• 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

通用癌症筛查:具有革命性、合理性且切实可行。

Universal cancer screening: revolutionary, rational, and realizable.

作者信息

Ahlquist David A

机构信息

Mayo Clinic, Rochester, MN USA.

出版信息

NPJ Precis Oncol. 2018 Oct 29;2:23. doi: 10.1038/s41698-018-0066-x. eCollection 2018.

DOI:10.1038/s41698-018-0066-x
PMID:30393772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6206005/
Abstract

Cancer remains the second leading cause of mortality worldwide, and overall cancer-related deaths are increasing. Despite the survival benefit from early detection, screening has to date targeted only those few organs that harbor tumors of sufficient prevalence to show cost-effectiveness at population levels, leaving most cancer types unscreened. In this perspective overview, a case is made for universal cancer screening as a logical and more inclusive approach with potentially high impact. The centrally important conceptual drivers to universal screening are biological and epidemiological. The shared biology of tumor marker release into a common distant medium, like blood, can be exploited for multi-cancer detection from a single test. And, by aggregating prevalence rates, universal screening allows all cancers (including less common ones) to be included as targets, increases screening efficiency and integration across tumor types, and potentially improves cost-effectiveness over single-organ approaches. The identification of new tumor marker classes with both broad expression across tumor types and site-prediction, remarkable advances in assay technologies, and compelling early clinical data increase the likelihood of actualizing this new paradigm. Multi-organ screening could be achieved by targeting markers within or stemming from the circulation (including blood, urine, saliva, and expired breath) or those exfoliated into common excretory pathways (including the gastrointestinal and female reproductive tracts). Rigorous clinical studies in intended use populations and collaborations between academia, industry, professional societies, and government will be required to bring this lofty vision to a population application.

摘要

癌症仍然是全球第二大死因,且与癌症相关的总体死亡人数正在增加。尽管早期检测能带来生存益处,但迄今为止,筛查仅针对少数几个器官,这些器官中肿瘤的患病率足以在人群层面显示出成本效益,而大多数癌症类型仍未得到筛查。在这篇观点综述中,我们提出将通用癌症筛查作为一种合理且更具包容性、可能具有重大影响的方法。通用筛查的核心重要概念驱动因素是生物学和流行病学因素。肿瘤标志物释放到血液等共同的远处介质中的共同生物学特性,可用于通过单次检测进行多种癌症的检测。而且,通过汇总患病率,通用筛查可将所有癌症(包括不太常见的癌症)纳入目标范围,提高筛查效率以及跨肿瘤类型的整合度,并有可能比单一器官筛查方法提高成本效益。新型肿瘤标志物类别的识别,这些标志物在多种肿瘤类型中广泛表达且具有部位预测能力,检测技术的显著进步,以及引人注目的早期临床数据,增加了实现这一新模式的可能性。多器官筛查可以通过针对循环系统(包括血液、尿液、唾液和呼出气体)中或源自循环系统的标志物,或那些脱落到常见排泄途径(包括胃肠道和女性生殖道)中的标志物来实现。需要在目标使用人群中进行严格的临床研究,以及学术界、产业界、专业协会和政府之间的合作,才能将这一宏伟愿景应用于人群。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/939cb6a6c657/41698_2018_66_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/cb3949394a6f/41698_2018_66_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/047518e943a1/41698_2018_66_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/939cb6a6c657/41698_2018_66_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/cb3949394a6f/41698_2018_66_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/047518e943a1/41698_2018_66_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/303c/6206005/939cb6a6c657/41698_2018_66_Fig3_HTML.jpg

相似文献

1
Universal cancer screening: revolutionary, rational, and realizable.通用癌症筛查:具有革命性、合理性且切实可行。
NPJ Precis Oncol. 2018 Oct 29;2:23. doi: 10.1038/s41698-018-0066-x. eCollection 2018.
2
3
Overview of resistance to systemic therapy in patients with breast cancer.乳腺癌患者全身治疗耐药概述。
Adv Exp Med Biol. 2007;608:1-22. doi: 10.1007/978-0-387-74039-3_1.
4
5
Mammography screening: A major issue in medicine.乳腺 X 光筛查:医学中的一个重大问题。
Eur J Cancer. 2018 Feb;90:34-62. doi: 10.1016/j.ejca.2017.11.002. Epub 2017 Dec 20.
6
Sepsis Care Pathway 2019.2019年脓毒症护理路径
Qatar Med J. 2019 Nov 7;2019(2):4. doi: 10.5339/qmj.2019.qccc.4. eCollection 2019.
7
8
9
10
Cost-effectiveness analysis of lead poisoning screening strategies following the 1997 guidelines of the Centers for Disease Control and Prevention.遵循美国疾病控制与预防中心1997年指南的铅中毒筛查策略的成本效益分析。
Arch Pediatr Adolesc Med. 1998 Dec;152(12):1202-8. doi: 10.1001/archpedi.152.12.1202.

引用本文的文献

1
Multi-cancer Detection Using Pattern Formation in Drying Body Fluids: A Systematic Review and Meta-Analysis of Diagnostic Test Accuracy Studies.利用干燥体液中的模式形成进行多癌检测:诊断试验准确性研究的系统评价和荟萃分析
Technol Cancer Res Treat. 2025 Jan-Dec;24:15330338251333994. doi: 10.1177/15330338251333994. Epub 2025 Sep 1.
2
Liquid biopsy-based multi-cancer early detection: an exploration road from evidence to implementation.基于液体活检的多癌早期检测:从证据到实施的探索之路
Sci Bull (Beijing). 2025 Sep 15;70(17):2852-2867. doi: 10.1016/j.scib.2025.06.030. Epub 2025 Jun 24.
3
Incidental vs. symptomatic diagnosis of follicular lymphoma: implications of earlier detection.

