• 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

探索儿童神经母细胞瘤:美国肾上腺和非肾上腺肿瘤特征的综合分析

Exploring Pediatric Neuroblastoma: A Comprehensive Analysis of Adrenal and Nonadrenal Tumor Characteristics in the United States.

作者信息

AlWawi Ghaith, Alrefai Mohammad Omar, Al-Wawi Mohd Zaki, Qasim Asma, Hammami M Bakri

机构信息

Department of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.

Department of Nephrology, Mayo Clinic, Rochester, Minnesota, United States.

出版信息

Avicenna J Med. 2025 Apr 2;15(1):1-8. doi: 10.1055/s-0045-1807243. eCollection 2025 Jan.

DOI:10.1055/s-0045-1807243
PMID:40395697
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12088804/
Abstract

BACKGROUND AND PURPOSE

Neuroblastoma (NB) is an aggressive malignant tumor arising from a primitive neural crest origin. While the significance of tumor location in survival outcomes is recognized, it remains inadequately explored. This study provides a comprehensive analysis of the survival and characteristics of pediatric adrenal and nonadrenal NBs in the United States.

METHODS

A retrospective analysis of pediatric primary NB between 1975 and 2016 was conducted using the Surveillance, Epidemiology, and End Results (SEER) database. Univariate and multivariate regression analyses were used to determine prognostic variables.

RESULTS

A total of 4,554 patients were included, comprising 52% males (  = 2,385) and 79.2% Caucasians (  = 3,569). The median age of the patients was one year (range: 0-19 years). In all, 44.4% (  = 1,996) of the patients had adrenal NB and 55.6% (  = 2,496) patients had nonadrenal NB. Adrenal NB was significantly more prevalent among males and those presenting at a younger age (  < 0.001). Adrenal NB was more likely to have a higher grade and distant metastasis at diagnosis (  < 0.001). Nonadrenal NB, female sex, surgical resection, and later year of diagnosis were associated with improved survival (  < 0.001).

CONCLUSION

This study highlights important factors that are helpful for prognostication of NB patients in the United States. Tailored approaches considering tumor site are crucial for effective management of NB.

摘要

背景与目的

神经母细胞瘤(NB)是一种起源于原始神经嵴的侵袭性恶性肿瘤。虽然肿瘤位置对生存结果的重要性已得到认可,但仍未得到充分研究。本研究对美国儿童肾上腺和非肾上腺NB的生存情况及特征进行了全面分析。

方法

使用监测、流行病学和最终结果(SEER)数据库对1975年至2016年间的儿童原发性NB进行回顾性分析。采用单因素和多因素回归分析来确定预后变量。

结果

共纳入4554例患者,其中男性占52%(n = 2385),白种人占79.2%(n = 3569)。患者的中位年龄为1岁(范围:0 - 19岁)。总体而言,44.4%(n = 1996)的患者患有肾上腺NB,55.6%(n = 2496)的患者患有非肾上腺NB。肾上腺NB在男性和年龄较小的患者中更为普遍(P < 0.001)。肾上腺NB在诊断时更有可能具有更高的分级和远处转移(P < 0.001)。非肾上腺NB、女性、手术切除和较晚的诊断年份与生存率提高相关(P < 0.001)。

结论

本研究强调了有助于美国NB患者预后评估的重要因素。考虑肿瘤部位的个性化治疗方法对于NB的有效管理至关重要。

相似文献

1
Exploring Pediatric Neuroblastoma: A Comprehensive Analysis of Adrenal and Nonadrenal Tumor Characteristics in the United States.探索儿童神经母细胞瘤:美国肾上腺和非肾上腺肿瘤特征的综合分析
Avicenna J Med. 2025 Apr 2;15(1):1-8. doi: 10.1055/s-0045-1807243. eCollection 2025 Jan.
2
Pediatric Patients with Adrenal Neuroblastoma: A SEER Analysis, 2004-2013.2004 - 2013年肾上腺神经母细胞瘤儿科患者:监测、流行病学和最终结果(SEER)分析
Am Surg. 2020 Feb 1;86(2):127-133.
3
Clinical, biologic, and prognostic differences on the basis of primary tumor site in neuroblastoma: a report from the international neuroblastoma risk group project.神经母细胞瘤中原发肿瘤部位的临床、生物学及预后差异:国际神经母细胞瘤风险组项目报告
J Clin Oncol. 2014 Oct 1;32(28):3169-76. doi: 10.1200/JCO.2014.56.1621. Epub 2014 Aug 25.
4
Prognostic impact of tumor size on patients with neuroblastoma in a SEER-based study.基于 SEER 的研究:肿瘤大小对神经母细胞瘤患者预后的影响。
Cancer Med. 2022 Jul;11(14):2779-2789. doi: 10.1002/cam4.4653. Epub 2022 Mar 22.
5
Metastasis pattern and prognosis in children with neuroblastoma.神经母细胞瘤患儿的转移模式和预后。
World J Surg Oncol. 2023 Apr 12;21(1):130. doi: 10.1186/s12957-023-03011-y.
6
Clinical Characteristics and Survival Outcomes in Neuroblastoma With Bone Metastasis Based on SEER Database Analysis.基于监测、流行病学和最终结果(SEER)数据库分析的神经母细胞瘤骨转移的临床特征和生存结果
Front Oncol. 2021 Jun 1;11:677023. doi: 10.3389/fonc.2021.677023. eCollection 2021.
7
Recent advances in the developmental origin of neuroblastoma: an overview.神经母细胞瘤发生发展的最新研究进展:综述
J Exp Clin Cancer Res. 2022 Mar 11;41(1):92. doi: 10.1186/s13046-022-02281-w.
8
Individual risk and prognostic value prediction by interpretable machine learning for distant metastasis in neuroblastoma: A population-based study and an external validation.通过可解释机器学习预测神经母细胞瘤远处转移的个体风险和预后价值:一项基于人群的研究及外部验证
Int J Med Inform. 2025 Apr;196:105813. doi: 10.1016/j.ijmedinf.2025.105813. Epub 2025 Jan 29.
9
Establishment and validation of a nomogram to predict cancer-specific survival in pediatric neuroblastoma patients.用于预测小儿神经母细胞瘤患者癌症特异性生存的列线图的建立与验证
Front Pediatr. 2023 Mar 3;11:1105922. doi: 10.3389/fped.2023.1105922. eCollection 2023.
10
Feasible laparoscopic surgery for selected cases of primary adrenal neuroblastoma: Results from a comparison with open surgery at a single institution.选择病例行腹腔镜手术治疗原发性肾上腺神经母细胞瘤的可行性:来自单中心开放手术对比的结果。
Asian J Endosc Surg. 2023 Jul;16(3):473-481. doi: 10.1111/ases.13204. Epub 2023 May 23.

