Unravelling Transplant-Ineligible Newly Diagnosed Multiple Myeloma Treatment in Real-World Practice in Spain: The CARINAE Study

被引:0
作者
de la Fuente, Felipe de Arriba [1 ]
Mesa, Mercedes Gironella [2 ]
Garcia, Miguel Teodoro Hernandez [3 ]
Campos, Juan Alonso Soler [4 ]
Rodriguez, Susana Herraez [5 ]
Belmonte, Maria Jose Moreno [6 ]
Lopez, Teresa Regueiro [7 ]
Gonzalez-Pardo, Miriam [8 ]
Espinosa, Maria Casanova [9 ]
机构
[1] Univ Murcia, Hosp Univ Morales Meseguer, Hematol Dept, IMIB Pascual Parrilla, Murcia 30008, Spain
[2] Hosp Univ Vall dHebron, Hematol Dept, Barcelona 08035, Spain
[3] Hosp Univ Canarias, Hematol Dept, San Cristobal la Laguna 38320, Spain
[4] Hosptial Univ Parc Tauli, Hematol Dept, Barcelona 08208, Spain
[5] Hosp Univ Basurto, Hematol Dept, Bilbao 48013, Spain
[6] Hosp Univ Virgen Arrixaca, Hematol Dept, Murcia 30120, Spain
[7] Spanish Multiple Myeloma Patient Community CEMMP, Leon 24560, Spain
[8] Johnson & Johnson Co, Med Dept, Janssen Cilag SA, Madrid 28042, Spain
[9] Hosp Costa Sol, Dept Hematol Clin Oncol, Marbella 29603, Spain
关键词
multiple myeloma; monoclonal antibodies; immunotherapy; chemotherapy; daratumumab; DARATUMUMAB; DEXAMETHASONE; BORTEZOMIB; LENALIDOMIDE; PREDNISONE; MELPHALAN; THERAPY; CARE;
D O I
10.3390/ph17101272
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
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 (p < 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.
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页数:16
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