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)
During a live event, Sikander Ailawadhi, MD, and participants considered a case patient with relapsed multiple myeloma after a quadruplet induction who declined CAR T-cell therapy.
The UK's OPTIMUM trial showed significant differences with a more aggressive treatment regimen for high-risk newly diagnosed multiple myeloma, based on long-term follow-up.
During a live Case-Based Roundtable event, Brea Lipe, MD, and participants discussed treatment options for an older patient who already received multiple bispecific antibodies for multiple myeloma.