Measurable residual disease in multiple myeloma: ready for clinical practice?

被引:0
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作者
Leire Burgos
Noemi Puig
Maria-Teresa Cedena
María-Victoria Mateos
Juan José Lahuerta
Bruno Paiva
Jesús F. San-Miguel
机构
[1] Instituto de Investigación Sanitaria de Navarra (IDISNA),Clínica Universidad de Navarra, Centro de Investigación Médica Aplicada (CIMA)
[2] CIBER-ONC number CB16/12/00369,Hospital Universitario de Salamanca
[3] Instituto de Investigación Biomédica de Salamanca (IBSAL),undefined
[4] Hospital 12 de Octubre,undefined
[5] CIBER-ONC number CB16/12/00369,undefined
关键词
Myeloma; Plasma cells; MRD; Clinical practice; Surrogate;
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摘要
The landscape of multiple myeloma (MM) has changed considerably in the past two decades regarding new treatments, insight into disease biology and innovation in the techniques available to assess measurable residual disease (MRD) as the most accurate method to evaluate treatment efficacy. The sensitivity and standardization achieved by these techniques together with unprecedented rates of complete remission (CR) induced by new regimens, raised enormous interest in MRD as a surrogate biomarker of patients’ outcome and endpoint in clinical trials. By contrast, there is reluctance and general lack of consensus on how to use MRD outside clinical trials. Here, we discuss critical aspects related with the implementation of MRD in clinical practice.
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