Jung Youn Joo, Lee Seungju, Kang Seok Kyeong, Kim Jee Yeon, Choo Ki Seok, Nam Kyung Jin, Joo Ji Hyeon, Kim Jae Joon, Kim Hyun Yul
Department of Surgery, Research Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Republic of Korea.
Department of Pathology, Pusan National University Yangsan Hospital, Pusan National University School of Medicine, Yangsan, Republic of Korea.
Oncology. 2025;103(5):351-359. doi: 10.1159/000541019. Epub 2024 Sep 9.
Human epidermal growth factor receptor 2 (HER2)-targeted therapies have shown effectiveness against HER2-positive breast cancer. This makes neoadjuvant chemotherapy (NAC) a valuable option for treating both early and advanced stages of the disease. The tumor's response to HER2-targeted NAC provides crucial prognostic information. Additionally, it allows for tailoring adjuvant treatment strategies for HER2+ breast cancer based on pathological responses. This study aimed to investigate the clinicopathological factors that influence tumor response.
We retrospectively analyzed 122 patients diagnosed with HER2+ breast cancer. These patients received NAC and HER2-directed therapy between January 2018 and December 2022 at the Pusan National University Yangsan Hospital. Following surgery, tumor response was evaluated, categorizing patients into two groups: pathological complete response (pCR) and non-pCR groups. We analyzed data on various factors, including age, NAC regimen, type of breast and axillary surgery, clinical stage (cTNM), historical grade, and preoperative levels of carcinoembryonic antigen, cancer antigen 15-3 (CA 15-3), estrogen receptor (ER), progesterone receptor (PR), HER2, p53, and KI-67.
Out of the 122 patients, 75 achieved pCR, while 47 did not. Most clinicopathological factors showed no significant difference between the pCR and non-pCR groups. However, several factors were associated with a higher pCR rate: normal preoperative CA 15-3 levels (odds ratio [OR]: 3.74, confidence interval [CI]: 1.19-11.72, p = 0.02), preoperative ER positivity (OR: 2.65, CI: 1.25-5.59, p = 0.01), PR negativity (OR: 3.92, CI: 1.82-8.45, p < 0.05), and strong preoperative HER2 immunohistochemistry (IHC) 3+ staining. Multivariate analysis confirmed that PR negativity (OR: 2.8, CI: 1.23-6.42, p = 0.01) and strong preoperative HER2 IHC 3+ staining (OR: 0.18, CI: 0.03-0.84, p = 0.04) were independent predictors of a higher pCR rate.
A pCR after NAC impacts patient prognosis and influences the choice of adjuvant treatment for HER2+ breast cancer. Clinicopathological factors can help predict responses to HER2-targeted NAC. In our study, pre-ER/PR negativity, high pre-HER2 levels, and normal CA 15-3 levels were found to be potential predictors of pCR. These findings may contribute to developing more effective treatment strategies for HER2+ breast cancer.
人表皮生长因子受体2(HER2)靶向治疗已显示出对HER2阳性乳腺癌的有效性。这使得新辅助化疗(NAC)成为治疗该疾病早期和晚期的一个有价值的选择。肿瘤对HER2靶向NAC的反应提供了关键的预后信息。此外,它还允许根据病理反应为HER2 +乳腺癌量身定制辅助治疗策略。本研究旨在调查影响肿瘤反应的临床病理因素。
我们回顾性分析了122例诊断为HER2 +乳腺癌的患者。这些患者于2018年1月至2022年12月在釜山国立大学梁山医院接受了NAC和HER2导向治疗。手术后,评估肿瘤反应,将患者分为两组:病理完全缓解(pCR)组和非pCR组。我们分析了各种因素的数据,包括年龄、NAC方案、乳房和腋窝手术类型、临床分期(cTNM)、组织学分级以及术前癌胚抗原、癌抗原15-3(CA 15-3)、雌激素受体(ER)、孕激素受体(PR)、HER2、p53和KI-67水平。
122例患者中,75例达到pCR,47例未达到。大多数临床病理因素在pCR组和非pCR组之间无显著差异。然而,有几个因素与较高的pCR率相关:术前CA 15-3水平正常(比值比[OR]:3.74,置信区间[CI]:1.19-11.72,p = 0.02)、术前ER阳性(OR:2.65,CI:1.25-5.59,p = 0.01)、PR阴性(OR:3.92,CI:1.82-8.45,p < 0.05)以及术前HER2免疫组化(IHC)3+强染色。多因素分析证实,PR阴性(OR:2.8,CI:1.23-6.42,p = 0.01)和术前HER2 IHC 3+强染色(OR:0.18,CI:0.03-0.84,p = 0.04)是较高pCR率的独立预测因素。
NAC后的pCR影响患者预后并影响HER2 +乳腺癌辅助治疗的选择。临床病理因素有助于预测对HER2靶向NAC的反应。在我们的研究中,术前ER/PR阴性、术前HER2水平高和CA 15-3水平正常被发现是pCR的潜在预测因素。这些发现可能有助于为HER2 +乳腺癌制定更有效的治疗策略。