本文引用的文献

1
Cancer screening in the United States, 2018: A review of current American Cancer Society guidelines and current issues in cancer screening.美国 2018 年癌症筛查:对当前美国癌症协会指南和癌症筛查中当前问题的综述。
CA Cancer J Clin. 2018 Jul;68(4):297-316. doi: 10.3322/caac.21446. Epub 2018 May 30.
2
Detection of Gastric Cancer with Novel Methylated DNA Markers: Discovery, Tissue Validation, and Pilot Testing in Plasma.新型甲基化 DNA 标志物检测胃癌:在组织中的验证及血浆的初步检测。
Clin Cancer Res. 2018 Nov 15;24(22):5724-5734. doi: 10.1158/1078-0432.CCR-17-3364. Epub 2018 May 29.
3
Early non-invasive detection of breast cancer using exhaled breath and urine analysis.
滤泡性淋巴瘤的偶然诊断与症状性诊断:早期检测的影响
Blood Cancer J. 2025 Jul 3;15(1):116. doi: 10.1038/s41408-025-01322-9.
4
Diagnostic value of the wnt target and cancer-associated blood biomarker hPG80: ONCOPRO case-control prospective study.Wnt靶标与癌症相关血液生物标志物hPG80的诊断价值:ONCOPRO病例对照前瞻性研究
Biomark Res. 2025 Jul 1;13(1):91. doi: 10.1186/s40364-025-00793-z.
5
Assessment of the impact of multi-cancer early detection test screening intervals on late-stage cancer at diagnosis and mortality using a state-transition model.使用状态转换模型评估多癌早期检测测试筛查间隔对诊断时晚期癌症和死亡率的影响。
BMJ Open. 2025 May 8;15(5):e086648. doi: 10.1136/bmjopen-2024-086648.
6
Clinical Evaluation of Cancer Signal Origin Prediction and Diagnostic Resolution following Multicancer Early Detection Testing in the PATHFINDER Study.PATHFINDER研究中多癌早期检测测试后癌症信号起源预测和诊断分辨率的临床评估
Cancer Prev Res (Phila). 2025 Aug 1;18(8):475-483. doi: 10.1158/1940-6207.CAPR-24-0468.
7
Navigating Complexity: Perspectives on Risk Assessment in the Era of New Blood-Based Tests for Early Cancer Detection.应对复杂性:早期癌症检测新型血液检测时代的风险评估视角
Clin Cancer Res. 2025 Jun 13;31(12):2267-2270. doi: 10.1158/1078-0432.CCR-24-4269.
8
Multicancer early detection testing: Guidance for primary care discussions with patients.多癌早期检测测试:与患者进行初级保健讨论的指南。
Cancer. 2025 Apr 1;131(7):e35823. doi: 10.1002/cncr.35823.
9
Estimating the Burden of False Positives and Implementation Costs From Adding Multiple Single Cancer Tests or a Single Multi-Cancer Test to Standard-Of-Care Screening.评估在标准护理筛查中增加多项单一癌症检测或一项多癌症检测所产生的假阳性负担和实施成本。
Cancer Med. 2025 Mar;14(6):e70776. doi: 10.1002/cam4.70776.
10
Are Non-invasive Multi-cancer Early Cancer Detection Tests the Future?非侵入性多癌早期癌症检测测试是未来的发展方向吗?
Dig Dis Sci. 2025 Jan 30. doi: 10.1007/s10620-024-08839-2.
使用呼气和尿液分析进行早期无创乳腺癌检测。
Comput Biol Med. 2018 May 1;96:227-232. doi: 10.1016/j.compbiomed.2018.04.002. Epub 2018 Apr 4.
4
Lung Cancer Screening, Version 3.2018, NCCN Clinical Practice Guidelines in Oncology.肺癌筛查,版本 3.2018,NCCN 肿瘤学临床实践指南。
J Natl Compr Canc Netw. 2018 Apr;16(4):412-441. doi: 10.6004/jnccn.2018.0020.
5
Cell-of-Origin Patterns Dominate the Molecular Classification of 10,000 Tumors from 33 Types of Cancer.起源细胞模式主导了 33 种癌症类型的 10000 个肿瘤的分子分类。
Cell. 2018 Apr 5;173(2):291-304.e6. doi: 10.1016/j.cell.2018.03.022.
6
Opportunities and obstacles for deep learning in biology and medicine.深度学习在生物学和医学中的机遇与挑战。
J R Soc Interface. 2018 Apr;15(141). doi: 10.1098/rsif.2017.0387.
7
Evaluation of liquid from the Papanicolaou test and other liquid biopsies for the detection of endometrial and ovarian cancers.巴氏涂片检查和其他液体活检测试在子宫内膜癌和卵巢癌检测中的评估。
Sci Transl Med. 2018 Mar 21;10(433). doi: 10.1126/scitranslmed.aap8793.
8
Detection and localization of surgically resectable cancers with a multi-analyte blood test.通过多分析物血液检测对外科可切除癌症进行检测和定位。
Science. 2018 Feb 23;359(6378):926-930. doi: 10.1126/science.aar3247. Epub 2018 Jan 18.
9
Cancer statistics, 2018.癌症统计数据,2018 年。
CA Cancer J Clin. 2018 Jan;68(1):7-30. doi: 10.3322/caac.21442. Epub 2018 Jan 4.
10
Unveiling massive numbers of cancer-related urinary-microRNA candidates via nanowires.通过纳米线揭示大量与癌症相关的尿 microRNA 候选物。
Sci Adv. 2017 Dec 15;3(12):e1701133. doi: 10.1126/sciadv.1701133. eCollection 2017 Dec.