评估乳腺癌患者肿瘤大小、淋巴结状态和ER/PR/HER2表达的关系

IF 0.8 4区 医学 Q4 IMMUNOLOGY
Liqin Wu, Xianghua Zhou, Fanfan Yang
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引用次数: 0

摘要

本研究旨在探讨乳腺癌患者肿瘤大小、淋巴结状态与ER/PR/HER2表达的关系。选取在我院接受手术治疗的117例乳腺癌患者作为研究对象。所有患者术中均行同侧腋窝淋巴结清扫或前哨淋巴结活检。收集原发病变的病理资料及超声特征。通过单因素和多因素logistic回归分析,评价肿瘤大小、淋巴结状态与ER/PR/HER2表达的关系,并探讨乳腺癌患者淋巴结转移的危险因素。117例患者中同侧腋窝淋巴结转移阳性48例,阴性69例。单因素分析显示,年龄、PR状态、分子亚型与淋巴结转移无显著相关性(P < 0.05)。单因素分析显示,肿瘤大小、病理类型、绝经状态、Ki67表达、HER2状态、ER状态与淋巴结转移有显著相关性(P < 0.05)。Logistic回归进一步确定肿瘤大小[优势比(OR) = 1.809, 95%可信区间(CI): 1.075 ~ 3.428, P = 0.018]、病理类型(OR = 2.947, 95% CI: 1.247 ~ 7.536, P = 0.012)、Ki67表达(OR = 15.923, 95% CI: 3.219 ~ 74.512, P = 0.001)、HER2状态(OR = 2.509, 95% CI: 1.586 ~ 5.769, P = 0.015)、ER状态(OR = 3.226, 95% CI: 1.408 ~ 8.277, P = 0.007)为淋巴结转移的独立危险因素。本研究发现,乳腺癌患者的淋巴结转移与肿瘤较大(> 20 mm)、浸润性肿瘤类型、Ki67高表达、HER2阳性、ER阴性相关。这些发现强调了将这些风险因素纳入临床评估以指导个体化治疗计划的重要性。通过识别淋巴结转移风险升高的患者,临床医生可以更好地定制治疗策略,以改善患者的预后并优化治疗干预措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing the Relationship among Tumor Size, Lymph Node Status, and ER/PR/HER2 Expression in Patients with Breast Cancer.

This study aims to explore the relationship between tumor size, lymph node status, and ER/PR/HER2 expression in breast cancer patients. A total of 117 breast cancer patients who underwent surgery at our hospital were selected as the research objects. All patients underwent ipsilateral axillary lymph node dissection or sentinel lymph node biopsy during surgery. Pathological data and ultrasound features of primary lesions were collected. Univariate and multivariate logistic regression analyses were performed to evaluate the relationship between tumor size, lymph node status, and ER/PR/HER2 expression, as well as to identify the risk factors for lymph node metastasis in breast cancer patients. Among the 117 patients, 48 were positive for ipsilateral axillary lymph node metastasis and 69 were negative. Univariate analysis showed no significant correlation between age, PR status, molecular subtype, and lymph node metastasis (P > 0.05). Univariate analysis showed that tumor size, pathological type, menopausal status, Ki67 expression, HER2 status, and ER status were significantly associated with lymph node metastasis (P < 0.05). Logistic regression further identified tumor size [odds ratio (OR) = 1.809, 95% confidence interval (CI): 1.075-3.428, P = 0.018), pathological type (OR = 2.947, 95% CI: 1.241-7.536, P = 0.012), Ki67 expression (OR = 15.923, 95% CI: 3.219-74.512, P = 0.001), HER2 status (OR = 2.509, 95% CI: 1.586-5.769, P = 0.015), and ER status (OR = 3.226, 95% CI: 1.408-8.277, P = 0.007) as independent risk factors for lymph node metastasis. This study reveals that lymph node metastasis in breast cancer patients is significantly associated with larger tumor size (> 20 mm), invasive tumor type, higher Ki67 expression, HER2 positivity, and ER negativity. These findings emphasize the importance of incorporating these risk factors into clinical assessments to guide individualized treatment planning. By identifying patients with elevated lymph node metastasis risk, clinicians can better tailor treatment strategies to improve patient outcomes and optimize therapeutic interventions.

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来源期刊
CiteScore
2.60
自引率
0.00%
发文量
14
审稿时长
>12 weeks
期刊介绍: Immunology covers a broad spectrum of investigations at the genes, molecular, cellular, organ and system levels to reveal defense mechanisms against pathogens as well as protection against tumors and autoimmune diseases. The great advances in immunology in recent years make this field one of the most dynamic and rapidly growing in medical sciences. Critical ReviewsTM in Immunology (CRI) seeks to present a balanced overview of contemporary adaptive and innate immune responses related to autoimmunity, tumor, microbe, transplantation, neuroimmunology, immune regulation and immunotherapy from basic to translational aspects in health and disease. The articles that appear in CRI are mostly obtained by invitations to active investigators. But the journal will also consider proposals from the scientific community. Interested investigators should send their inquiries to the editor before submitting a manuscript.
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