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循环肿瘤 DNA 血液生物标志物用于癌症早期检测的证据基础:系统绘图综述。

The evidence base for circulating tumour DNA blood-based biomarkers for the early detection of cancer: a systematic mapping review.

机构信息

WHO Classification of Tumours Group, International Agency for Research on Cancer (IARC), World Health Organization, 150 Cours Albert Thomas, 69372, Lyon, CEDEX 08, France.

Faculty of Health and Life Sciences, Coventry University, Priory Street, Coventry, CV1 5FB, UK.

出版信息

BMC Cancer. 2017 Oct 23;17(1):697. doi: 10.1186/s12885-017-3693-7.

Abstract

BACKGROUND

The presence of circulating cell-free DNA from tumours in blood (ctDNA) is of major importance to those interested in early cancer detection, as well as to those wishing to monitor tumour progression or diagnose the presence of activating mutations to guide treatment. In 2014, the UK Early Cancer Detection Consortium undertook a systematic mapping review of the literature to identify blood-based biomarkers with potential for the development of a non-invasive blood test for cancer screening, and which identified this as a major area of interest. This review builds on the mapping review to expand the ctDNA dataset to examine the best options for the detection of multiple cancer types.

METHODS

The original mapping review was based on comprehensive searches of the electronic databases Medline, Embase, CINAHL, the Cochrane library, and Biosis to obtain relevant literature on blood-based biomarkers for cancer detection in humans (PROSPERO no. CRD42014010827). The abstracts for each paper were reviewed to determine whether validation data were reported, and then examined in full. Publications concentrating on monitoring of disease burden or mutations were excluded.

RESULTS

The search identified 94 ctDNA studies meeting the criteria for review. All but 5 studies examined one cancer type, with breast, colorectal and lung cancers representing 60% of studies. The size and design of the studies varied widely. Controls were included in 77% of publications. The largest study included 640 patients, but the median study size was 65 cases and 35 controls, and the bulk of studies (71%) included less than 100 patients. Studies either estimated cfDNA levels non-specifically or tested for cancer-specific mutations or methylation changes (the majority using PCR-based methods).

CONCLUSION

We have systematically reviewed ctDNA blood biomarkers for the early detection of cancer. Pre-analytical, analytical, and post-analytical considerations were identified which need to be addressed before such biomarkers enter clinical practice. The value of small studies with no comparison between methods, or even the inclusion of controls is highly questionable, and larger validation studies will be required before such methods can be considered for early cancer detection.

摘要

背景

肿瘤细胞游离 DNA (ctDNA)在血液中的存在对那些热衷于早期癌症检测的人以及那些希望监测肿瘤进展或诊断激活突变以指导治疗的人具有重要意义。2014 年,英国早期癌症检测联合会进行了系统的文献图谱综述,以确定具有开发非侵入性血液癌症筛查测试潜力的血液生物标志物,并将其确定为一个主要关注领域。本综述在此图谱综述的基础上扩展了 ctDNA 数据集,以研究用于检测多种癌症类型的最佳选择。

方法

原始的图谱综述基于对电子数据库 Medline、Embase、CINAHL、Cochrane 图书馆和 Biosis 的全面搜索,以获取有关人类血液癌症检测生物标志物的相关文献(PROSPERO 编号:CRD42014010827)。综述了每篇论文的摘要,以确定是否报告了验证数据,然后进行了全面检查。排除了专注于监测疾病负担或突变的出版物。

结果

搜索共确定了符合综述标准的 94 项 ctDNA 研究。除了 5 项研究外,所有研究都检查了一种癌症类型,乳腺癌、结直肠癌和肺癌占研究的 60%。研究的规模和设计差异很大。77%的出版物包含了对照组。最大的研究纳入了 640 名患者,但中位研究规模为 65 例和 35 例对照,大部分研究(71%)纳入的患者少于 100 名。研究要么非特异性地估计 cfDNA 水平,要么检测癌症特异性突变或甲基化变化(大多数使用基于 PCR 的方法)。

结论

我们系统地综述了用于癌症早期检测的 ctDNA 血液生物标志物。在这些生物标志物进入临床实践之前,需要解决分析前、分析中和分析后考虑因素。没有方法之间比较甚至不包含对照组的小型研究的价值是非常值得怀疑的,在这些方法可以考虑用于早期癌症检测之前,需要进行更大的验证研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8573/5654013/903b634c9872/12885_2017_3693_Fig1_HTML.jpg

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