评价Claudin-4抗原过表达在三阴性乳腺癌患者中的作用:一项5年生存分析。

Q3 Medicine
Iranian Journal of Pathology Pub Date : 2025-01-01 Epub Date: 2025-03-10 DOI:10.30699/ijp.2025.2040168.3350
Maryam Soltan, Azar Naimi, Razieh Hafez Forghan, Marjan Mansourian
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引用次数: 0

摘要

背景与目的:根据分子和病理证据,乳腺癌可分为4组:Luminal A、Luminal B、HER2+肿瘤和三阴性乳腺癌(TNBC)。与其他类型的BC相比,TNBC的生存率较低,复发和转移的机会较高,主要是由于其具有挑战性的治疗过程。Claudin 4 (CLDN4)是细胞间紧密连接中的一种跨膜蛋白,与这些恶性肿瘤的不良预后和更快的疾病进展有关。方法:联系先前诊断为TNBC并检测CLDN4过表达的患者进行随访并确定疾病结局。记录了当前的健康状况、死因和死亡时间(如果适用)。获取患者档案以获取年龄、肿瘤大小和分级、淋巴结累及、转移、Ki67和CLDN4表达等信息。结果:CLDN高表达患者死亡率明显降低。然而,在控制其他协变量后,生存粗模型的风险比(HR)为0.48 (95%CI=[0.13 - 1.27]),经诊断年龄调整后的风险比为0.54 (95%CI=[0.2 - 1.43]),经其他协变量调整后的风险比为0.58 (95%CI=[0.18-1.82])。在粗模型中,CLDN4与肿瘤转移也无相关性(HR=0.64, p=0.203);HR=0.52, p=0.409(经其他协变量调整后)。CLDN4高组患者的肿瘤数量明显高于2cm。结论:虽然已有研究表明CLDN4过表达会恶化TNBC预后,增加转移或复发,但本研究未发现这种关联。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the Role of Claudin-4 Antigen Overexpression in Triple-Negative Breast Cancer Patients: A 5-Year Survival Analysis.

Background & objective: Breast cancer (BC) can be categorized into 4 groups based on molecular and pathological evidence: Luminal A, Luminal B, HER2+ tumors, and triple-negative breast cancer (TNBC). TNBC has a poorer survival rate and a higher chance of recurrence and metastasis compared to other BC types, primarily due to its challenging treatment course. Claudin 4 (CLDN4), a transmembrane protein in tight junctions between cells, has been linked to poor prognosis and faster disease progression in these malignancies.

Methods: Patients previously diagnosed with TNBC and tested for CLDN4 overexpression were contacted for follow-up and to determine disease outcomes. The current health status, cause, and time of death (if applicable) were recorded. Patient files were accessed to obtain information on age, tumor size and grading, lymph node involvement, metastasis, Ki67, and CLDN4 expression.

Results: Patients with high CLDN expression showed a significantly lower mortality rate. However, after controlling for other covariates, the hazard ratio (HR) was 0.48 (95%CI= [0.13 - 1.27]) in the crude model for survival, 0.54 (95%CI = [0.2 - 1.43]) when adjusted for age at diagnosis, and 0.58 (95%CI = [0.18-1.82]) when adjusted for other covariates. CLDN4 was also not correlated with tumor metastasis (HR=0.64, p=0.203, in the crude model; HR=0.52, p=0.409, when adjusted for other covariates). Patients in the CLDN4 high group had a significantly higher number of tumors >2cm.

Conclusion: Although previous studies have shown that CLDN4 overexpression worsens TNBC prognosis and increases metastasis or recurrence, the current study found no such association.

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来源期刊
Iranian Journal of Pathology
Iranian Journal of Pathology Medicine-Pathology and Forensic Medicine
CiteScore
2.00
自引率
0.00%
发文量
99
审稿时长
20 weeks
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