Alpelisib for <i>PIK3CA</i> -Mutated, Hormone Receptor–Positive Advanced Breast Cancer

Fabrice André(Université Paris-Sud), Eva Ciruelos, Gábor Rubovszky(National Institute of Oncology), Mario Campone(Institut de Cancérologie de l'Ouest), Sibylle Loibl(German Breast group), Hope S. Rugo(UCSF Helen Diller Family Comprehensive Cancer Center), Hiroji Iwata(Aichi Cancer Center), Pierfranco Conté(University of Padua), Ingrid A. Mayer(Vanderbilt University), Bella Kaufman(Sheba Medical Center), Toshinari Yamashita(Kanagawa Cancer Center), Yen‐Shen Lu(National Taiwan University Hospital), Kenichi Inoue(Saitama Cancer Center), Masato Takahashi(National Hospital Organization Hokkaido Medical Center), Zsuzsanna Pápai(Buda Health Center), Anne-Sophie Longin(Novartis (Switzerland)), David Mills(Novartis (Switzerland)), Celine Wilke(Novartis (Switzerland)), Samit Hirawat, Dejan Juric(Massachusetts General Hospital)
New England Journal of Medicine
May 15, 2019
Cited by 2,550Open Access
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Abstract

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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