或转移性乳腺癌患者，其中70.5%的受试者曾接受过CDK4/6抑制剂治疗，入组人群高度贴合当前临床真实诊疗场景。研究核心数据展现出突破性治疗获益：LAE002联合氟维司群组的中位PFS达到7.6个月，而安慰剂联合氟维司群组仅为2.0个月，试验组将患者疾病进展或死亡风险大幅降低67%（HR=0.33，p<0.0001），成功达成研究主要终点。安全性方面，LAE002每日一次口服给药的模式耐受性
e passing away of my parents at a very young age. I thought they had become stars in the sky. Mujhe laga woh tara ban chuke hain and they will not be able to see me.” He explained how that loss pushed
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