de Arriba de la Fuente Felipe, Gironella Mesa Mercedes, Hernández García Miguel Teodoro, Soler Campos Juan Alonso, Herráez Rodríguez Susana, Moreno Belmonte María José, Regueiro López Teresa, González-Pardo Miriam, Casanova Espinosa María
Hematology Department, Hospital Universitario Morales Meseguer, IMIB-Pascual Parrilla, Universidad de Murcia, 30008 Murcia, Spain.
Hematology Department, Hospital Universitario Vall d'Hebrón, 08035 Barcelona, Spain.
Pharmaceuticals (Basel). 2024 Sep 26;17(10):1272. doi: 10.3390/ph17101272.
Real-world evidence on the impact of monoclonal antibodies as first-line treatment in Spain is limited. This observational, retrospective and prospective, multicenter, descriptive study included 117 transplant-ineligible newly diagnosed multiple myeloma (TIE-NDMM) patients divided into Group A, who received no daratumumab standard regimens, and the DVMP group (daratumumab, bortezomib, melphalan, and prednisone treatment). More than 90% of the patients in Group A received bortezomib, lenalidomide, or a combination of them. The median follow-up time for Group A was 38.2 months in comparison to 25.8 months for the DVMP group ( < 0.0001). The rate of DVMP patients that experienced disease progression or death from any cause was 36.8%, compared to 67.3% of Group A patients at 36 months of follow-up. The DVMP group had a higher 36-month progression-free survival (PFS) rate (52.9% vs. 31.7%). During the retrospective period, 73.0% of patients reported adverse drug reactions, while in the prospective period, 40.5% experienced adverse events, with no clinical differences between groups. The study supports the use of daratumumab regimens in frontline therapy based on real-world data. The findings provide valuable insights into the clinical outcomes of daratumumab therapy, which can help physicians make informed decisions regarding the optimal treatment approach for this patient population.
关于单克隆抗体作为西班牙一线治疗手段的影响,现实世界证据有限。这项观察性、回顾性和前瞻性、多中心描述性研究纳入了117例不符合移植条件的新诊断多发性骨髓瘤(TIE-NDMM)患者,分为A组(未接受达雷妥尤单抗标准方案)和DVMP组(达雷妥尤单抗、硼替佐米、美法仑和泼尼松治疗)。A组超过90%的患者接受了硼替佐米、来那度胺或两者联合治疗。A组的中位随访时间为38.2个月,而DVMP组为25.8个月(<0.0001)。随访36个月时,DVMP组出现疾病进展或因任何原因死亡的患者比例为36.8%,而A组为67.3%。DVMP组的36个月无进展生存期(PFS)率更高(52.9%对31.7%)。回顾期内,73.0%的患者报告了药物不良反应,而在前瞻期,40.5%的患者经历了不良事件,两组之间无临床差异。该研究支持基于现实世界数据在一线治疗中使用达雷妥尤单抗方案。这些发现为达雷妥尤单抗治疗的临床结果提供了有价值的见解,有助于医生就该患者群体的最佳治疗方法做出明智决策。