Pistelli Mirco, Merloni Filippo, Crocetti Sonia, Scortichini Laura, Tassone Laura, Cantini Luca, Agostinelli Veronica, Bastianelli Lucia, Savini Agnese, Berardi Rossana
Clinica Oncologica e Centro Regionale di Genetica Oncologica, Università Politecnica delle Marche, AOU Ospedali Riuniti, Ancona (AN) 60126, Marche, Italy.
J Oncol. 2021 May 4;2021:5548252. doi: 10.1155/2021/5548252. eCollection 2021.
Systemic neoadjuvant chemotherapy (NCT) is a standard treatment for locally advanced breast cancer (LABC) and for selected early breast cancer (EBC). In these settings, the prognostic and predictive role of Ki-67 before and after NCT is unclear. The aim of our study was to investigate the prognostic role of Ki-67 change in patients not achieving pathological complete response (pCR). We retrospectively analyzed data of patients who did not achieve pCR assessing Ki-67 expression pre- and post-NCT. We stratified three groups: high reduction (>20%), low reduction (1-20%), and no reduction in Ki-67. These groups were correlated with clinical and pathological data by 2 test. We estimated disease-free survival (DFS) and overall survival (OS) using Kaplan-Meier method, and we adopted univariate and multivariate Cox proportional hazard models. We selected 82 patients from a database of 143 patients, excluding those who were metastatic at diagnosis, achieved pCR, or lack data regarding Ki-67. Median age at diagnosis was 54 years (range 30-75); 51 patients were Luminal B, 10 human epidermal growth factor receptor 2 (HER-2) enriched, and 21 triple negative. A significant correlation between high Ki-67 reduction and luminal B HER-2-negative subtype was observed ( = 0,0035). The change in Ki-67 was significantly associated with DFS ( = 0,0596) and OS ( = 0,0120), also at multivariate analysis ( = 0,0256 for DFS; = 0,0093 for OS). In particular, as compared to patients with low/no reduction of Ki-67, those with high Ki-67 reduction (>20%) after NCT showed better survival (60% vs. 56% vs. 83% after 5 years from diagnosis, respectively; = 0.01). In conclusion, in our study, Ki-67 change showed a significant prognostic role in breast cancer patients treated with NCT who did not achieve pCR. Crucially, Ki-67 < 20% identifies a high-risk population that may be eligible for clinical trials with novel therapeutic interventions in adjuvant setting.
全身新辅助化疗(NCT)是局部晚期乳腺癌(LABC)和部分早期乳腺癌(EBC)的标准治疗方法。在这些情况下,NCT前后Ki-67的预后和预测作用尚不清楚。我们研究的目的是调查未达到病理完全缓解(pCR)的患者中Ki-67变化的预后作用。我们回顾性分析了未达到pCR的患者的数据,评估NCT前后的Ki-67表达。我们将患者分为三组:Ki-67高降低组(>20%)、低降低组(1%-20%)和未降低组。通过卡方检验将这些组与临床和病理数据相关联。我们使用Kaplan-Meier方法估计无病生存期(DFS)和总生存期(OS),并采用单变量和多变量Cox比例风险模型。我们从143例患者的数据库中选择了82例患者,排除诊断时已发生转移、达到pCR或缺乏Ki-67数据的患者。诊断时的中位年龄为54岁(范围30-75岁);51例为Luminal B型,10例为富含人表皮生长因子受体2(HER-2)型,21例为三阴性。观察到Ki-67高降低与Luminal B HER-2阴性亚型之间存在显著相关性(P = 0.0035)。Ki-67的变化与DFS(P = 0.0596)和OS(P = 0.0120)显著相关,多变量分析时也是如此(DFS的P = 0.0256;OS的P = 0.0093)。特别是,与Ki-67低降低/未降低的患者相比,NCT后Ki-67高降低(>20%)的患者生存率更高(诊断后5年分别为60%、56%和83%;P = (此处原文有误,推测应为P = 0.01)0.01)。总之,在我们的研究中,Ki-67变化在接受NCT但未达到pCR的乳腺癌患者中显示出显著的预后作用。至关重要地,Ki-67<20%可识别出一个高危人群,该人群可能有资格在辅助治疗中参与新型治疗干预的临床试验。