医学
泊马度胺
不利影响
地塞米松
耐火材料(行星科学)
内科学
临床终点
多发性骨髓瘤
胃肠病学
随机对照试验
来那度胺
物理
天体生物学
作者
Sikander Ailawadhi,Ivan Špıčka,Andrew Spencer,Lu Jin,Albert Oriol,Silvia Ling,Fredrik Schjesvold,Alejandro Berkovits,Marek Hus,Chunrui Li,Meletios Α. Dimopoulos,Péter Rajnics,Sevgi Kalayoğlu Beşışık,Vânia Hungria,Maria Del Rosario Custidiano,Gurdeep Parmar,Xavier Leleu,Fei Li,Claudio Cerchione,César Cinesi Gómez
摘要
Purpose: To report results of the multicenter, open-label IRAKLIA trial ( NCT05405166 ) of isatuximab subcutaneous (SC) versus intravenous (IV), plus pomalidomide and dexamethasone, in relapsed/refractory multiple myeloma (MM), the first Phase 3 MM trial using an on-body delivery system (OBDS). Methods: Patients with ≥1 prior line of therapy were randomized 1:1 to isatuximab OBDS (1400 mg) or IV (10 mg/kg) weekly in Cycle (C)1, then every 2 weeks, plus pomalidomide (4 mg/day, Day [D]1-21) and dexamethasone (40 mg weekly [age ≥75: 20 mg]) and treated until progression, unacceptable toxicity, or patient request. Co-primary endpoints were overall response rate (ORR; non-inferiority margin, 0.839) and isatuximab C trough (C6D1 predose; non-inferiority margin, 0.8). Non-inferiority of OBDS versus IV was demonstrated if both co-primary endpoints achieved non-inferiority. Results: IRAKLIA randomized 531 patients (OBDS, n=263; IV, n=268). After 12 months median follow-up, ORR was 71.1% (OBDS) and 70.5% (IV; relative risk [95% CI]=1.008 [0.903–1.126]; lower CI exceeded non-inferiority margin). Mean (SD) C6D1 C trough was 499 (259) μg/mL (OBDS) and 340 (169) μg/mL (IV). C trough geometric mean ratio (90% CI) was 1.532 (1.316–1.784); lower CI exceeded non-inferiority margin. Grade ≥3 treatment-emergent adverse event incidences were 81.7% (OBDS) and 76.1% (IV); infusion reaction incidences were 1.5% and 25.0%. Injection site reactions occurred in 0.4% of OBDS injections (all grade 1-2); 99.9% of injections completed without interruption. Conclusion: IRAKLIA demonstrated efficacy and pharmacokinetic non-inferiority between isatuximab OBDS and IV. No unexpected safety signal was observed, with excellent local tolerability of isatuximab OBDS. Efficacy and safety were comparable to isatuximab IV in ICARIA-MM, except the lower OBDS infusion reaction rate. These results support potential use of the OBDS, designed to improve practice efficiency.
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