胰腺癌中的DUPAN-2:系统回顾和荟萃分析。

IF 3.2 3区 医学 Q2 MEDICAL LABORATORY TECHNOLOGY Clinica Chimica Acta Pub Date : 2025-02-01 Epub Date: 2024-12-07 DOI:10.1016/j.cca.2024.120080
Xiaowen Gong, Yuerong Xuan, Chengshuai Pang, Chenyang Dong, Rui Cao, Zhigang Wei, Chaojie Liang
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引用次数: 0

摘要

目的:胰腺癌是一种预后差、死亡率高、侵袭性强的恶性肿瘤。迫切需要确定可靠的生物标志物以进行早期诊断和治疗。本研究旨在通过荟萃分析综合评价DUPAN-2在PC中的诊断和预后价值。方法:我们系统地检索PubMed、Embase和其他数据库中与DUPAN-2及其在PC中的预后和诊断相关性相关的研究,涵盖截至2024年8月的出版物。我们使用合并风险比(hr)评估DUPAN-2在PC中的预后价值,使用总受试者工作特征(SROC)曲线和曲线下面积(AUC)评估诊断效果,使用合并优势比(ORs)分析与临床病理特征的相关性。结果:本次荟萃分析共纳入22项研究,涉及4765例患者,其中11项研究集中于诊断分析,10项研究集中于预后分析,3项研究集中于临床病理特征。诊断荟萃分析显示,合并敏感性为0.63(95 % CI: 0.56-0.69),合并特异性为0.98(95 % CI: 0.95-0.99), AUC为0.83(95 % CI: 0.79-0.86)。亚组分析表明,DUPAN-2阈值在150 U/mL时达到最高诊断性能。预后荟萃分析显示,DUPAN-2水平升高与较差的OS (HR = 1.70,95 % CI: 1.36-2.14)和PFS (HR = 1.33,95 % CI: 1.14-1.56)相关。此外,临床病理特性分析表明,DUPAN-2水平升高与血管侵犯相关(或 = 3.48,95 % CI: 1.26 - -9.59),而规范化DUPAN-2水平与高resectability(或 = 0.57,95 % CI: 0.36 - -0.90)和低N-stage(或 = 0.39,95 % CI: 0.24 - -0.63)结论:血清DUPAN-2展示了巨大的潜力作为诊断和患者预后的生物标志物的电脑。
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DUPAN-2 in pancreatic cancer: Systematic review and meta-analysis.

Objective: Pancreatic cancer (PC) is a highly aggressive malignancy with poor prognosis and high mortality rate. Identifying reliable biomarkers for the early diagnosis and treatment is urgently needed. This study aims to comprehensively evaluate the diagnostic and prognostic value of DUPAN-2 in PC through a meta-analysis.

Methods: We systematically searched PubMed, Embase, and other databases for studies related to DUPAN-2 and its prognostic and diagnostic relevance in PC, covering publications up to August 2024. We used pooled hazard ratios (HRs) to evaluate the prognostic value of DUPAN-2 in PC, the summary receiver operating characteristic (SROC) curve and the area under the curve (AUC) to assess diagnostic performance, while pooled odds ratios (ORs) analyzed associations with clinicopathological features.

Results: A total of 22 studies involving 4765 patients were included in this meta-analysis, with 11 studies focusing on diagnostic analysis, 10 on prognostic analysis, and 3 on clinicopathological features. The diagnostic meta-analysis revealed a pooled sensitivity of 0.63 (95 % CI: 0.56-0.69), a pooled specificity of 0.98 (95 % CI: 0.95-0.99), and an AUC of 0.83 (95 % CI: 0.79-0.86). Subgroup analysis indicated that a DUPAN-2 threshold at 150 U/mL achieved the highest diagnostic performance. The prognostic meta-analysis demonstrated that elevated DUPAN-2 levels were associated with poorer OS (HR = 1.70, 95 % CI: 1.36-2.14) and PFS (HR = 1.33, 95 % CI: 1.14-1.56). Additionally, the clinicopathological features meta-analysis showed that elevated DUPAN-2 levels were associated with vascular invasion (OR = 3.48, 95 % CI: 1.26-9.59), while normalized DUPAN-2 levels were associated with higher resectability (OR = 0.57, 95 % CI: 0.36-0.90) and lower N-stage (OR = 0.39, 95 % CI: 0.24-0.63) CONCLUSION: Serum DUPAN-2 demonstrates significant potential as a biomarker for diagnosis and prognosis in patients with PC.

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来源期刊
Clinica Chimica Acta
Clinica Chimica Acta 医学-医学实验技术
CiteScore
10.10
自引率
2.00%
发文量
1268
审稿时长
23 days
期刊介绍: The Official Journal of the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) Clinica Chimica Acta is a high-quality journal which publishes original Research Communications in the field of clinical chemistry and laboratory medicine, defined as the diagnostic application of chemistry, biochemistry, immunochemistry, biochemical aspects of hematology, toxicology, and molecular biology to the study of human disease in body fluids and cells. The objective of the journal is to publish novel information leading to a better understanding of biological mechanisms of human diseases, their prevention, diagnosis, and patient management. Reports of an applied clinical character are also welcome. Papers concerned with normal metabolic processes or with constituents of normal cells or body fluids, such as reports of experimental or clinical studies in animals, are only considered when they are clearly and directly relevant to human disease. Evaluation of commercial products have a low priority for publication, unless they are novel or represent a technological breakthrough. Studies dealing with effects of drugs and natural products and studies dealing with the redox status in various diseases are not within the journal''s scope. Development and evaluation of novel analytical methodologies where applicable to diagnostic clinical chemistry and laboratory medicine, including point-of-care testing, and topics on laboratory management and informatics will also be considered. Studies focused on emerging diagnostic technologies and (big) data analysis procedures including digitalization, mobile Health, and artificial Intelligence applied to Laboratory Medicine are also of interest.
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