In separate, live virtual events, Doris Hansen, MD, and Leyla O. Shune, MD, discuss options for a patient with relapsed/refractory multiple myeloma and how often participants use chimeric antigen receptor (CAR) T-cell therapy.
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CASE SUMMARY
A 60-year-old man who was diagnosed 3 years ago with lenalidomide-refractory IgG kappa multiple myeloma and translocation(14;16) presented to his oncologist at first relapse.
He lived in a rural community.
Medical history: hypertension controlled with lisinopril
He received previous treatments with:
D-VRd (daratumumab [Darzalex], bortezomib [Velcade], lenalidomide [Revlimid], and dexamethasone) followed by autologous stem cell transplant (ASCT) with lenalidomide maintenance
Achieved very good partial response post ASCT
Patient complained of excessive fatigue and low back pain exacerbated by movement.
ECOG performance status: 0
Weight, 170 lb (down 15 lb in last 4 months)
Biopsy
Bone marrow plasma cells: 20%
Laboratory results
Calcium: 10 mg/dL
Serum creatinine: 1.3 mg/dL
Hemoglobin: 9.8 g/dL
Creatinine clearance: 60 mL/min
Serum-free light chain lambda: 0.2 mg/dL
Serum-free light chain kappa: 24 mg/dL
Kappa:lambda ratio: 120
β2-microglobulin: 4 mg/dL
Fluorescence in situ hybridization: amp 1q21+; t(14:16)
Elranatamab reduced the risk of disease progression or death vs standard care in patients with R/R myeloma after prior anti-CD38 therapy and lenalidomide.
Etentamig, a BCMAxCD3 bispecific antibody, was submitted for potential FDA approval based on the phase 3 CERVINO trial in relapsed/refractory multiple myeloma.
During a live event, Robert Orlowski, MD, PhD, and participants discussed how access barriers, disease tempo, and bridging choices shape CAR T referral for a patient with early relapsed multiple myeloma.