University of California San Francisco Comprehensive Cancer Center, San Francisco, CA
Hope S. Rugo , Fabrice Andre , Gabor Rubovszky , Bella Kaufman , Kenichi Inoue , Masato Takahashi , Satoru Shimizu , Eva M. Ciruelos , Mario Campone , Pier Franco Conte , Hiroji Iwata , Sibylle Loibl , Ingrid A. Mayer , Dejan Juric , Anne-Sophie Longin , David Mills , Celine Wilke , Dalila B. Sellami
Background: Patients (pts) with HR+ breast cancer (BC) often havedysregulatedphosphatidylinositol 3-kinase (PI3K)/mammalian target of rapamycin (mTOR) pathway, which further leads to resistance to endocrine therapy (ET). In a phase 1 study, alpelisib (BYL719), a PI3Kα-specific inhibitor in combination with fulvestrant (FUL) has demonstrated antitumor activity in pts with estrogen receptor-positive, HER2– advanced BC (ABC) with PIK3CA-altered tumors. SOLAR-1 (NCT02437318) aims to assess the efficacy of ALP + FUL in PIK3CA-mutant and non-mutant tumors in HR+, HER2– ABC setting. Methods: SOLAR-1 is a phase 3, randomized, double-blind study conducted in men and postmenopausal women with HR+, HER2– ABC. Pts are randomly (1:1) allocated to oral alpelisib/placebo (300 mg qd) and intramuscular FUL (500 mg) until disease progression or treatment (tx) discontinuation. Stratification factors are presence of liver and/or lung metastases and prior use of CDK4/6 inhibitors. The eligibility criteria for the targeted BC patient population are shown in the Table. The primary endpoint is progression-free survival (PFS; RECIST v1.1; local assessment), while overall survival (OS) is a key secondary endpoint in the PIK3CA-mutant cohort. Other secondary endpoints are PFS and OS in the PIK3CA non-mutant cohort, the association between PFS and baseline PIK3CAstatus in ctDNA, overall response rate, clinical benefit rate, and safety. Recruitment of the planned 560 pts is currently ongoing. Clinical trial information: NCT02437318
Inclusion criteria | Exclusion criteria |
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Locally advanced or metastatic HR+, HER2− BC Recurrence or progression on or after AI therapy Identified PI3K mutational status ≥1 measurable lesion (RECIST v1.1) or predominantly lytic bone lesion ECOG-PS ≤1 | Ineligibility for ET due to symptomatic visceral disease or other disease burden Prior tx with FUL, chemotherapy (except [neo] adjuvant), or PI3K/AKT/mTOR inhibitors Premenopausal status |
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Abstract Disclosures
First Author: Michelino De Laurentiis
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First Author: Dejan Juric