Douganiotis George, Kesisis George, Lalla Efthalia, Korantzis Ippokratis, Boukovinas Ioannis, Papazisis Konstantinos
3rd Department of Medical Oncology, Theageneion Cancer Hospital, Thessaloniki, Greece.
Oncology Department, Saint Luke Private Hospital, Thessaloniki, Greece.
Cancer Diagn Progn. 2022 Sep 3;2(5):585-591. doi: 10.21873/cdp.10146. eCollection 2022 Sep-Oct.
BACKGROUND/AIM: Low expression of HER2 has defined a new "HER2-low" subgroup of breast cancer with distinct clinicopathological characteristics and both prognostic and predictive implications. The impact of low HER2 expression in metastatic hormone receptor-positive HER2-negative breast cancer treated with first-line CDK4/6 inhibitors has not been studied. Using real-world patient data, we aimed to identify prognostic differences in this patient population according to HER2 expression with immunohistochemistry.
We retrospectively analyzed 191 patients from 5 Oncology Department databases in Thessaloniki, Greece, with hormone receptor-positive HER2-negative metastatic breast cancer treated with CDK4/6 inhibitors in the first line, for whom detailed immunohistochemical HER2 data could be retrieved.
Median progression-free survival was numerically different among the different HER2 subgroups (3.35 years for HER2 0 tumors, 2.18 years for HER2 +1 tumors, 1.74 years for HER2 +2/ISH-negative tumors), but this difference was not statistically significant (p=0.477). Median PFS was statistically significantly longer in patients without visceral metastases (5.45 years) compared to patients with visceral metastases (1.61 years) (p=0.017). Median PFS was also statistically significantly longer in patients taking an aromatase inhibitor (2.99 years) compared to patients taking fulvestrant (1.33 years) (p<0.0001). There were no statistically significant differences in the other subgroups examined.
CDK4/6 inhibitors are equally effective as first-line treatment agents, regardless of the exact level of HER2 expression. Numerical differences, however, do exist among the different HER2 subgroups, and merit further evaluation in future studies to better study this phenomenon.
背景/目的:HER2低表达定义了一种新的乳腺癌“HER2低表达”亚组,具有独特的临床病理特征以及预后和预测意义。一线使用CDK4/6抑制剂治疗的转移性激素受体阳性HER2阴性乳腺癌中,HER2低表达的影响尚未得到研究。我们利用真实世界的患者数据,旨在根据免疫组化检测的HER2表达情况,确定该患者群体的预后差异。
我们回顾性分析了来自希腊塞萨洛尼基5个肿瘤科数据库的191例患者,这些患者均为一线接受CDK4/6抑制剂治疗的激素受体阳性HER2阴性转移性乳腺癌患者,且能获取详细的HER2免疫组化数据。
不同HER2亚组的无进展生存期(PFS)中位数在数值上有所不同(HER2 0肿瘤为3.35年,HER2 +1肿瘤为2.18年,HER2 +2/ISH阴性肿瘤为1.74年),但这种差异无统计学意义(p = 0.477)。与有内脏转移的患者(1.61年)相比,无内脏转移的患者PFS中位数在统计学上显著更长(5.45年)(p = 0.017)。与接受氟维司群治疗的患者(1.33年)相比,接受芳香化酶抑制剂治疗的患者PFS中位数在统计学上也显著更长(2.99年)(p<0.0001)。在所检查的其他亚组中无统计学显著差异。
无论HER2表达的确切水平如何,CDK4/6抑制剂作为一线治疗药物同样有效。然而,不同HER2亚组之间确实存在数值差异,值得在未来研究中进一步评估,以更好地研究这一现象。