Abstract Background: Patients with gastric cancer, biliary tract cancer (BTC), and pancreatic ductal adenocarcinoma (PDAC) have poor survival outcomes and limited second- or later-line treatment options. Certain drugs targeting vascular endothelial growth factor (VEGF) or programmed cell death protein 1 (PD-1) signaling pathways are currently used in these cancers in specific circumstances; however, there remains a need for novel treatment combinations. LEAP-005 is a multicohort, open-label, phase 2 study that evaluated lenvatinib (multitargeted inhibitor of tyrosine kinases, including VEGF) plus pembrolizumab (anti‒PD-1 monoclonal antibody) in select previously treated solid tumors. Methods: Participants with previously treated, advanced gastric cancer, BTC, and PDAC were enrolled in cohorts C, F, and G of LEAP-005, respectively, and received lenvatinib 20 mg/day orally plus pembrolizumab 200 mg intravenously every 3 weeks. Primary endpoints were objective response rate (ORR) and safety. Results: Of 99, 102, and 103 total participants enrolled in cohorts C, F, and G, respectively, median times from first dose of study treatment to data cutoff (February 6, 2023) were 23.7, 24.2, and 19.5 months. ORRs (95% CI) by blinded independent central review were 15.2% (8.7%‒23.8%) in cohort C, 17.6% (10.8%‒26.4%) in cohort F, and 7.8% (3.4%‒14.7%) in cohort G. Grade 3‒5 treatment-related adverse events occurred in 54.5% of participants in cohort C, and grade 3‒4 (no grade 5) occurred in 60.8% and 59.2% of participants in cohorts F and G, respectively. Conclusion: Lenvatinib plus pembrolizumab demonstrated modest antitumor activity and a manageable safety profile in previously treated, advanced gastric cancer, BTC, and PDAC.
Ponz-Sarvise et al. (Thu,) studied this question.
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