• 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

在 2 个独立队列中鉴定食管腺癌的预后表型。

Identification of Prognostic Phenotypes of Esophageal Adenocarcinoma in 2 Independent Cohorts.

机构信息

Divisions of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.

Medical Research Council Cancer Unit, Hutchison/Medical Research Council Research Centre, University of Cambridge, Cambridge, United Kingdom; European Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Hinxton, United Kingdom.

出版信息

Gastroenterology. 2018 Dec;155(6):1720-1728.e4. doi: 10.1053/j.gastro.2018.08.036. Epub 2018 Aug 27.

DOI:10.1053/j.gastro.2018.08.036
PMID:30165050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6298575/
Abstract

BACKGROUND & AIMS: Most patients with esophageal adenocarcinoma (EAC) present with de novo tumors. Although this could be due to inadequate screening strategies, the precise reason for this observation is not clear. We compared survival of patients with prevalent EAC with and without synchronous Barrett esophagus (BE) with intestinal metaplasia (IM) at the time of EAC diagnosis.

METHODS

Clinical data were studied using Cox proportional hazards regression to evaluate the effect of synchronous BE-IM on EAC survival independent of age, sex, TNM stage, and tumor location. We analyzed data from a cohort of patients with EAC from the Mayo Clinic (n=411; 203 with BE and IM) and a multicenter cohort from the United Kingdom (n=1417; 638 with BE and IM).

RESULTS

In the Mayo cohort, BE with IM had a reduced risk of death compared to patients without BE and IM (hazard ratio [HR] 0.44; 95% CI, 0.34-0.57; P<.001). In a multivariable analysis, BE with IM was associated with longer survival independent of patient age or sex, tumor stage or location, and BE length (adjusted HR, 0.66; 95% CI, 0.5-0.88; P=.005). In the United Kingdom cohort, patients BE and IM had a reduced risk of death compared with those without (HR, 0.59; 95% CI, 0.5-0.69; P<.001), with continued significance in multivariable analysis that included patient age and sex and tumor stage and tumor location (adjusted HR, 0.77; 95% CI, 0.64-0.93; P=.006).

CONCLUSION

Two types of EAC can be characterized based on the presence or absence of BE. These findings could increase our understanding the etiology of EAC, and be used in management and prognosis of patients.

摘要

背景与目的

大多数食管腺癌(EAC)患者表现为新发肿瘤。尽管这可能是由于筛查策略不足所致,但确切原因尚不清楚。我们比较了同时存在 EAC 时伴或不伴同步 Barrett 食管(BE)和肠上皮化生(IM)的患者的生存情况。

方法

使用 Cox 比例风险回归分析临床数据,以评估同步 BE-IM 对 EAC 生存的影响,该影响独立于年龄、性别、TNM 分期和肿瘤位置。我们分析了来自梅奥诊所的 EAC 患者队列(n=411;203 例伴 BE 和 IM)和来自英国的多中心队列(n=1417;638 例伴 BE 和 IM)的数据。

结果

在 Mayo 队列中,与无 BE 和 IM 的患者相比,同时存在 BE 和 IM 的患者死亡风险降低(风险比 [HR] 0.44;95%CI,0.34-0.57;P<.001)。在多变量分析中,独立于患者年龄或性别、肿瘤分期或部位以及 BE 长度,同时存在 BE 和 IM 与更长的生存相关(调整后的 HR,0.66;95%CI,0.5-0.88;P=.005)。在英国队列中,与无 BE 和 IM 的患者相比,同时存在 BE 和 IM 的患者死亡风险降低(HR,0.59;95%CI,0.5-0.69;P<.001),在包括患者年龄和性别以及肿瘤分期和肿瘤位置的多变量分析中仍然具有显著意义(调整后的 HR,0.77;95%CI,0.64-0.93;P=.006)。

