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T-DM1 versus pertuzumab trastuzumab and a taxane as first-line therapy of early-relapsed HER2-positive metastatic breast cancer: an Italian multicenter observational study

机译:T-DM1与PertuzumabTrastuzumab和紫杉烷作为早期复发的Her2阳性转移性乳腺癌的一线治疗:意大利多中心观察研究

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摘要

The current standard first-line treatment of human epidermal growth factor receptor 2 (HER2)-positive (+) metastatic breast cancer is the combination of pertuzumab, trastuzumab and a taxane (P + T + taxane), while standard second-line is ado-trastuzumab-emtansine (T-DM1). The registration trial of pertuzumab, however, did not include early-relapsing patients, defined as patients experiencing tumor relapse ≤12 months from the end of (neo)adjuvant anti-HER2 therapy. Conversely, the pivotal trial of T-DM1 included some patients relapsing ≤6 months after the end of (neo)adjuvant trastuzumab. Thus, a proportion of early-relapsing patients are currently eligible to receive T-DM1 as first-line treatment. Nevertheless, no direct comparison exists between the two regimens in this clinical setting.
机译:当前的人表皮生长因子受体2(HER2) - 阳性(+)转移性乳腺癌的标准第一线治疗是Pertuzumab,Trastuzumab和紫杉烷(P + T +紫杉烷)的组合,而标准的第二行是ADO -trastuzumab-Emtansine(T-DM1)。然而,Pertuzumab的注册试验不包括早期复发患者,定义为在Zer-Her2疗法结束时经历肿瘤复发≤12个月的患者。相反,T-DM1的枢轴试验包括一些患者在(NEO)佐剂曲妥珠单抗结束后复发≤6个月。因此,早期复发患者的比例目前有资格获得T-DM1作为一线治疗。然而,在该临床环境中的两个方案之间没有直接比较。

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