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Fulvestrant in Combination with CDK4/6 Inhibitors for HER2- Metastatic Breast Cancers: Current Perspectives

机译:氟斯特提与HER2-转移性乳腺癌的CDK4 / 6抑制剂组合:当前的观点

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The development of CDK 4/6 inhibitors has dramatically changed the therapeutic management of hormone receptor-positive (HR+) and HER2 negative metastatic breast cancer (MBC). In combination with fulvestrant, palbociclib, ribociclib and abemaciclib have each been approved for HR+/HER2- MBC following the results of randomized Phase III studies (PALOMA-3, MONALEESA-3, MONARCH-2) and shown a significant advantage in PFS. Data from clinical trials support the combination with aromatase inhibitors in the first line setting and with fulvestrant in the second line. Each agent is well tolerated, and most of the toxicities observed with this class of drugs are generally easily manageable and free from particular complications. The latest evidence from MONARCH-2 and MONALEESA-3 trials shows benefits in terms of overall survival (OS), suggesting an option of using fulvestrant in combination with CDK 4/6 inhibitors in the first line setting. Additional research is needed to determine optimal treatment sequencing, understand the mechanisms of resistance, and develop novel therapeutic strategies to overcome clinical resistance and further improve the outcomes of patients with HR+/HER- MBC. Key questions in the field include the further impact on progression-free survival, overall survival, and the role of continuing CDK 4/6 blockade beyond progression. The purpose of this review is to describe the clinical relevance of fulvestrant in combination with CDK 4/6 inhibitors in HR+/HER2- MBC patients, as well as to discuss the current controversies and evolving research areas.
机译:CDK 4/6抑制剂的发展大大改变了激素受体阳性(HR +)和HER2阴性转移性乳腺癌(MBC)的治疗管理。结合氟斯特语,帕尔巴昔米菌,核苷酸和ABEMACICLIB在随机期III研究(Paloma-3,MonaleESA-3,Monarch-2)的结果后,每次被批准为HR + / HER2-MBC,并在PFS中显示出显着的优势。来自临床试验的数据支持第一线设置中与芳香酶抑制剂的组合,并在第二线中用富勒斯特。每个试剂耐受良好耐受,并且随着这类药物观察到的大多数毒物通常易于管理,并且没有特别的并发症。来自Monarch-2和Monaleesa-3试验的最新证据表明了在整体存活(OS)方面的益处,表明在第一线设置中使用氟斯特提结合CDK 4/6抑制剂。需要进行额外的研究来确定最佳治疗测序,了解抵抗机制,以及开发新的治疗策略,以克服临床抗性,进一步改善HR + / HER-MBC患者的结果。该领域的关键问题包括进一步影响无进展的生存,整体生存率,以及继续CDK 4/6封锁超越进展的作用。本综述的目的是描述氟斯特朗特与人力资源+ / HER2-MBC患者CDK 4/6抑制剂组合的临床相关性,以及讨论目前的争论和不断发展的研究领域。

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