Cabioglu Neslihan, Onder Semen, Karatay Hüseyin, Bayram Aysel, Oner Gizem, Tukenmez Mustafa, Muslumanoglu Mahmut, Igci Abdullah, Dinccag Ahmet, Ozmen Vahit, Aydiner Adnan, Saip Pınar, Yavuz Ekrem
Department of General Surgery, Istanbul Faculty of Medicine, Istanbul University, Istanbul 34452, Turkey.
Department of Pathology, Istanbul Faculty of Medicine, Istanbul University, Istanbul 34452, Turkey.
Cancers (Basel). 2024 Jun 28;16(13):2388. doi: 10.3390/cancers16132388.
We aim to investigate any possible associations between chemokine receptor expression and responses to neoadjuvant chemotherapy (NAC) along with outcomes in patients with triple-negative breast cancer (TNBC) with locally advanced disease.
Expressions of chemokine receptors were examined immunohistochemically after staining archival tissue of surgical specimens (n = 63) using specific antibodies for CCR5, CCR7, CXCR4, and CXCR5.
Patients with high CCR5, CCR7, CXCR4, and CXCR5 expression on tumors and high CXCR4 expression on tumor-infiltrating lymphocytes (TILs) were less likely to have a pathological complete response (pCR) or Class 0-I RCB-Index compared to others. Patients with residual lymph node metastases (ypN-positive), high CCR5, and high CXCR4 expressions had an increased hazard ratio (HR) compared to others (DFS: HR = 2.655 [1.029-6.852]; DSS: HR = 2.763 [1.008-7.574]), (DFS: HR = 2.036 [0.805-5.148]; DSS: HR = 2.689 [1.020-7.090]), and (DFS: HR = 2.908 [1.080-7.829]; DSS: HR = 2.132 (0.778-5.846)), respectively. However, patients without CXCR5 expression had an increased HR compared to those with CXCR5 (DFS: 2.838 [1.266-6.362]; DSS: 4.211 [1.770-10.016]).
High expression of CXCR4 and CCR5 was found to be associated with poor prognosis, and CXCR5 was associated with poor chemotherapy response in the present cohort with locally advanced TNBC. Our results suggest that patients with TNBC could benefit from a chemokine receptor inhibitor therapy containing neoadjuvant chemotherapy protocols.
我们旨在研究趋化因子受体表达与新辅助化疗(NAC)反应之间的任何可能关联,以及局部晚期三阴性乳腺癌(TNBC)患者的预后情况。
使用针对CCR5、CCR7、CXCR4和CXCR5的特异性抗体,对手术标本(n = 63)的存档组织进行免疫组化染色,检测趋化因子受体的表达。
与其他患者相比,肿瘤上CCR5、CCR7、CXCR4和CXCR5高表达以及肿瘤浸润淋巴细胞(TILs)上CXCR4高表达的患者不太可能出现病理完全缓解(pCR)或0-I级RCB指数。与其他患者相比,有残留淋巴结转移(ypN阳性)、CCR5高表达和CXCR4高表达的患者的风险比(HR)增加(无病生存期:HR = 2.655 [1.029 - 6.852];疾病特异性生存期:HR = 2.763 [1.008 - 7.574]),(无病生存期:HR = 2.036 [0.805 - 5.148];疾病特异性生存期:HR = 2.689 [1.020 - 7.090]),以及(无病生存期:HR = 2.908 [1.080 - 7.829];疾病特异性生存期:HR = 2.132 [0.778 - 5.846])。然而,与有CXCR5表达的患者相比,无CXCR5表达的患者的HR增加(无病生存期:2.838 [1.266 - 6.362];疾病特异性生存期:4.211 [1.770 - 10.016])。
在本局部晚期TNBC队列中,发现CXCR4和CCR5高表达与预后不良相关,而CXCR5与化疗反应不良相关。我们的结果表明,TNBC患者可能从包含新辅助化疗方案的趋化因子受体抑制剂治疗中获益。