Department of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Hacettepe University, Ankara, Turkey.
Department of Internal Medicine, Division of Medical Oncology, Faculty of Medicine, Dr. Abdurrahman Yurtaslan Ankara Oncology Research and Education Hospital, Ankara, Turkey.
Medicine (Baltimore). 2024 Jul 26;103(30):e38828. doi: 10.1097/MD.0000000000038828.
The fact that the human epidermal growth factor receptor 2 (HER2)-low group, historically classified as HER2 negative in breast cancer histology, benefited from HER2-targeted treatments similarly to the HER2-positive group indicates that this group has a distinct histology from the HER2-0 group. The effectiveness of cyclin-dependent kinase 4/6 inhibitors, which are the standard first-line treatment for hormone receptor-positive, HER2-negative advanced breast cancer, in this newly defined histological subgroup remains a topic of debate. In our study, we examined the impact of HER2 status on the efficacy of CDK4/6 inhibitors. Our study is a retrospective, multicenter, real-world data analysis. One hundred sixty patients were included in the study. The relationship between HER2 status and other clinical-pathological features, as well as progression-free survival, was examined. Median follow-up was 20.33 ± 0.98 months. The mPFS could not be reached. All patients exhibited positive estrogen receptor expression. Among the patients, 111 (69.4%) were categorized as HER2-0, and 49 (30.6%) as HER2-low. The 24-month progression-free survival rates were similar between HER2-0 and HER2-low patients (60.6% vs 65.3%, hormone receptor: 1.18, CI: 0.67-2.20, P = .554). We established that the mPFS achieved with cyclin-dependent kinase 4/6 inhibitors as a first-line therapy for patients with advanced breast cancer is unaffected by HER2 status.
人表皮生长因子受体 2(HER2)低组,在乳腺癌组织学中既往被归类为 HER2 阴性,但其从 HER2 靶向治疗中获益与 HER2 阳性组相似,这表明该组与 HER2-0 组具有不同的组织学特征。在新定义的组织学亚组中,细胞周期蛋白依赖性激酶 4/6 抑制剂(CDK4/6 抑制剂)的有效性,即激素受体阳性、HER2 阴性晚期乳腺癌的标准一线治疗,仍然是一个有争议的话题。在我们的研究中,我们研究了 HER2 状态对 CDK4/6 抑制剂疗效的影响。我们的研究是一项回顾性、多中心、真实世界数据分析。研究纳入了 160 例患者。我们考察了 HER2 状态与其他临床病理特征以及无进展生存期之间的关系。中位随访时间为 20.33±0.98 个月。无进展生存期(mPFS)无法达到。所有患者均表现出雌激素受体阳性。其中,111 例(69.4%)患者为 HER2-0,49 例(30.6%)为 HER2 低表达。HER2-0 与 HER2 低表达患者的 24 个月无进展生存率相似(60.6% vs 65.3%,激素受体:1.18,CI:0.67-2.20,P=0.554)。我们的研究确立了 CDK4/6 抑制剂作为晚期乳腺癌一线治疗药物,其 mPFS 不受 HER2 状态的影响。