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ASH 2024 | What do community oncologists need to know about using MRD in multiple myeloma?
In this video, Bruno Paiva, PhD, University of Navarra, Pamplona, Spain, briefly comments on the importance of adhering to guidelines when using measurable residual disease (MRD) as a biomarker in multiple myeloma (MM), emphasizing that compliance with methodology, sample quality, and data interpretation is crucial to achieving optimal patient outcomes. This interview took place at the 66th ASH Annual Meeting and Exposition, held in San Diego, CA.
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Transcript (AI-generated)
Now that MRD is becoming so important in myeloma, both in terms of primary endpoint in clinical trials, but also potentially as a biomarker driving treatment decisions, my take-home message is to comply with the guidelines. If we are using more and more MRD in routine practice, please adhere to the guidelines in terms of methodology, sample quality, and data interpretation...
Now that MRD is becoming so important in myeloma, both in terms of primary endpoint in clinical trials, but also potentially as a biomarker driving treatment decisions, my take-home message is to comply with the guidelines. If we are using more and more MRD in routine practice, please adhere to the guidelines in terms of methodology, sample quality, and data interpretation. This is paramount to achieve the best outcomes using MRD as a biomarker.
This transcript is AI-generated. While we strive for accuracy, please verify this copy with the video.
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Disclosures
Bristol Myers Squibb/Celgene, Janssen, Sanofi, and Takeda: Consultancy; Adaptive, Amgen, Becton Dickinson, Bristol Myers Squibb/Celgene, Janssen, Merck, Novartis, Roche, Sanofi and Takeda: Honoraria; Aztra Zeneca, Bristol Myers Squibb/Celgene, EngMab, Roche, Sanofi, and Takeda: Research Funding.