结论

可以根据是否存在 BE 来描述两种类型的 EAC。这些发现可以增加我们对 EAC 病因的理解,并用于患者的管理和预后。

相似文献

1
Identification of Prognostic Phenotypes of Esophageal Adenocarcinoma in 2 Independent Cohorts.在 2 个独立队列中鉴定食管腺癌的预后表型。
Gastroenterology. 2018 Dec;155(6):1720-1728.e4. doi: 10.1053/j.gastro.2018.08.036. Epub 2018 Aug 27.
2
Cytokeratin expression patterns in noncardia, intestinal metaplasia-associated gastric adenocarcinoma: implication for the evaluation of intestinal metaplasia and tumors at the esophagogastric junction.非贲门部肠化生相关胃腺癌中的细胞角蛋白表达模式:对食管胃交界部肠化生及肿瘤评估的意义
Cancer. 2002 Feb 1;94(3):820-31. doi: 10.1002/cncr.10215.
3
Young Adults With Esophageal Adenocarcinoma Present With More Advanced Stage Tumors and Have Shorter Survival Times.青年食管腺癌患者的肿瘤分期更晚,生存时间更短。
Clin Gastroenterol Hepatol. 2019 Aug;17(9):1756-1762. doi: 10.1016/j.cgh.2018.09.031. Epub 2018 Sep 27.
4
Comparison of cancer-associated genetic abnormalities in columnar-lined esophagus tissues with and without goblet cells.比较有和无杯状细胞的柱状上皮食管组织中的癌相关遗传异常。
Ann Surg. 2014 Jul;260(1):72-80. doi: 10.1097/SLA.0000000000000424.
5
Prognostic Impact of the Presence of Barrett's Esophagus and Intestinal Metaplasia on Esophageal Adenocarcinoma Survival.巴雷特食管和肠化生的存在对食管腺癌生存的预后影响
Foregut. 2022 Dec;2(4):356-364. doi: 10.1177/26345161211033277. Epub 2021 Aug 20.
6
Esophageal adenocarcinoma phenotypes and risk factors.食管腺癌表型及危险因素。
Curr Opin Gastroenterol. 2022 Jul 1;38(4):423-427. doi: 10.1097/MOG.0000000000000844.
7
Presence or absence of intestinal metaplasia but not its burden is associated with prevalent high-grade dysplasia and cancer in Barrett's esophagus.肠化生的有无而非其程度与巴雷特食管中现患的高级别异型增生和癌症相关。
Dis Esophagus. 2014 Nov-Dec;27(8):751-6. doi: 10.1111/dote.12151. Epub 2013 Oct 28.
8
Association of Biomarkers for Human Papillomavirus With Survival Among Adults With Barrett High-grade Dysplasia and Esophageal Adenocarcinoma.人乳头瘤病毒生物标志物与 Barrett 高级别异型增生和食管腺癌成人患者生存的关联。
JAMA Netw Open. 2020 Feb 5;3(2):e1921189. doi: 10.1001/jamanetworkopen.2019.21189.
9
High Expression of Cathepsin E in Tissues but Not Blood of Patients with Barrett's Esophagus and Adenocarcinoma.组织蛋白酶E在巴雷特食管和腺癌患者的组织而非血液中高表达。
Ann Surg Oncol. 2015 Jul;22(7):2431-8. doi: 10.1245/s10434-014-4155-y. Epub 2014 Oct 28.
10
Esophageal pepsin and proton pump synthesis in barrett's esophagus and esophageal adenocarcinoma.巴雷特食管和食管腺癌中的食管胃蛋白酶和质子泵合成。
Laryngoscope. 2019 Dec;129(12):2687-2695. doi: 10.1002/lary.28051. Epub 2019 May 2.

引用本文的文献

1
Detection of Barrett's Esophagus Prior to Development of Esophageal and Esophagogastric Junction Adenocarcinoma.食管及食管胃交界腺癌发生前Barrett食管的检测
Clin Gastroenterol Hepatol. 2025 Apr 30. doi: 10.1016/j.cgh.2025.02.016.
2
Adenocarcinoma of the esophagogastric junction: characteristics of female patients and young adult patients based on a 12-year retrospective and prospective multicenter clinicoepidemiological cohort study in Japan.食管胃交界腺癌:基于日本一项为期12年的回顾性和前瞻性多中心临床流行病学队列研究的女性患者和年轻成年患者特征
BMC Gastroenterol. 2024 Oct 1;24(1):342. doi: 10.1186/s12876-024-03421-6.
3

