Is SARCLISA + Pd appropriate for your RRMM patients?

Meet John — A patient with relapsed and refractory MM with high risk cytogenetics* and disease progression after 3L treatment

74 years old
Time since MM diagnosis
3 years
R-ISS stage at diagnosis
Stage III
Additional medical history

Initial treatment

  • John was ineligible for ASCT and treatment was initiated with the cyclophosphamide, thalidomide, dexamethasone (CTd) regimen
  • Cytogenetic analysis showed translocation t(4:14)

Disease progression

  • John’s disease progressed after 1.5 years
  • John received second-line treatment with the bortezomib, dexamethasone (Vd) regimen and achieved a VGPR
  • One year later, John was diagnosed with disease progression after a regular follow-up with his doctor and received ixazomib, lenalidomide, dexamethasone (IxaRd) and achieved a partial response (PR)
  • John had disease progression while on therapy with IxaRd

Additional patient information

Cytogenetic risk
Bone marrow plasma cells
11 g/dL
Multiple bone lesions
Beta-2 microglobulin
4.0 µL/mL
Renal function (CrCl)
80 mL/min/1.73 m2
Would John be a candidate for treatment with SARCLISA + Pd?

John would be eligible for treatment with SARCLISA + Pd1,2

Percentage of patients receiving SARCLISA + Pd in the ICARIA-MM trial with similar baseline characteristics2

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