← 返回

三阴性乳腺癌中雄激素受体表达与 TIL(肿瘤浸润淋巴细胞)的临床病理学意义:一项回顾性队列研究

英文原题:Clinicopathological significance of androgen receptor expression and tumor infiltrating lymphocytes in triple-negative breast cancer: a retrospective cohort study.

查看英文原题

Clinicopathological significance of androgen receptor expression and tumor infiltrating lymphocytes in triple-negative breast cancer: a retrospective cohort study.

PubMed 2024/12/27(内容时间) Breast Cancer Q1 · IF 3.7(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

利用治疗前活检进行的 AR/TIL 分类识别出具有不同 NAC 反应和预后的 TNBC 亚组。

中文摘要

三阴性乳腺癌(TNBC)是一种治疗选择有限的严重疾病。本研究探讨雄激素受体(AR)表达和TIL(肿瘤浸润淋巴细胞)在预测TNBC新辅助化疗(NAC)耐药中的意义。研究假设,利用治疗前活检进行AR/TIL分类可识别NAC耐药亚群,并加深对大汗腺样分化的认识。

本项回顾性研究纳入156名连续接受NAC治疗的TNBC患者。若肿瘤细胞核染色比例≥1%,则定义为AR免疫染色阳性。评估间质TIL水平,并将≥50%定义为高水平。采用抗15-PGDH抗体检测大汗腺样分化,并评估NAC后的病理学应答。

总体而言,36%(n=56)的患者达到病理完全缓解(pCR)。AR阳性/TIL低水平肿瘤未达到pCR的比例较高(76%,42/55),表现为NAC耐药。Kaplan-Meier曲线显示,4个AR/TIL亚组的总生存期(OS)和无远处转移生存期(DMFS)存在显著差异(OS:p=0.013;DMFS:p=0.0016)。所有11例存在一定程度大汗腺样分化的病例均为AR阳性/TIL低水平、15-PGDH阳性且对NAC耐药。AR阳性/TIL低水平状态与未达到pCR的较高可能性显著相关(OR=0.26,p=0.009)。多变量分析确认,pCR是预后较好的独立预测因素(OS:HR=0.13,p=0.006;DMFS:HR=0.15,p=0.002);而AR阳性/TIL低水平状态与OS或DMFS无显著相关。

基于治疗前活检的AR/TIL分类可识别具有不同NAC应答和预后的TNBC亚组。包括大汗腺样分化病例在内的AR阳性/TIL低水平TNBC对NAC耐药,提示需要替代疗法。

展开英文摘要原文

Triple-negative breast cancer (TNBC) is a serious disease with limited treatment options. We explored the significance of androgen receptor (AR) expression and tumor-infiltrating lymphocytes (TILs) in predicting neoadjuvant chemotherapy (NAC) resistance in TNBC, hypothesizing that AR/TIL classification using pretreatment biopsies can identify NAC-resistant subgroups and improve the understanding of apocrine differentiation.

This retrospective study included 156 consecutive patients with TNBC treated with NAC. AR immunostaining was defined positive if 1% of the tumor cell nuclei were stained. Stromal TIL levels were assessed, with high levels defined as 50%. Apocrine differentiation was detected using an anti-15-PGDH antibody. The pathological response to NAC was evaluated.

Overall, 36% (n = 56) of the patients achieved a pathological complete response (pCR). AR + /TIL low tumors had a high non-pCR rate (76%, 42/55) and were resistant to NAC. Kaplan-Meier plots showed significant differences in overall survival (OS) and distant metastasis-free survival (DMFS) among the four AR/TIL subgroups (OS: p = 0.013; DMFS: p = 0.0016). All 11 cases with some degree of apocrine differentiation were AR + /TIL low , 15-PGDH-positive, and NAC-resistant. AR + /TIL low status was significantly associated with a high likelihood of non-pCR (OR = 0.26, p = 0.009). Multivariate analysis confirmed pCR as an independent predictor of better prognosis (OS, HR = 0.13, p = 0.006; DMFS, HR = 0.15, p = 0.002), whereas AR + /TIL low status was not significantly associated with OS or DMFS.

AR/TIL classification using pretreatment biopsies identified TNBC subgroups with distinct NAC responses and prognoses. AR + /TIL low TNBC, including apocrine differentiation cases, were NAC-resistant, highlighting the need for alternative therapies.

论文信息

作者
Ushigusa T、Hirakawa N、Kajiura Y、Yoshida A、Yamauchi H、Kanomata N
单位
Department of Pathology, St. Luke's International Hospital, 9-1, Akashi-cho, Chuo-ku, Tokyo, 1048560, Japan. taushig@luke.ac.jp.Japan
期刊
Breast cancer (Tokyo, Japan)2025 Mar
原文标识
PubMed 39729292 · DOI 10.1007/s12282-024-01662-7