Article Text
Abstract
Introduction Keynote-775 defined the SOC for MMRp recurrent EC. AEs with recommended dosing of lenvatinib/pembrolizumab led to dose reductions in 66.5% of patients. Real world prescription patterns vary significantly from clinical trial. We describe prescribing patterns and outcomes across a multi-institutional consortium.
Methods A national multidisciplinary consortium was utilized to study patients with advanced/recurrent EC treated with lenvatinib/pembrolizumab. Treatment decisions were based on the physician’s recommendation.
Results 217 patients across 14 institutions were identified. Histologic subtypes were 34.1% endometrioid, 39.6% serous, 9.7% carcinosarcoma, 10.1% mixed, and 2.8% clear cell. 82.9% were MMRp and 4.6% were MMRd. Median dose intensity of lenvatinib was 14 mg. Lenvatinib starting dose was 20 mg in 17.1%, 18 mg in 12.9%, 14 mg in 41%, 10 mg in 15.7%. Rates of any grade >=3 AE related to lenvatinib were 20 mg (13.5%), 18 mg (17.9%), 14 mg (7.9%), 10 mg (17.6%) (p=0.31). Pembrolizumab dosing was 200 mg Q3W in 85.6% and 400 mg Q6W in 6.5%. ORR (p=0.38), PFS (p=0.97) & OS (p=0.31) were similar in White vs. Black patients. ORR in relation to Lenvatinib starting dose 20 mg, 18 mg, 14 mg, 10 mg was 27%, 35.7%, 39.3%, 44.1% (p=0.08). In relation to Lenvatinib starting dose, 12-month PFS rates were 40%, 35%, 35%, 47% respectively (p=0.92), 12-month OS were 59%, 66%, 56%, 51% respectively (p=0.79), and median duration of therapy was 5.1, 4.1, 4.8, 4.6 months respectively (p=0.52).
Conclusion/Implications In a real-world analysis, the predominant starting dose is 14 mg lenvatinib and 200 mg pembrolizumab. Grade >=3 AE’s, 12-month PFS/OS, ORR & duration of therapy related to lenvatinib starting dose were not statistically different.