PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
May 29, 2026Journal of Clinical Oncology1 citations

DREAMM-9 final analysis: Belantamab mafodotin (belamaf), bortezomib, lenalidomide, and dexamethasone (BVRd) for transplant-ineligible (TI) newly diagnosed multiple myeloma (NDMM).

View Full Paper
SUSaad Z. UsmaniMMMichał MielnikAAAránzazu Alonso

Key Points

  • This analysis aims to evaluate the safety and efficacy of BVRd in transplant-ineligible patients with newly diagnosed multiple myeloma.
  • Patients received BVRd across different dosing cohorts: Q3/4W, Q6/8W, Q9/12W, and Q12W.
  • Safety, overall response rates, and patient-reported outcomes were assessed, with a focus on minimal residual disease negativity.
  • Median dose intensities were calculated for both induction and maintenance phases.
  • Overall response rates were ≥83% across all dosing cohorts.
  • Higher induction median dose intensities were associated with deeper responses, showing CR+/MRD[-] rates of 75/55% in pooled SHORT+STRETCH cohorts vs. 59/43% in pooled Q9/12W+Q12W.
  • Grade ≥2 ophthalmic exam findings occurred in 90% for pooled SHORT+STRETCH cohorts, with lower rates of grade 3/4 findings in longer dosing intervals.

Abstract

7503 Background: DREAMM-9 (NCT04091126) was a phase 1 dose and schedule evaluation study of BVRd in adults with TI NDMM. Methods: Patients (pts) received BVRd in 1 of 8 belamaf dosing cohorts at an induction/maintenance schedule of Q3/4W (SHORT: 1.9, 1.4, 1.0 mg/kg), Q6/8W (STRETCH: 1.9, 1.4 mg/kg), Q9/12W (step-down S/D: 1.9 for 1 dose then 1.4 mg/kg; 1.4 for 1 dose then 1.0 mg/kg), or Q12W (1.0 mg/kg). The primary endpoint was safety. Responses, minimal residual disease negativity (MRD-) in complete response or better (CR+), and pt-reported outcomes (PROs) were assessed. Median dose intensities (mDIs) were calculated as mg/kg/21 days in induction and mg/kg/28 days in maintenance. Results: As of June 2, 2025, 118 pts were enrolled (intention-to-treat population). Median duration of follow-up was 15.9–47.1 months. Induction mDI generally decreased as planned dosing intervals increased and was lowest in S/D Q9/12W or Q12W cohorts. Maintenance mDI was similar across cohorts due to dose modifications. Overall response rates were ≥83% across cohorts. Cohorts with higher induction mDI had the deepest responses (CR+/MRD- 75/55% for pooled SHORT+STRETCH and 59/43% for pooled Q9/12W+Q12W). Grade (Gr) ≥2 ophthalmic exam findings (OEFs; best-corrected visual acuity changes/slit lamp findings Keratopathy and Visual Acuity scale) were 90% for pooled SHORT+STRETCH/69% for pooled Q9/12W+Q12W, while Gr 3/4 OEF rates were higher with higher induction mDI (79%/35%). Most cohorts (5/8) had no belamaf discontinuations due to Gr ≥3 OEFs, which occurred only in SHORT cohorts (n = 1 each). First Gr ≥2 OEFs resolved prior to end of treatment in 83–100% across cohorts. The long-interval group (Q9/12W and Q12W dosing schedules) remained largely below the vision-related function (VRF) deterioration threshold (12.5 points per Ocular Surface Disease Index) across most timepoints, suggesting a favorable VRF profile vs the SHORT interval group. Conclusions: BVRd had high response rates across all cohorts (≥83%), highlighting the promising efficacy of the regimen. Regimens with higher belamaf induction mDI had the deepest responses, while those with lower induction mDI had milder OEFs. Belamaf dosing with a higher induction DI is optimal to achieve deeper responses, and a lower maintenance DI (i.e., using longer schedules) improves tolerability, PROs, and maintains responses. Clinical trial information: NCT04091126 .

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Usmani et al. (2026) studied this question.

synapsesocial.com/papers/6a192d7efab5b468c4416654https://doi.org/10.1200/jco.2026.44.16_suppl.7503
Ask AI
Helpful
Bookmark
Share
View Full Paper