Alpelisib for PIK3CA -Mutated, Hormone Receptor–Positive Advanced Breast Cancer

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
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:380 (20): 1929-1940 被引量:2527
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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