Clinicopathologic and prognostic significance of tumor-associated macrophages in cervical cancer: a systematic review and meta-analysis.

IF 2.8 3区 医学 Q2 ONCOLOGY Clinical & Translational Oncology Pub Date : 2025-01-01 Epub Date: 2024-07-08 DOI:10.1007/s12094-024-03587-1
Xinmei Lin, Jijie Zhan, Ziting Guan, Jingwei Zhang, Tian Li, Li Zhong, Changlin Zhang, Miao Li
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Abstract

Objectives: The role of tumor-associated macrophages (TAMs) in cervical cancer (CC) remains controversial. Here, we report a meta-analysis of the association between TAMs infiltration and clinical outcomes.

Methods: PubMed, Embase, Web of Science, and CNKI were searched systematically from inception until December 20, 2023. Studies involving TAMs and prognosis, clinical, or pathological features were included. Quality assessments of the selected studies were assessed. The fixed-effect or random-effects model, standard mean difference (SMD), odds ratios (OR), or hazard ratios (HR) with 95% confidence intervals (CIs) were used as the effect size estimate.

Results: 26 eligible studies with 2,295 patients were identified. Our meta-analysis revealed that TAMs were overexpressed in CC (OR = 12.93, 95% CI = 7.73-21.61 and SMD = 1.58, 95% CI = 0.95-2.21) and that elevated TAM levels were strongly associated with lymph node metastasis (LNM) (SMD = 0.51, 95% CI = 0.90-2.01) and FIGO stages (SMD = 0.46, 95% CI = 0.08-0.85). Subgroup analysis indicated a significant positive correlation between LNM and TAMs density in tumor stroma, but not in cancer nests (SMD = 0.58, 95% CI = 0.31-0.58). Furthermore, in early stage, a stronger correlation exists between LNM and TAM density (SMD = 1.21, 95% CI = 0.75-1.66). In addition, it revealed that patients with high TAMs expression had poorer overall survival (OS) (HR = 2.55 95% CI = 1.59-4.07) and recurrence-free survival (RFS) (HR = 2.17, 95% CI = 1.40-3.35).

Conclusions: Our analyses suggest that a high density of TAMs predicts adverse outcomes in CC.

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宫颈癌中肿瘤相关巨噬细胞的临床病理和预后意义:系统综述和荟萃分析。
目的:肿瘤相关巨噬细胞(TAMs)在宫颈癌(CC)中的作用仍存在争议。在此,我们报告了一项关于 TAMs 浸润与临床结果之间关系的荟萃分析:方法:对 PubMed、Embase、Web of Science 和 CNKI 进行了系统检索。纳入了涉及 TAMs 和预后、临床或病理特征的研究。对所选研究进行了质量评估。采用固定效应或随机效应模型、标准平均差(SMD)、几率比(OR)或带95%置信区间(CI)的危险比(HR)来估计效应大小。我们的荟萃分析显示,TAMs在CC中过表达(OR = 12.93,95% CI = 7.73-21.61,SMD = 1.58,95% CI = 0.95-2.21),TAM水平升高与淋巴结转移(LNM)(SMD = 0.51,95% CI = 0.90-2.01)和FIGO分期(SMD = 0.46,95% CI = 0.08-0.85)密切相关。亚组分析表明,LNM 与肿瘤基质中的 TAMs 密度呈显著正相关,但与癌巢中的 TAMs 密度无关(SMD = 0.58,95% CI = 0.31-0.58)。此外,在早期阶段,LNM 和 TAM 密度之间存在更强的相关性(SMD = 1.21,95% CI = 0.75-1.66)。此外,研究还发现,TAMs高表达的患者总生存期(OS)(HR = 2.55 95% CI = 1.59-4.07)和无复发生存期(RFS)(HR = 2.17, 95% CI = 1.40-3.35)较差:我们的分析表明,TAMs的高密度可预测CC的不良预后。
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来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
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