本文引用的文献

1
Approval of DFMO for high-risk neuroblastoma patients demonstrates a step of success to target MYC pathway.DFMO 获批用于高危神经母细胞瘤患者,标志着靶向 MYC 通路的一个成功步骤。
Br J Cancer. 2024 Mar;130(4):513-516. doi: 10.1038/s41416-024-02599-6. Epub 2024 Feb 5.
2
Neuroblastoma arises in early fetal development and its evolutionary duration predicts outcome.神经母细胞瘤发生于胎儿早期发育阶段,其进化持续时间可预测结局。
Nat Genet. 2023 Apr;55(4):619-630. doi: 10.1038/s41588-023-01332-y. Epub 2023 Mar 27.
3
Long-Term Survival of Neuroblastoma Patients Receiving Surgery, Chemotherapy, and Radiotherapy: A Propensity Score Matching Study.接受手术、化疗和放疗的神经母细胞瘤患者的长期生存:一项倾向评分匹配研究
J Clin Med. 2023 Jan 17;12(3):754. doi: 10.3390/jcm12030754.
4
Linking neural crest development to neuroblastoma pathology.将神经嵴发育与神经母细胞瘤病理联系起来。
Development. 2022 Aug 1;149(15). doi: 10.1242/dev.200331. Epub 2022 Jul 29.
5
High-Risk and Relapsed Neuroblastoma: Toward More Cures and Better Outcomes.高危神经母细胞瘤和复发性神经母细胞瘤:追求更高的治愈率和更好的预后。
Am Soc Clin Oncol Educ Book. 2022 Apr;42:1-13. doi: 10.1200/EDBK_349783.
6
Recent advances in the developmental origin of neuroblastoma: an overview.神经母细胞瘤发生发展的最新研究进展:综述
J Exp Clin Cancer Res. 2022 Mar 11;41(1):92. doi: 10.1186/s13046-022-02281-w.
7
MYCN Function in Neuroblastoma Development.MYCN在神经母细胞瘤发展中的作用。
Front Oncol. 2021 Jan 27;10:624079. doi: 10.3389/fonc.2020.624079. eCollection 2020.
8
Long-Term Follow-up of a Phase III Study of ch14.18 (Dinutuximab) + Cytokine Immunotherapy in Children with High-Risk Neuroblastoma: COG Study ANBL0032.高危神经母细胞瘤患儿中 ch14.18(dinutuximab)联合细胞因子免疫治疗的 III 期研究的长期随访:COG 研究 ANBL0032。
Clin Cancer Res. 2021 Apr 15;27(8):2179-2189. doi: 10.1158/1078-0432.CCR-20-3909. Epub 2021 Jan 27.
9
Comparison of Incidence and Outcomes of Neuroblastoma in Children, Adolescents, and Adults in the United States: A Surveillance, Epidemiology, and End Results (SEER) Program Population Study.美国儿童、青少年和成人神经母细胞瘤的发病率及预后比较:一项监测、流行病学和最终结果(SEER)计划人群研究。
Med Sci Monit. 2020 Nov 29;26:e927218. doi: 10.12659/MSM.927218.
10
The Association between Race and Survival among Pediatric Patients with Neuroblastoma in the US between 1973 and 2015.1973 年至 2015 年美国儿童神经母细胞瘤患者的种族与生存关系。
Int J Environ Res Public Health. 2020 Jul 15;17(14):5119. doi: 10.3390/ijerph17145119.