
Saad Usmani
Articles
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1 month ago |
nature.com | Philippe Moreau |Katja Weisel |Hartmut Goldschmidt |Saad Usmani |Robert Orlowski |Nizar Bahlis | +7 more
AbstractIn the MAIA study, daratumumab plus lenalidomide and dexamethasone (D-Rd) improved progression-free survival (PFS) and overall survival (OS) versus lenalidomide and dexamethasone (Rd) alone in transplant-ineligible patients with newly diagnosed multiple myeloma (NDMM). We report updated efficacy and safety from MAIA (median follow-up, 64.5 months), including a subgroup analysis by patient age (<70, ≥70 to <75, ≥75, and ≥80 years).
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Jan 10, 2025 |
businessandamerica.com | Saad Usmani
Video content above is prompted by the following:Provide a brief overview of the CEPHEUS study and the expanded analysis of MRD outcomes presented at ASH 2024. What was the objective of this study? How was this study designed/what methodology was used? What additional MRD outcomes were presented? Source link
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Jan 10, 2025 |
ajmc.com | Saad Usmani
OpinionVideoJanuary 10, 2025Author(s):Saad Z. Usmani, MD, MBA, FACP, discusses how the definition of the transplant-ineligible population for multiple myeloma is evolving while also addressing the challenges of standardizing minimal residual disease (MRD) as a biomarker across various treatment settings and clinical trials to ensure consistent and reliable use in treatment decision-making.
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Jan 10, 2025 |
ajmc.com | Saad Usmani
OpinionVideoJanuary 10, 2025Author(s):Saad Z. Usmani, MD, MBA, FACP, discusses how the CEPHEUS study, presented at ASH 2024, along with its expanded analysis of minimal residual disease (MRD) outcomes, provides valuable insights into the role of MRD as a biomarker in multiple myeloma treatment, highlighting its potential to guide therapy decisions and improve patient outcomes.
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Jan 2, 2025 |
ajmc.com | Saad Usmani
OpinionVideoJanuary 2, 2025Author(s):Saad Z. Usmani, MD, MBA, FACP, discusses how the MajesTEC-5 study, presented at ASH 2024, demonstrates the potential of teclistamab in combination with standard therapy in the frontline setting, highlighting its safety profile and 100% minimal residual disease (MRD) negativity after cycle 3, and explores how using bispecific antibodies like teclistamab earlier in treatment could influence future options for relapsed/refractory multiple myeloma.
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