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ASH25 Multiple Myeloma

CE / CME

Emerging Data and Clinical Implications in Multiple Myeloma: ASH 2025 Highlights

Physician Assistants/Physician Associates: 1.00 AAPA Category 1 CME credit

Pharmacists: 1.00 contact hour (0.1 CEUs)

Physicians: maximum of 1.00 AMA PRA Category 1 Credit

Nurse Practitioners/Nurses: 1.00 Nursing contact hour

Released: March 05, 2026

Expiration: September 04, 2026

Activity

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Introduction 

In this text-based module, Shaji Kumar, MD, and Sagar Lonial, MD, FACP, FASCO, discuss key findings in multiple myeloma (MM) presented at the 2025 American Society of Hematology (ASH) Annual Meeting. 

The key points discussed in this module are illustrated with thumbnails from the accompanying downloadable PowerPoint slidesets, which can be found here or downloaded by clicking any of the slide thumbnails in the module alongside the expert commentary.  

Please note that Decera Clinical Education plans to measure the educational impact of this activity. Some questions will be asked twice: once at the beginning of the activity, and once again after the discussion that informs the best choice. Your responses will be aggregated for analysis, and your individual responses will not be shared. Thank you in advance for helping us assess the impact of this education. 

Before continuing with this educational activity, please take a moment to answer the following questions.

How many people with MM do you provide care for in a typical month?​

For those who practice in academic or community settings, please indicate your practice setting:

Which of the following bispecific antibody therapies, when used as consolidation therapy after standard CAR T-cell therapy in patients with relapsed/refractory (R/R) MM, was associated with high rates of measurable residual disease (MRD)–negative complete response (CR) at 1 year post CAR T-cell therapy infusion?

In the MajesTEC-3 phase III trial that enrolled patients with previously treated MM, which of the following findings was reported with the combination of daratumumab plus teclistamab compared with a standard daratumumab-based regimen (DPd or DVd)?

You are counseling a patient with R/R MM who has newly documented extramedullary disease (EMD). Based on recently reported results from the RedirecTT-1 trial that evaluated talquetamab plus teclistamab, which of the following would be accurate information to share with them?

You are discussing treatment options with a patient who has standard‑risk relapsed MM who is considering CAR‑T therapy. Based on an analysis of extended outcomes with ciltacabtagene autoleucel (cilta‑cel) in patients with standard‑risk relapsed MM reported by Costa and colleagues at ASH 2025, which of the following would you tell the patient is expected regarding PFS 30 months after CAR T-cell infusion?