About this trial
This is a prospective, single-center, clinical study to evaluate the efficacy and safety of a fully immunotherapy-based strategy guided by MRD-driven dynamic risk stratification in transplant-ineligible patients with newly diagnosed multiple myeloma.
Eligibility criteria
Qualifiers
Age ≥ 18 years and ≤ 75 years.
Participants with documented newly-diagnosed multiple myeloma according to IMWG diagnostic criteria.
Measurable disease at screening, defined as: Serum M-protein level ≥1.0 g/dL or urine M-protein level ≥200 mg/24 hours; or Light chain MM without measurable disease in serum or urine: serum Ig free-light chain (FLC) ≥10 mg/dL and abnormal serum Ig kappa lambda FLC ratio.
Patients deemed ineligible for high-dose chemotherapy with ASCT due to any of the following: Age ≥65 years; Investigator assessment of ineligibility; ECOG performance status 3-4; Repeated failure of hematopoietic stem cell mobilization; Patient's decision to defer ASCT.
Disqualifiers
Active amyloidosis.
Central nervous system involvement.
Prior BCMA-targeted therapy or CAR-T therapy.
Active hepatitis B or hepatitis C virus infection.
Trial design
Treatments tested in this trial
- BCMA CAR-T
- GPRC5D/CD3 BiTEs