CDK4/6抑制剂:为hr阳性,her2阴性早期乳腺癌铺平道路

Kristi Orbaugh, RN, MSN, RNP, AOCN, Val R. Adams, PharmD, FCCP, BCOP, FHOPA, Theresa W. Gillespie, PhD, MA, RN, FAAN
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引用次数: 0

摘要

细胞周期蛋白依赖性激酶(CDK) 4/6抑制剂正在彻底改变晚期和转移性激素受体阳性(HR+)和人表皮生长因子受体2阴性(HER2 -)乳腺癌患者的护理。这些口服药物通常与其他激素治疗相结合,在临床试验中取得了相当大的成功,并广泛用于肿瘤学实践。CDK4/6抑制剂也被研究用于治疗早期HR+、HER2 -乳腺癌。与单独的内分泌治疗相比,在HR+、HER2 -、淋巴结阳性、高危早期乳腺癌患者中,abemaciclib加入辅助内分泌治疗可提高侵袭性无病生存期和远处无复发生存期,目前已被fda批准作为辅助治疗。在这里,我们回顾了最近支持CDK4/6抑制剂在早期和转移性乳腺癌中使用的临床数据。此外,专家小组将讨论实用策略,以促进和改善口服CDK4/6抑制剂治疗患者的依从性和副作用管理。
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CDK4/6 Inhibitors: Paving the Way for HR-Positive, HER2-Negative Early Breast Cancer
Cyclin-dependent kinase (CDK) 4/6 inhibitors are revolutionizing care for patients with advanced and metastatic hormone receptor–positive (HR+) and human epidermal growth factor receptor 2–negative (HER2–) breast cancer. These oral agents, often combined with other hormone-based therapy, have demonstrated considerable success in clinical trials and are used widely in oncology practices. CDK4/6 inhibitors are also being investigated for the treatment of early stage HR+, HER2– breast cancer. The addition of abemaciclib to adjuvant endocrine therapy improved invasive disease-free survival and distant relapse-free survival compared with endocrine therapy alone in patients with HR+, HER2–, node-positive, high-risk early breast cancer, and is now FDA-approved as adjuvant treatment in this setting. Here we review recent clinical data supporting the use of CDK4/6 inhibitors in both early and metastatic breast cancer. In addition, an expert faculty panel will discuss practical strategies to promote and improve adherence and side effect management in patients being treated with oral CDK4/6 inhibitors.
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