经母细胞瘤:个体化治疗带来优异生存率和低发病率——法国儿科肿瘤学会的10年经验
J Clin Oncol. 2004 May 1;22(9):1689-95. doi: 10.1200/JCO.2004.04.069.
4
Postoperative treatment of nonmetastatic visible residual neuroblastoma: a Pediatric Oncology Group study.非转移性可见残留神经母细胞瘤的术后治疗:一项儿科肿瘤学组的研究。
J Clin Oncol. 1991 Jul;9(7):1181-8. doi: 10.1200/JCO.1991.9.7.1181.
5
Infants with neuroblastoma and regional lymph node metastases have a favorable outlook after limited postoperative chemotherapy: a Pediatric Oncology Group study.
J Clin Oncol. 1992 Aug;10(8):1299-304. doi: 10.1200/JCO.1992.10.8.1299.
6
Radiotherapy improves the outlook for patients older than 1 year with Pediatric Oncology Group stage C neuroblastoma.放射治疗改善了1岁以上患有儿童肿瘤学组C期神经母细胞瘤患者的预后。
J Clin Oncol. 1991 May;9(5):789-95. doi: 10.1200/JCO.1991.9.5.789.
7
Localized resectable neuroblastoma: results of the second study of the Italian Cooperative Group for Neuroblastoma.局限性可切除神经母细胞瘤:意大利神经母细胞瘤协作组第二项研究结果
J Clin Oncol. 1995 Apr;13(4):884-93. doi: 10.1200/JCO.1995.13.4.884.
8
Biologic variables in the outcome of stages I and II neuroblastoma treated with surgery as primary therapy: a children's cancer group study.以手术作为主要治疗手段的I期和II期神经母细胞瘤治疗结果中的生物学变量:一项儿童癌症研究组的研究
J Clin Oncol. 2000 Jan;18(1):18-26. doi: 10.1200/JCO.2000.18.1.18.
9
Localized infant neuroblastomas often show spontaneous regression: results of the prospective trials NB95-S and NB97.局限性婴儿神经母细胞瘤常表现出自发性消退:前瞻性试验NB95-S和NB97的结果
J Clin Oncol. 2008 Mar 20;26(9):1504-10. doi: 10.1200/JCO.2007.12.3349.
10
Neuroblastoma.神经母细胞瘤
Saudi Med J. 2001 Aug;22(8):674-80.

引用本文的文献

1
Horner syndrome in a pediatric patient.一名儿科患者的霍纳综合征
Pediatr Investig. 2025 Feb 14;9(2):167-171. doi: 10.1002/ped4.12470. eCollection 2025 Jun.
2
Impact of risk-based therapy on late morbidity and mortality in neuroblastoma survivors: a report from the Childhood Cancer Survivor Study.基于风险的治疗对神经母细胞瘤幸存者晚期发病率和死亡率的影响:来自儿童癌症幸存者研究的报告。
J Natl Cancer Inst. 2024 Jun 7;116(6):885-894. doi: 10.1093/jnci/djae062.
3
International Society of Paediatric Surgical Oncology (IPSO) Surgical Practice Guidelines.
国际小儿外科肿瘤学会(IPSO)手术实践指南
Ecancermedicalscience. 2022 Feb 17;16:1356. doi: 10.3332/ecancer.2022.1356. eCollection 2022.
4
Long-Term Outcome and Role of Biology within Risk-Adapted Treatment Strategies: The Austrian Neuroblastoma Trial A-NB94.长期预后及生物学因素在风险适应性治疗策略中的作用:奥地利神经母细胞瘤试验A-NB94
Cancers (Basel). 2021 Feb 2;13(3):572. doi: 10.3390/cancers13030572.
5
The MDM2 inhibitor CGM097 combined with the BET inhibitor OTX015 induces cell death and inhibits tumor growth in models of neuroblastoma.MDM2 抑制剂 CGM097 联合 BET 抑制剂 OTX015 可诱导神经母细胞瘤模型中的细胞死亡并抑制肿瘤生长。
Cancer Med. 2020 Nov;9(21):8144-8158. doi: 10.1002/cam4.3407. Epub 2020 Oct 9.
6
Horner syndrome: clinical perspectives.霍纳综合征:临床视角
Eye Brain. 2015 Apr 10;7:35-46. doi: 10.2147/EB.S63633. eCollection 2015.
7
Revealed: The spy who regulates neuroblastoma stem cells.揭秘:调控神经母细胞瘤干细胞的“间谍”。
Oncotarget. 2014 Nov 30;5(22):11014-6. doi: 10.18632/oncotarget.2839.
8
A prospective study of expectant observation as primary therapy for neuroblastoma in young infants: a Children's Oncology Group study.一项针对小婴儿神经母细胞瘤期待观察作为一线治疗的前瞻性研究:一项儿童肿瘤协作组研究。
Ann Surg. 2012 Oct;256(4):573-80. doi: 10.1097/SLA.0b013e31826cbbbd.
9
Cancer stem cells: impact, heterogeneity, and uncertainty.癌症干细胞:影响、异质性和不确定性。
Cancer Cell. 2012 Mar 20;21(3):283-96. doi: 10.1016/j.ccr.2012.03.003.
10
Ganglioneuroblastoma of the posterior mediastinum: a case report.后纵隔神经节神经母细胞瘤:一例报告
J Med Case Rep. 2011 Jul 22;5:322. doi: 10.1186/1752-1947-5-322.