McCartney Amelia, Migliaccio Ilenia, Bonechi Martina, Biagioni Chiara, Romagnoli Dario, De Luca Francesca, Galardi Francesca, Risi Emanuela, De Santo Irene, Benelli Matteo, Malorni Luca, Di Leo Angelo
"Sandro Pitigliani" Department of Medical Oncology, Hospital of Prato, Prato, Italy.
"Sandro Pitigliani" Translational Research Unit, Hospital of Prato, Prato, Italy.
Front Oncol. 2019 Jul 23;9:666. doi: 10.3389/fonc.2019.00666. eCollection 2019.
The recent arrival of CDK4/6 inhibitor agents, with an approximate doubling of progression-free survival (PFS) associated with their use in hormone receptor-positive, HER2-negative advanced breast cancer (BC), has radically changed the approach to managing this disease. However, resistance to CDK4/6 inhibitors is considered a near-inevitability in most patients. Mechanisms of resistance to these agents are multifactorial, and research in this field is still evolving. Biomarkers with the ability to identify early resistance, or to predict the likelihood of successful treatment using CDK4/6 inhibitors are yet to be identified, and represent an area of unmet clinical need. Here we present selected mechanisms of resistance to CDK4/6 inhibitors, largely focussing on roles of Rb, cyclin E1, and the PIK3CA pathway, with discussion of associated biomarkers which have been investigated and applied in recent pre-clinical and clinical studies. These biological drivers may furthermore influence clinical treatment strategies adopted beyond CDK4/6 resistance.
CDK4/6抑制剂药物的近期问世,使其用于激素受体阳性、HER2阴性晚期乳腺癌(BC)时无进展生存期(PFS)几乎翻倍,这从根本上改变了该病的治疗方法。然而,对大多数患者而言,对CDK4/6抑制剂产生耐药性被认为几乎不可避免。对这些药物产生耐药性的机制是多因素的,该领域的研究仍在不断发展。能够识别早期耐药性或预测使用CDK4/6抑制剂成功治疗可能性的生物标志物尚未确定,这代表了一个未满足的临床需求领域。在此,我们介绍对CDK4/6抑制剂耐药的选定机制,主要聚焦于Rb、细胞周期蛋白E1和PIK3CA通路的作用,并讨论在近期临床前和临床研究中已被研究和应用的相关生物标志物。这些生物学驱动因素可能还会影响CDK4/6耐药之外所采用的临床治疗策略。