Landgren Ola, Chari Ajai, Cohen Yael C, Spencer Andrew, Voorhees Peter M, Sandhu Irwindeep, Jenner Matthew W, Smith Dean, Cavo Michele, van de Donk Niels W C J, Beksac Meral, Moreau Philippe, Goldschmidt Hartmut, Vieyra Diego, Sha Linlin, Li Liang, Rousseau Els, Dennis Robyn, Carson Robin, Hofmeister Craig C
Division of Myeloma, Department of Medicine, Sylvester Comprehensive Cancer Center at University of Miami, Miami, FL.
Center of Excellence for Multiple Myeloma, Icahn School of Medicine at Mount Sinai, New York, NY.
Blood. 2025 Apr 10;145(15):1658-1669. doi: 10.1182/blood.2024025897.
Early intervention in smoldering multiple myeloma (SMM) may delay progression to MM. Here, we present the final analysis of the phase 2 CENTAURUS study. In total, 123 patients with intermediate/high-risk SMM were randomized to IV daratumumab 16 mg/kg after a long-intense (n = 41), intermediate (n = 41), or short-intense (n = 41) dosing schedule. At a combined median follow-up of 85.2 months, in the long-intense, intermediate, and short-intense arms complete response or better rates were 4.9%, 9.8%, and 0%; overall response rates were 58.5%, 53.7%, and 37.5%; progressive disease/death rates were 0.096, 0.102, and 0.109 (P < .0001 for all arms); and median progression-free survival was not reached, 84.4, and 74.1 months, respectively. Median overall survival was not reached in any arm. Thirty-six patients in the long-intense or intermediate arms continued daratumumab in an optional extension phase after completing 20 cycles of per-protocol treatment. The median duration of study treatment was 44.0 (range, 1.0-91.6), 35.2 (range, 1.9-90.6), and 1.6 (range, 0.1-1.9) months in the long-intense, intermediate, and short-intense arms, respectively. No new safety signals were observed. With extended follow-up (median, ∼7 years), these data highlight the tolerability of daratumumab and support ongoing trials investigating daratumumab as an early intervention for SMM. This trial was registered at www.ClinicalTrials.gov as #NCT02316106.
对冒烟型多发性骨髓瘤(SMM)进行早期干预可能会延缓其进展为多发性骨髓瘤(MM)。在此,我们展示了2期CENTAURUS研究的最终分析结果。总共123例中/高危SMM患者被随机分配接受静脉注射达雷妥尤单抗,剂量为16 mg/kg,给药方案分为长疗程强化(n = 41)、中疗程(n = 41)或短疗程强化(n = 41)。在合并的中位随访85.2个月时,长疗程强化组、中疗程组和短疗程强化组的完全缓解或更好缓解率分别为4.9%、9.8%和0%;总缓解率分别为58.5%、53.7%和37.5%;疾病进展/死亡率分别为0.096、0.102和0.109(所有组P <.0001);中位无进展生存期未达到、为84.4个月和74.1个月。各治疗组的中位总生存期均未达到。长疗程强化组或中疗程组的36例患者在完成20个周期的按方案治疗后,在一个可选的延长期继续接受达雷妥尤单抗治疗。长疗程强化组、中疗程组和短疗程强化组的研究治疗中位持续时间分别为44.0(范围1.0 - 91.6)、35.2(范围1.9 - 90.6)和1.6(范围0.1 - 1.9)个月。未观察到新的安全信号。随着随访时间延长(中位约7年),这些数据突出了达雷妥尤单抗的耐受性,并支持正在进行的将达雷妥尤单抗作为SMM早期干预措施的试验。该试验已在www.ClinicalTrials.gov注册,注册号为#NCT02316106。