Survival and Clinicopathological Significance of CD47 in Human Solid Tumors: An Updated Systematic Reviews and Meta-Analysis

IF 1.9 Q4 ONCOLOGY
Cancer reports Pub Date : 2025-08-05 DOI:10.1002/cnr2.70296
Yongzhi Ye, Meiqiong Chen, Fada Ji, Suicai Mi, Zhixiong Chen, Xiaowei Wu, Qiurong He, Xiaodong Liu
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Abstract

Background

High expression levels of cluster of differentiation 47 (CD47) have been recognized as poor survival in several different cancers. Nevertheless, the significance of CD47 in patients with solid tumors remains controversial.

Aims

The objective of this study is to elucidate whether elevated CD47 expression independently predicts a poor prognosis across solid tumors through pooled survival and clinicopathological analyses.

Methods and Results

This meta-analysis was based on a search of PubMed, Embase, and Web of Science databases to obtain 20 eligible published studies (totaling 4019 patients) between January 2018 and January 2024. The combined hazard ratios (HRs) for overall survival (OS) were evaluated, and the HRs for relapse-free survival (RFS), progression-free survival (PFS), and disease-free survival (DFS), as well as odds ratios for clinicopathological data, were also respectively combined. The data obtained from these studies were extracted from these published studies and analyzed. This study suggested that CD47 overexpression was related to shorter OS times in human solid tumors, with a combined HR for OS (according to the univariate analysis) of HR = 1.63 (95% confidence intervals,[ 95% CIs]: 1.45–1.83; p < 0.00001), and a pooled HR for OS (according to the multivariate analysis) of HR = 2.02 (95% CI: 1.43–2.84; p < 0.0001). The subgroup analysis revealed that CD47 overexpression was related to inferior OS rates according to country, cancer type, sample size, analysis type, and the method via which the HR value was obtained (i.e., reported or extracted; p < 0.05); in addition, a high expression level of CD47 was also a predictor of poor DFS, PFS, and RFS rates (p < 0.00001). Certain factors, such as age (≥ 60 years old), lymph node metastasis, TNM staging, differentiation type, and tumor recurrence, resulted in an upregulation of CD47 (p < 0.05).

Conclusion

This meta-analysis indicates that CD47 overexpression is significantly associated with poor clinical outcomes, advanced clinical stages, and poor differentiation in solid tumor patients, particularly, in cases involving tumors in the digestive and respiratory systems. These findings suggest that CD47 could serve as a valuable prognostic biomarker and therapeutic target.

Abstract Image

CD47在人类实体肿瘤中的生存和临床病理意义:最新的系统综述和荟萃分析
在多种不同的癌症中,CD47的高表达水平被认为是低生存率的原因。然而,CD47在实体瘤患者中的意义仍然存在争议。本研究的目的是通过汇总生存和临床病理分析阐明CD47表达升高是否独立预测实体瘤的不良预后。方法和结果本荟萃分析基于对PubMed、Embase和Web of Science数据库的搜索,以获得2018年1月至2024年1月期间20项符合条件的已发表研究(共4019例患者)。评估总生存期(OS)的联合风险比(HRs),并分别合并无复发生存期(RFS)、无进展生存期(PFS)和无病生存期(DFS)的联合风险比以及临床病理资料的优势比。从这些研究中获得的数据是从这些已发表的研究中提取并分析的。本研究表明,CD47过表达与人类实体肿瘤中较短的OS时间有关,OS的综合HR(根据单变量分析)为HR = 1.63(95%置信区间,[95% ci]: 1.45-1.83;p < 0.00001), OS的合并HR(根据多变量分析)= 2.02 (95% CI: 1.43-2.84;p < 0.0001)。亚组分析显示,根据国家、癌症类型、样本量、分析类型和获得HR值的方法(即报告或提取;p < 0.05);此外,CD47的高表达水平也是低DFS、PFS和RFS率的预测因子(p < 0.00001)。年龄(≥60岁)、淋巴结转移、TNM分期、分化类型、肿瘤复发等因素可导致CD47表达上调(p < 0.05)。结论本荟萃分析表明,CD47过表达与实体瘤患者的不良临床结局、晚期临床分期和差分化显著相关,特别是在涉及消化和呼吸系统的肿瘤中。这些发现表明CD47可以作为一种有价值的预后生物标志物和治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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