Suzanne Lentzsch, MD, discusses data from the following study:
- The INSURE study (INSIGHT MM, UVEA-IXA, REMIX): a pooled analysis of relapsed/refractory multiple myeloma (RRMM) patients (pts) treated with
ixazomib-lenalidomide-dexamethasone (IRd) in routine clinical practice. (Leleu X et al. Blood. 2021;138[suppl 1]:2701).- Ixazomib in combination with lenalidomide and dexamethasone has been approved for the treatment of RRMM based on the results of the TOURMALINE-MM1 phase 3 study. However, outcomes in routine clinical practice often differ from data reported in clinical trials for MM therapies, being poorer for real-world versus clinical trial patients.
- Several retrospective and prospective observational studies have shown comparable effectiveness of IRd in the second and later lines of therapy (LoTs) in the real-world setting with the efficacy observed in TOURMALINE-MM1, with median progression-free survival (PFS) ranging from 11 months to 43 months. The objective of the current analysis of a large, global dataset pooled from 3 observational studies is to investigate the effectiveness of IRd in the overall RRMM population, by LoT, and in subpopulations of patients defined by frailty status.
- In all, 564 adults with RRMM from several clinical trials (INSIGHT, UVEA-IXA, and REMIX) were included in a pooled analysis. Primary outcome measures were time to next therapy and PFS. Secondary outcome measures included duration of therapy, overall survival, overall response rate (ORR), and safety.
- Results/Conclusions:
- The effectiveness of IRd in routine clinical practice (median PFS, 19.9 months; ORR, 65%) is consistent with the efficacy of IRd observed in the registrational TOURMALINE-MM1 trial (median PFS, 20.6 months; ORR, 78%), with no new safety concerns reported.
- A very good partial response was noted among 17% of frail patients vs 42% of nonfrail patients.
- The ORR was 70% in the 2nd LoT, 63% in the 3rd LoT, and 53% in the 4th LoT.