Matthew A. Powell, Henrik Roed, Lyndsay Willmott, David Cibula, Destin Black, Giorgio Valabrega, Sudarshan Sharma, Stefan Kommoss, Lisa M. Landrum, Ingrid Boere, Cara Mathews, Vladyslav Sukhin, M. Gold, Caroline Lundgren, Sarah Gill, Lucy Gilbert, Ilana Cass, Mitchell I. Edelson, Joseph Buscema, Nicole S. Nevadunsky, Kari Ring, Bhavana Pothuri, Helen D. Eshed, Carolyn McCourt, Robert L. Coleman, Matthew Grimshaw, Laura Austin, Magdalena Zając, Brian Slomovitz, Trine Nøttrup
OBJECTIVE: Dostarlimab+carboplatin-paclitaxel (CP) demonstrated significant improvement in progression-free survival (PFS) and clinically meaningful improvement in overall survival (OS) vs CP alone among patients with dMMR/MSI-H primary advanced/recurrent endometrial cancer (EC) in Part 1 of the randomized phase 3 RUBY trial (NCT03981796). We report updated efficacy and safety data with approximately 4 years of follow-up. METHODS: Patients were randomized 1:1 to receive dostarlimab+CP or placebo+CP followed by dostarlimab or placebo up to 3 years or until disease progression. Descriptive analyses of OS and PFS were conducted in the dMMR/MSI-H population (median follow-up, 55.6 months). Post hoc conditional survival analyses and a mixture cure model (MCM) fitted to PFS data to estimate the proportion of patients who had curative potential are presented to provide prognostic insights into long-term survival. RESULTS: Dostarlimab+CP demonstrated sustained OS and PFS benefits. Median PFS and OS were not reached with a 66% reduction in risk of death vs placebo+CP. PFS curve plateauing (only 4 progression events with additional 2.5 years follow-up since the previous PFS analysis at interim analysis 1) demonstrated durable disease control. Patients alive at the 1- and 2-year landmarks had >80% probability of remaining alive an additional 3 and 2 years, respectively. At 4 years, the MCM analysis estimated a cure rate with dostarlimab of 54% (95% CI 35%-72%). No new safety signals were observed. CONCLUSIONS: At 4 years, RUBY demonstrated sustained remission and long-term survival benefit, suggesting the potential for curative intent with dostarlimab+CP in patients with dMMR/MSI-H primary advanced or recurrent EC.