Kubeczko Marcin, Tudrej Patrycja, Tyszkiewicz Tomasz, Krzywon Aleksandra, Oczko-Wojciechowska MaŁgorzata, JarzĄb MichaŁ
Breast Cancer Center, Maria Sklodowska-Curie National Research Institute of Oncology Gliwice Branch, Gliwice, Upper Silesia 44-102, Poland.
Department of Clinical and Molecular Genetics, Maria Sklodowska-Curie National Research Institute of Oncology Gliwice Branch, Gliwice, Upper Silesia 44-102, Poland.
Oncol Lett. 2024 Feb 28;27(4):181. doi: 10.3892/ol.2024.14314. eCollection 2024 Apr.
Cyclin-dependent kinase 4/6 inhibitors (CDK4/6is) are the mainstay of treatment of hormone receptor/human epidermal growth factor receptor 2-patients with advanced breast cancer (ABC). Despite improvements in overall survival, most patients experience disease progression. Biomarkers derived from a liquid biopsy are appealing for their potential to detect resistance to treatment earlier than computed tomography imaging. However, clinical data concerning microRNAs (miRNAs/miRs) in the context of CDK4/6is are lacking. Thus, the present study assessed the use of miRNAs in patients with ABC treated with CDK4/6is. Patients treated for ABC with CDK4/6is between June and August 2022 were eligible. miRNA expression analyses were performed using a TaqMan low-density miRNA array. A total of 80 consecutive patients with ABC treated with CDK4/6is at Maria Sklodowska-Curie National Research Institute of Oncology (Gliwice, Poland) were assessed, with 14 patients diagnosed with progressive disease at the time of sampling, 55 patients exhibited clinical benefit from CDK4/6i treatment and 11 patients were at the beginning of CDK4/6i treatment. Patients with disease progression had significantly higher levels of miR-21 (P=0.027), miR-34a (P=0.011), miR-193b (P=0.032), miR-200a (P=0.027) and miR-200b (P=0.003) compared with patients who benefitted from CDK4/6i treatment. Significantly higher levels of miR-34a expression were observed in patients with progressive disease than in patients beginning treatment (P=0.031). The present study demonstrated the potential innovative role of circulating miRNAs during CDK4/6i treatment. Plasma-based expression of miR-21, -34a, -193b, -200a and -200b effectively distinguished patients with ABC who responded to CDK4/6i treatment from patients who were resistant. However, longitudinal studies are required to verify the predictive and prognostic potential of miRNA.
细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)是激素受体/人表皮生长因子受体2阴性晚期乳腺癌(ABC)患者治疗的主要手段。尽管总生存期有所改善,但大多数患者仍会出现疾病进展。源自液体活检的生物标志物因其比计算机断层扫描成像更早检测到治疗耐药性的潜力而备受关注。然而,关于CDK4/6i背景下微小RNA(miRNA/miR)的临床数据尚缺乏。因此,本研究评估了miRNA在接受CDK4/6i治疗的ABC患者中的应用。2022年6月至8月期间接受CDK4/6i治疗ABC的患者符合条件。使用TaqMan低密度miRNA阵列进行miRNA表达分析。对波兰格利维采玛丽亚·斯克洛多夫斯卡-居里国家肿瘤研究所连续80例接受CDK4/6i治疗的ABC患者进行了评估,其中14例患者在采样时被诊断为疾病进展,55例患者从CDK4/6i治疗中获得临床获益,11例患者处于CDK4/6i治疗初期。与从CDK4/6i治疗中获益的患者相比,疾病进展患者的miR-21(P=0.027)、miR-34a(P=0.011)、miR-193b(P=0.032)、miR-200a(P=0.027)和miR-200b(P=0.003)水平显著更高。疾病进展患者的miR-34a表达水平明显高于开始治疗的患者(P=0.031)。本研究证明了循环miRNA在CDK4/6i治疗期间的潜在创新作用。基于血浆的miR-21、-34a、-193b、-200a和-200b表达有效地将对CDK4/6i治疗有反应的ABC患者与耐药患者区分开来。然而,需要进行纵向研究来验证miRNA的预测和预后潜力。