本文引用的文献

1
Long-term survival based on pathologic response to neoadjuvant therapy in esophageal cancer.基于食管癌新辅助治疗病理反应的长期生存情况
J Surg Res. 2017 Aug;216:65-72. doi: 10.1016/j.jss.2017.03.022. Epub 2017 Mar 31.
2
The Evolving Genomic Landscape of Barrett's Esophagus and Esophageal Adenocarcinoma.巴雷特食管和食管腺癌不断演变的基因组格局
Gastroenterology. 2017 Sep;153(3):657-673.e1. doi: 10.1053/j.gastro.2017.07.007. Epub 2017 Jul 14.
3
Alternatives to Traditional Per-Oral Endoscopy for Screening.用于筛查的传统经口内镜检查的替代方法。
p53 mutation biases squamocolumnar junction progenitor cells towards dysplasia rather than metaplasia in Barrett's oesophagus.
在巴雷特食管中,p53突变使鳞柱状交界祖细胞倾向于发育异常而非化生。
Gut. 2025 Jan 17;74(2):182-196. doi: 10.1136/gutjnl-2024-332095.
4
Gastro-Esophageal Junction Precancerosis: Histological Diagnostic Approach and Pathogenetic Insights.胃食管交界部癌前病变:组织学诊断方法及发病机制见解
Cancers (Basel). 2023 Dec 6;15(24):5725. doi: 10.3390/cancers15245725.
5
Molecular Biology and Clinical Management of Esophageal Adenocarcinoma.食管腺癌的分子生物学与临床管理
Cancers (Basel). 2023 Nov 14;15(22):5410. doi: 10.3390/cancers15225410.
6
Understanding the malignant potential of gastric metaplasia of the oesophagus and its relevance to Barrett's oesophagus surveillance: individual-level data analysis.了解食管胃型化生的恶性潜能及其与 Barrett 食管监测的相关性:个体水平数据分析。
Gut. 2024 Apr 5;73(5):729-740. doi: 10.1136/gutjnl-2023-330721.
7
Esophageal organoids: applications and future prospects.食管类器官:应用与未来前景。
J Mol Med (Berl). 2023 Aug;101(8):931-945. doi: 10.1007/s00109-023-02340-5. Epub 2023 Jun 29.
8
Improving outcomes in patients with oesophageal cancer.改善食管癌患者的预后。
Nat Rev Clin Oncol. 2023 Jun;20(6):390-407. doi: 10.1038/s41571-023-00757-y. Epub 2023 Apr 21.
9
Cancer Risk in Barrett's Esophagus: A Clinical Review.巴雷特食管中的癌症风险:临床综述。
Int J Mol Sci. 2023 Mar 23;24(7):6018. doi: 10.3390/ijms24076018.
10
Current Status and Future Prospects for Esophageal Cancer.食管癌的现状与未来展望
Cancers (Basel). 2023 Jan 26;15(3):765. doi: 10.3390/cancers15030765.
Gastrointest Endosc Clin N Am. 2017 Jul;27(3):379-396. doi: 10.1016/j.giec.2017.02.002. Epub 2017 Apr 4.
4
Cancer of the esophagus and esophagogastric junction-Major changes in the American Joint Committee on Cancer eighth edition cancer staging manual.食管癌和食管胃交界癌——美国癌症联合委员会第八版癌症分期手册的重大变化。
CA Cancer J Clin. 2017 Jul 8;67(4):304-317. doi: 10.3322/caac.21399. Epub 2017 May 26.
5
Risk of oesophageal adenocarcinoma in individuals with Barrett's oesophagus.巴雷特食管患者发生食管腺癌的风险。
Eur J Cancer. 2017 Apr;75:41-46. doi: 10.1016/j.ejca.2016.12.037. Epub 2017 Feb 17.
6
Corrigendum: Mutational signatures in esophageal adenocarcinoma define etiologically distinct subgroups with therapeutic relevance.勘误:食管腺癌中的突变特征定义了具有治疗相关性的病因学上不同的亚组。
Nat Genet. 2017 Jan 31;49(2):317. doi: 10.1038/ng0217-317a.
7
Systematic review with meta-analysis: prevalent vs. incident oesophageal adenocarcinoma and high-grade dysplasia in Barrett's oesophagus.系统评价与荟萃分析:巴雷特食管中食管腺癌和高级别异型增生的患病率与发病率对比
Aliment Pharmacol Ther. 2016 Oct;44(8):775-84. doi: 10.1111/apt.13783. Epub 2016 Aug 26.
8
Trends in esophageal cancer survival in United States adults from 1973 to 2009: A SEER database analysis.1973年至2009年美国成年人食管癌生存率趋势:一项监测、流行病学和最终结果(SEER)数据库分析
J Gastroenterol Hepatol. 2016 Jun;31(6):1141-6. doi: 10.1111/jgh.13289.
9
A Systematic Review of Esophageal MicroRNA Markers for Diagnosis and Monitoring of Barrett's Esophagus.用于巴雷特食管诊断和监测的食管微小RNA标志物的系统评价
Dig Dis Sci. 2016 Apr;61(4):1039-50. doi: 10.1007/s10620-015-3959-3. Epub 2015 Nov 14.
10
Surveillance endoscopy is associated with improved outcomes of oesophageal adenocarcinoma detected in patients with Barrett's oesophagus.监测内镜检查与 Barrett 食管患者中检测到的食管腺癌的改善结局相关。
Gut. 2016 Aug;65(8):1252-60. doi: 10.1136/gutjnl-2014-308865. Epub 2015 Aug 26.