Ludek Pour, Sosana Delimpasi, Wojciech Legiec, Jiri Minarik, Ivan Spicka, Sebastian Grosicki, Marcin Rymko, Jacek Najda, Argiris Symeonidis, Birgitta Andersson, Gunilla Huledal, Stefan Norin, Meletios-Athanasios Dimopoulos
BACKGROUND: Information about safety and pharmacokinetics (PK) of melflufen (melphalan flufenamide) is limited in renal impairment (RI) patients. The BRIDGE study evaluated the impact of renal function on PK of the main alkylating agent of melflufen, melphalan, and assessed the safety of melflufen plus dexamethasone in relapsed/refractory multiple myeloma (RRMM) patients. METHODS: ) RI. Patients received melflufen 20 to 40 mg intravenously every 28 days, plus weekly dexamethasone 40 mg. Three post-infusion blood samples were collected in Cycles 1 and 2. Primary endpoints were safety and melphalan PK. RESULTS: were lower in Cohort 1b (472.2 ng/mL and 1286.2 h·ng/mL, respectively) and Cohort 2a (181.2 ng/mL and 528.5 h·ng/mL, respectively) compared to Cohort 1a (550.2 ng/mL and 1418.7 h·ng/mL, respectively). Mean elimination half-life increased slightly with declining renal function (Cohort 1a to 2a: 89.1-109.6 min). Treatment-emergent adverse events occurred in 34 patients and 6 patients died due to a treatment-emergent adverse events. CONCLUSIONS: PK results from the BRIDGE study support the recommended dose of melflufen 30 mg for moderate RI patients. No new safety signals were reported in RRMM patients with moderate-to-severe RI.