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Review
. 2024 Apr;38(2):477-495.
doi: 10.1016/j.hoc.2023.12.009. Epub 2024 Jan 6.

Measurable Residual Disease and Decision-Making in Multiple Myeloma

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Review

Measurable Residual Disease and Decision-Making in Multiple Myeloma

Benjamin A Derman et al. Hematol Oncol Clin North Am. 2024 Apr.

Abstract

Measurable (minimal) residual disease (MRD) has already proven to be one of the most important prognostic factors in multiple myeloma (MM). Each improvement in the depth of MRD testing has led to superior discrimination of outcomes, and sustained MRD negativity seems to be paramount to durable responses. Peripheral blood assays to assess for MRD are still under investigation but hold promise as complementary tools to bone marrow MRD assays such as next-generation sequencing and flow cytometry. Herein, the authors explore the evidence and potential benefits and drawbacks of MRD-adapted clinical decision-making in MM.

Keywords: MRD; Measurable residual disease; Minimal residual disease; Multiple myeloma.

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Conflict of interest statement

Disclosure B.A. Derman declares consultancy for COTA Inc, GLG Consulting, Guidepoint, Janssen, and PRECISIONheor; honoraria from the American Physician Institute, Multiple Myeloma Research Foundation, and Plexus Communications; independent clinical trial reviewer for BMS. R. Fonseca declares consultancy for AbbVie, Adaptive Biotechnologies, AMGEN, AZeneca, Bayer, Binding Site, BMS (Celgene), Millenium Takeda, Jansen, Juno, Kite, Merck, Pfizer, Pharmacyclics, Regeneron, Sanofi; scientific advisory boards for Adaptive Biotechnologies, Caris Life Sciences, Oncotracker; board of directors for Antegene, AZBio; and patents for FISH in myeloma.

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