Minimal Residual Disease Significance in Multiple Myeloma Patients Treated with Anti-CD38 Monoclonal Antibodies

被引:0
|
作者
Caroni, Federico [1 ]
Sammartano, Vincenzo [1 ]
Pacelli, Paola [1 ]
Sicuranza, Anna [1 ]
Malchiodi, Margherita [1 ]
Dragomir, Andreea [1 ]
Ciofini, Sara [1 ]
Raspadori, Donatella [1 ]
Bocchia, Monica [1 ]
Gozzetti, Alessandro [1 ]
机构
[1] Univ Siena, AOUS Policlin Le Scotte, I-53100 Siena, Italy
关键词
multiple myeloma; minimal residual disease; monoclonal antibodies; TRANSPLANT-ELIGIBLE PATIENTS; STEM-CELL TRANSPLANTATION; OPEN-LABEL; DRUG-RESISTANCE; FINAL ANALYSIS; DARATUMUMAB; DEXAMETHASONE; LENALIDOMIDE; THERAPY; BORTEZOMIB;
D O I
10.3390/ph18020159
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Minimal residual disease (MRD) evaluation is a recognized endpoint in clinical trials. Both next-generation flow and sequencing could be used as complementary techniques to detect myeloma cells after therapy to measure the depth of response and novel drug efficacy. Anti-CD38 monoclonal antibodies combined with proteasome inhibitors and immunomodulatory drugs have increased the quality of response in myeloma patients, and MRD evaluation is also entering routine clinical practice in many hematological centers. This review analyzes updated results from recent clinical trials utilizing anti-CD38 monoclonal antibodies such as isatuximab and daratumumab in terms of their responses and MRD data. MRD-driven therapy appears promising for the future of MM patients, and emerging minimally invasive techniques to assess MRD are under investigation as novel potential methods to replace or integrate traditional MRD evaluation.
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页数:17
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