医学
乳腺癌
激素受体
癌症
肿瘤科
激素
人表皮生长因子受体2
癌症研究
内科学
受体
内分泌学
作者
Fabrice André,Eva Ciruelos,Gábor Rubovszky,Mario Campone,Sibylle Loibl,Hope S. Rugo,Hiroji Iwata,Pierfranco Conté,Ingrid A. Mayer,Bella Kaufman,Toshinari Yamashita,Yen‐Shen Lu,Kenichi Inoue,Masato Takahashi,Zsuzsanna Pápai,Anne-Sophie Longin,David Mills,Celine Wilke,Samit Hirawat,Dejan Juric
标识
DOI:10.1056/nejmoa1813904
摘要
BACKGROUND: mutations occur in approximately 40% of patients with hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative breast cancer. The PI3Kα-specific inhibitor alpelisib has shown antitumor activity in early studies. METHODS: -mutated cancer. Secondary end points included overall response and safety. RESULTS: -mutated cancer was greater with alpelisib-fulvestrant than with placebo-fulvestrant (26.6% vs. 12.8%); among patients with measurable disease in this cohort, the percentages were 35.7% and 16.2%, respectively. In the overall population, the most frequent adverse events of grade 3 or 4 were hyperglycemia (36.6% in the alpelisib-fulvestrant group vs. 0.7% in the placebo-fulvestrant group) and rash (9.9% vs. 0.3%). Diarrhea of grade 3 occurred in 6.7% of patients in the alpelisib-fulvestrant group, as compared with 0.3% of those in the placebo-fulvestrant group; no diarrhea of grade 4 was reported. The percentages of patients who discontinued alpelisib and placebo owing to adverse events were 25.0% and 4.2%, respectively. CONCLUSIONS: -mutated, HR-positive, HER2-negative advanced breast cancer who had received endocrine therapy previously. (Funded by Novartis Pharmaceuticals; SOLAR-1 ClinicalTrials.gov number, NCT02437318.).
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