Minimal residual disease (MRD) detection represents a sensitive tool to appropriately measure the response obtained with therapies for multiple myeloma (MM). The achievement of MRD negativity has superseded the conventional complete response (CR) and has been proposed as a surrogate endpoint for progression-free survival and overall survival. Several techniques are available for the detection of MRD inside (next-generation sequencing, flow cytometry) and outside (PET/CT, magnetic resonance) the bone marrow, and their complementary use allows a precise definition of the efficacy of anti-myeloma treatments. This review summarizes MRD data and results from previous clinical trials, highlights open issues related to the role of MRD in MM and discusses how MRD could be implemented in clinical practice to inform on patient prognosis and drive therapeutic decisions.

Minimal Residual Disease in Multiple Myeloma: State of the Art and Future Perspectives

Mina, Roberto
Co-first
;
Oliva, Stefania
Co-first
;
Boccadoro, Mario
Last
2020-01-01

Abstract

Minimal residual disease (MRD) detection represents a sensitive tool to appropriately measure the response obtained with therapies for multiple myeloma (MM). The achievement of MRD negativity has superseded the conventional complete response (CR) and has been proposed as a surrogate endpoint for progression-free survival and overall survival. Several techniques are available for the detection of MRD inside (next-generation sequencing, flow cytometry) and outside (PET/CT, magnetic resonance) the bone marrow, and their complementary use allows a precise definition of the efficacy of anti-myeloma treatments. This review summarizes MRD data and results from previous clinical trials, highlights open issues related to the role of MRD in MM and discusses how MRD could be implemented in clinical practice to inform on patient prognosis and drive therapeutic decisions.
2020
9
7
2142
N/A
https://www.mdpi.com/2077-0383/9/7/2142
https://doi.org/10.3390/jcm9072142
minimal residual disease; multiple myeloma; next-generation flow; next-generation sequencing
Mina, Roberto; Oliva, Stefania; Boccadoro, Mario
File in questo prodotto:
File Dimensione Formato  
Mina et al 2020 - MRD - OA - jcm-09-02142-v2.pdf

Accesso aperto

Descrizione: [Published Vsn.] Mina R et al. J Clin Med . 2020 Aug 13;9(8):2630. doi: 10.3390/jcm9072142. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. Open access article, Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Available at: https://www.mdpi.com/2077-0383/9/7/2142 | https://doi.org/10.3390/jcm9072142 . See also erratum: J Clin Med . 2020 Aug 13;9(8):2630. doi: 10.3390/jcm9082630.
Tipo di file: PDF EDITORIALE
Dimensione 256.34 kB
Formato Adobe PDF
256.34 kB Adobe PDF Visualizza/Apri
ERRATUM of Mina et al 2020 - MRD - OA - jcm-09-02630.pdf

Accesso aperto

Descrizione: [Published Vsn.] Erratum. Mina R et al. J Clin Med . 2020 Aug 13;9(8):2630. doi: 10.3390/jcm9082630. ERRATUM of: Mina R et al. J Clin Med . 2020 Aug 13;9(8):2630. doi: 10.3390/jcm9072142. © 2020 by the authors. Licensee MDPI, Basel, Switzerland. Open access article, Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Available at: https://www.mdpi.com/2077-0383/9/7/2142 | https://doi.org/10.3390/jcm9072142 .
Tipo di file: PDF EDITORIALE
Dimensione 175.61 kB
Formato Adobe PDF
175.61 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1759945
Citazioni
  • ???jsp.display-item.citation.pmc??? 3
  • Scopus 12
  • ???jsp.display-item.citation.isi??? 13
social impact