Authors
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How JA, Westin SN, Pham M, Lawson B, Chen M, Tandon N, Yuan Y, Zhang R, Jazaeri AA, Sood AK, Onstad Grinsfelder M, Schmeler KM, Vining DJ, Fix SM, Dai Y, Bowen MB, Lu KH, Yates MS, Broaddus R, Soliman PT -More
Category
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Primary study
Journal»Nature communications
Year
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2026
In this phase II trial, patients with endometrial cancer (EC) were randomized to everolimus/letrozole with (experimental arm) or without ribociclib (control arm) (ClinicalTrials.gov Identifier: NCT03008408). The primary endpoint was progression-free survival (PFS). Secondary endpoints included toxicity, overall survival (OS), objective response rate (ORR), and clinical benefit rate (CBR). For all-comers, there was no difference in PFS (HR 0.78, 95% CI 0.4-1.4, p = 0.38), OS (HR 0.8, 95% CI 0.4-1.5, p = 0.46), ORR (44.1% vs 25.7%, p = 0.11), or toxicity-related treatment discontinuation (4 [8.6%] vs 3 [11.4%], p = 0.22). Among those with prior endocrine therapy, ORR was higher in the experimental arm (61.5% vs 0.0%, p < 0.001). Within the experimental arm, CTNNB1mut tumors were associated with improved PFS (HR 0.27, 95% CI 0.1-0.7, p = 0.006) and OS (HR 0.24, 95% CI 0.1-0.7, p = 0.004) compared to those with non-CTNNB1mut tumors. Despite no survival improvement in all-comers, addition of ribociclib to everolimus/letrozole may improve efficacy in patients with prior endocrine therapy and cases with CTNNB1mut tumors may have prolonged response.
Epistemonikos ID: 8419af8cbadb0c49251fedd6a2f14fa6e491be79
First added on: Oct 02, 2026