Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea; Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea; Translational Medicine, Seoul National University College of Medicine, Seoul, Korea.
Department of Pathology, Seoul National University Hospital, Seoul, Korea.
Eur J Cancer. 2024 Dec;213:115081. doi: 10.1016/j.ejca.2024.115081. Epub 2024 Oct 20.
There is a strong rationale for targeting HER3, as HER3 contributes to tumorigenesis and treatment resistance. However, the prognostic role of HER3 and their association with immunoregulatory protein expression has not been established.
The main objective of this study was to investigate the prognostic role of HER3 expression and identify immunoregulatory marker expression according to HER3 status. HER3 expression and 10 immunoregulatory protein (PD-1/PD-L1/PD-L2/IDO/TIM-3/OX40/OX40L/B7-H2/B7-H3/B7-H4) expression was identified in 320 stage I-III breast cancer patients who received curative surgery at Seoul National University Hospital in 2008. The median follow-up duration was 88.8 months. Criteria for HER3 IHC was adopted from HER2 IHC score and only those with 3 + was considered positive.
Among 320 patients, 213 (67.2 %) had luminal A disease, 30 (9.5 %) had luminal B disease, 28 (8.8 %) had HER2-positive disease, and 46 (14.5 %) had triple negative disease. HER3 expression was shown in 153 patients (47.8 %). Tumors with HER3-expression had more immunogenic tumor microenvironment compared to HER3-negative tumor. In addition, patients with HER3 expression had favorable 5-year relapse free survival compared to HER3-negative patients (5-year RFS 92.5 % vs. 85.2 %, p = 0.038). However, in the multivariate analysis, HER3 expression was not a prognostic factor, but expression of immunoregulatory protein was a prognostic factor.
This study identified immunoregulatory protein expression according to HER3 status in breast cancer patients. As tumor with HER3 expression have more immunogenic microenvironment, investigating combination treatment of HER3 targeting agent and immunotherapy in HER3 expressing breast cancer may be promising.
针对 HER3 进行靶向治疗具有很强的理论依据,因为 HER3 有助于肿瘤发生和治疗耐药。然而,HER3 的预后作用及其与免疫调节蛋白表达的关系尚未确定。
本研究的主要目的是探讨 HER3 表达的预后作用,并根据 HER3 状态确定免疫调节标志物的表达。在 2008 年于首尔国立大学医院接受根治性手术的 320 例 I-III 期乳腺癌患者中,检测了 HER3 表达和 10 种免疫调节蛋白(PD-1/PD-L1/PD-L2/IDO/TIM-3/OX40/OX40L/B7-H2/B7-H3/B7-H4)的表达。中位随访时间为 88.8 个月。HER3 的 IHC 标准采用 HER2 IHC 评分,仅将 3+视为阳性。
在 320 例患者中,213 例(67.2%)为 luminal A 型疾病,30 例(9.5%)为 luminal B 型疾病,28 例(8.8%)为 HER2 阳性疾病,46 例(14.5%)为三阴性疾病。153 例(47.8%)患者 HER3 表达阳性。与 HER3 阴性肿瘤相比,HER3 表达阳性肿瘤具有更具免疫原性的肿瘤微环境。此外,与 HER3 阴性患者相比,HER3 表达患者具有更有利的 5 年无复发生存率(5 年 RFS 92.5%对 85.2%,p=0.038)。然而,在多因素分析中,HER3 表达不是预后因素,但免疫调节蛋白的表达是预后因素。
本研究在乳腺癌患者中根据 HER3 状态确定了免疫调节蛋白的表达。由于 HER3 表达的肿瘤具有更具免疫原性的微环境,因此在 HER3 表达的乳腺癌中研究 HER3 靶向药物与免疫疗法的联合治疗可能具有前景。