Department of Oncology, National Taiwan University Hospital, No. 7, Chung Shan South Road, Taipei, 100, Taiwan.
Department of Clinical Oncology, The Chinese University of Hong Kong, Shatin, Hong Kong.
Target Oncol. 2021 Nov;16(6):701-741. doi: 10.1007/s11523-021-00838-x. Epub 2021 Sep 28.
Breast cancer (BC) among Asians accounts for ~ 40% of the global BC burden. Differences in BC risk, presentation, tumor biology, and response to treatment exist between Asian and non-Asian patients; however, Asian patients are often under-represented in clinical trials. This narrative review summarizes the efficacy and safety of pharmacological therapies for BC in Asian populations, with a focus on outcomes in Asian versus non-Asian patients treated with chemotherapy, hormone therapy, anti-human epidermal growth factor receptor-2 targeted therapies, cyclin-dependent kinase 4/6 (CDK4/6) inhibitors, mammalian target of rapamycin inhibitors, bone-targeted therapies, poly-ADP ribose polymerase, phosphoinositide 3-kinase, and checkpoint inhibitors. While most therapies have demonstrated comparable efficacy and safety in Asian and non-Asian patients with BC, differences that are largely attributed to pharmacogenetic variations between populations exist. Pharmacogenetic differences may contribute to a reduced clinical benefit of tamoxifen, whereas improved clinical outcomes have been reported with tyrosine kinase inhibitors and CDK4/6 inhibitors in Asian versus non-Asian patients with BC. In particular, Asian patients have an increased incidence of hematological toxicities, including neutropenia, although adverse events can be effectively managed using dose adjustments. Recent trials with CDK4/6 inhibitors have increased efforts to include Asians within study subsets. Future clinical trials enrolling higher numbers of Asian patients, and an increased understanding of differences in patient and tumor genetics between Asians and non-Asians, have the potential to incrementally improve the management of BC in Asian patients.
亚洲人群乳腺癌(BC)约占全球 BC 负担的 40%。亚洲和非亚洲患者之间存在 BC 风险、表现、肿瘤生物学和治疗反应的差异;然而,亚洲患者在临床试验中往往代表性不足。本综述总结了亚洲人群 BC 药物治疗的疗效和安全性,重点关注了接受化疗、激素治疗、抗人表皮生长因子受体-2 靶向治疗、细胞周期蛋白依赖性激酶 4/6(CDK4/6)抑制剂、哺乳动物雷帕霉素靶蛋白抑制剂、骨靶向治疗、多聚 ADP 核糖聚合酶、磷酸肌醇 3-激酶和检查点抑制剂治疗的亚洲和非亚洲患者的结局。尽管大多数治疗方法在亚洲和非亚洲 BC 患者中均显示出相当的疗效和安全性,但人群之间的药代遗传学差异在很大程度上导致了这些差异。药代遗传学差异可能导致他莫昔芬的临床获益降低,而酪氨酸激酶抑制剂和 CDK4/6 抑制剂在亚洲 BC 患者中的临床获益优于非亚洲患者。特别是,亚洲患者发生血液学毒性(包括中性粒细胞减少症)的发生率增加,尽管可以通过调整剂量来有效管理不良反应。最近的 CDK4/6 抑制剂试验增加了在研究亚组中纳入亚洲人群的努力。未来的临床试验纳入更多的亚洲患者,并深入了解亚洲人和非亚洲患者之间的患者和肿瘤遗传学差异,有可能逐步改善亚洲患者的 BC 管理。