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Adjuvant lapatinib and trastuzumab for early human epidermal growth factor receptor 2-positive breast cancer: Results From the randomized phase III adjuvant lapatinib and/or trastuzumab treatment optimization trial

机译:辅助拉帕替尼和曲妥珠单抗治疗早期人类表皮生长因子受体2阳性乳腺癌:结果来自随机III期拉帕替尼和/或曲妥珠单抗治疗优化试验

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摘要

Background Lapatinib (L) plus trastuzumab (T) improves outcomes for metastatic human epidermal growth factor 2-positive breast cancer and increases the pathologic complete response in the neoadjuvant setting, but their role as adjuvant therapy remains uncertain. Methods In the Adjuvant Lapatinib and/or Trastuzumab Treatment Optimization trial, patients with centrally confirmed human epidermal growth factor 2-positive early breast cancer were randomly assigned to 1 year of adjuvant therapy with T, L, their sequence (T→L), or their combination (L+T). The primary end point was disease-free survival (DFS), with 850 events required for 80% power to detect a hazard ratio (HR) of 0.8 for L+T versus T. Results Between June 2007 and July 2011, 8,381 patients were enrolled. In 2011, due to futility to demonstrate noninferiority of L versus T, the L arm was closed, and patients free of disease were offered adjuvant T. A protocol modification required P
机译:背景拉帕替尼(L)加上曲妥珠单抗(T)改善了转移性人类表皮生长因子2阳性乳腺癌的结局,并增加了新辅助治疗中的病理完全反应,但其作为辅助治疗的作用仍不确定。方法在辅助性拉帕替尼和/或曲妥珠单抗治疗优化试验中,将具有中心确认的人类表皮生长因子2阳性早期乳腺癌的患者随机分配为接受T,L,其顺序(T→L)或它们的组合(L + T)。主要终点为无病生存期(DFS),L + T与T的危险比(HR)为0.8时,必须有850个事件才能检测到0.8的风险比。结果2007年6月至2011年7月,招募了8,381例患者。 2011年,由于徒劳无功地证明L对T的劣势,L臂被关闭,没有疾病的患者接受了佐剂T的治疗。

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