Gomes Inês, Abreu Catarina, Costa Luis, Casimiro Sandra
Luis Costa Lab, Instituto de Medicina Molecular, Faculdade de Medicina de Lisboa, Universidade de Lisboa, 1649-028 Lisbon, Portugal.
Oncology Division, Hospital de Santa Maria-Centro Hospitalar Universitário Lisboa Norte, 1649-028 Lisbon, Portugal.
Cancers (Basel). 2023 Oct 2;15(19):4835. doi: 10.3390/cancers15194835.
The approval of cyclin-dependent kinase 4 and 6 inhibitors (CDK4/6i) in combination with endocrine therapy (ET) has remarkably improved the survival outcomes of patients with advanced hormone receptor-positive (HR+) breast cancer (BC), becoming the new standard of care treatment in these patients. Despite the efficacy of this therapeutic combination, intrinsic and acquired resistance inevitably occurs and represents a major clinical challenge. Several mechanisms associated with resistance to CDK4/6i have been identified, including both cell cycle-related and cell cycle-nonspecific mechanisms. This review discusses new insights underlying the mechanisms of action of CDK4/6i, which are more far-reaching than initially thought, and the currently available evidence of the mechanisms of resistance to CDK4/6i in BC. Finally, it highlights possible treatment strategies to improve CDK4/6i efficacy, summarizing the most relevant clinical data on novel combination therapies involving CDK4/6i.
细胞周期蛋白依赖性激酶4和6抑制剂(CDK4/6i)与内分泌治疗(ET)联合应用的获批显著改善了晚期激素受体阳性(HR+)乳腺癌(BC)患者的生存结局,成为这些患者的新的标准治疗方案。尽管这种治疗组合具有疗效,但内在和获得性耐药不可避免地会出现,这是一个重大的临床挑战。已经确定了几种与CDK4/6i耐药相关的机制,包括细胞周期相关机制和细胞周期非特异性机制。本综述讨论了CDK4/6i作用机制的新见解,这些见解比最初认为的更具深远意义,以及目前关于BC中CDK4/6i耐药机制的现有证据。最后,它强调了提高CDK4/6i疗效的可能治疗策略,总结了涉及CDK4/6i的新型联合疗法的最相关临床数据。