Scientific Education Hub​

Minimal Residual Disease (MRD) in Myeloma



Purpose statement​

This educational page is meant to provide independent, balanced scientific information on the evolving role of Minimal Residual Disease (MRD) assessment in Multiple Myeloma (MM).​

The aim is to update this page with more information throughout the year to further support healthcare professionals with disease‑state education, peer‑reviewed evidence, and scientific context around MRD methodologies, interpretation challenges, and ongoing research.​


Scientific webinar by Dr. Bruno Paiva​

Minimal Residual Disease (MRD) assessment has become an important topic in Multiple Myeloma research and clinical trials, driven by increasing treatment depth and advances in high‑sensitivity detection techniques, including flow‑ and sequencing‑based approaches, as well as functional and imaging adjuncts.​

​Early data emerging from ongoing clinical studies exploring MRD‑informed treatment strategies, alongside regulatory discussions around its ue as an intermediate endpoint in drug trials and evolving international recommendations by IMWG, EMN and EHA1, 2, continue to shape the role of MRD as a clinical trial endpoint and an evolving tool under investigation in patient management. ​

This webinar by Dr. Bruno Paiva, entitled “Next Generation Flow in Multiple Myeloma Clinical Trials”, reviews key scientific updates and relevant methodological and practical considerations in the context of MRD assessment in Multiple Myeloma.​

1. Kumar S, Paiva B, et al. International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma. Lancet Oncology. 2016.

2. 2. Dimopoulos MA, Terpos E, et al. EHA–EMN evidence‑based guidelines for diagnosis, treatment and follow‑up of patients with multiple myeloma. Nature Reviews Clinical Oncology. 2025

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This site is published by Waters Biosciences’ EMEA Medical and Scientific Affairs team, which is solely responsible for its contents. The material on this site is intended only as informational or as educational aid and is not intended to be taken as medical advice or promotion of any Waters Biosciences’ product. The ultimate responsibility for patient care resides with healthcare professionals.

This information is intended for the use of healthcare professionals in EMEA. Laws, regulatory requirements and medical practices for MRD assessment assays and sharing scientific information may vary among jurisdictions.

Last updated April 10, 2026.

Waters Biosciences Scientific Education Hub
Minimal Residual Disease (MRD) in Myeloma

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in Europe, Middle East and Africa (EMEA).

Medical & Scientific Information intended for healthcare professionals only. Non-promotional. All contents are and should be understood as informative in nature and do not discuss, endorse or recommend any specific test, technology, or clinical action. Not intended for patients.

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