Adis, a Wolters Kluwer Business, Auckland, New Zealand.
Drugs. 2010 Jul 30;70(11):1411-22. doi: 10.2165/11204550-000000000-00000.
Lapatinib is an orally active, low molecular weight, reversible inhibitor of the intracellular tyrosine kinase domains of both human epidermal growth factor receptor (HER) type 1 (HER1) and type 2 (HER2). In a large phase III trial (EGF30008) in 1286 postmenopausal women with hormone receptor (HR)-positive, metastatic breast cancer who had not received previous therapy for advanced or metastatic disease, the primary endpoint of median progression-free survival in a HER2-positive population of 219 women was significantly longer with lapatinib plus letrozole than with letrozole plus placebo (8.2 vs 3.0 months). Overall response rates (28% vs 15%) and clinical benefit rates (responsive or stable disease for >or=6 months; 48% vs 29%) were also significantly higher with lapatinib plus letrozole than with letrozole plus placebo. Most adverse events associated with lapatinib when administered in combination with letrozole were mild to moderate in severity in the EGF30008 phase III trial.
拉帕替尼是一种口服活性、低分子量、可逆的人表皮生长因子受体(HER)1 型(HER1)和 2 型(HER2)细胞内酪氨酸激酶结构域抑制剂。在一项针对 1286 例绝经后 HR 阳性、转移性乳腺癌患者的大型 III 期试验(EGF30008)中,这些患者既往未接受过晚期或转移性疾病的治疗,219 例 HER2 阳性患者的中位无进展生存期的主要终点与拉帕替尼联合来曲唑相比,来曲唑联合安慰剂显著延长(8.2 个月 vs 3.0 个月)。拉帕替尼联合来曲唑的总缓解率(28% vs 15%)和临床获益率(缓解或疾病稳定 > 或 = 6 个月;48% vs 29%)也显著高于来曲唑联合安慰剂。在 EGF30008 期 III 试验中,拉帕替尼联合来曲唑治疗时,大多数与拉帕替尼相关的不良反应严重程度为轻度至中度。