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经过大约15个月的额外随访,palbociclib联合来曲唑在整体人群及所有患者亚组中,较安慰剂加来曲唑持续显示出更优的无进展生存期(PFS),同时安全性特征依然良好,生活质量得以维持。这些数据确认,palbociclib-来曲唑应被视为ER+/HER2-晚期乳腺癌患者,包括低疾病负荷或长无病间期患者的一线治疗标准。由Pfizer资助;临床试验注册号:NCT01740427。
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Hope S. Rugo
Richard S. Finn
Véronique Dièras
Breast Cancer Research and Treatment
University of California, Los Angeles
University of California, San Francisco
University of Alberta
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Rugo等人(周四)研究了这一问题。
www.synapsesocial.com/papers/69d8d9b0d2f7327e70ae46b3 — DOI: https://doi.org/10.1007/s10549-018-05125-4
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