ArticleJournal of managed care & specialty pharmacy2025
Cost-per-responder analysis of daratumumab, bortezomib, lenalidomide, and dexamethasone vs bortezomib, lenalidomide, and dexamethasone among transplant-eligible patients with newly diagnosed multiple myeloma.
Article in Journal of managed care & specialty pharmacy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundThe phase 3 PERSEUS trial demonstrated superior efficacy of daratumumab (D), bortezomib (V), lenalidomide (R), and dexamethasone (d) induction/consolidation followed by DR maintenance (DVRd/DR) vs VRd induction/consolidation followed by R maintenance (VRd/R) in transplant-eligible patients with newly diagnosed multiple myeloma.
objectiveTo assess the economic value associated with achieving and sustaining minimal residual disease (MRD)-negative status with DVRd/DR vs VRd/R.
methodsA model of cost per patient with MRD-negative status was developed from a US mixed-payer perspective (60% Medicare, 40% commercial) using PERSEUS trial data. Model inputs included costs for first-line (1L) and second-line (2L) treatment, autologous stem cell transplant, medical care, adverse event management, and MRD testing. Outcomes included the cost per MRD-negative patient, calculated using the cost per treated patient and cumulative proportion of patients achieving MRD-negative status at 48 months after randomization, and cost per patient sustaining MRD negativity for at least 12 months during maintenance, calculated using maintenance treatment costs and the proportion of patients who converted from MRD-positive at the end of consolidation to achieving sustained MRD-negative status during maintenance. Costs were reported in 2025 US dollars.
resultsAt 48 months, the total cost per patient with MRD-negative status was lower with DVRd/DR compared with VRd/R ($519,999 less). Key drivers of these cost savings included the lower maintenance treatment costs per MRD-negative patient ($106,707 less) and the lower 2L treatment costs per MRD-negative patient ($434,184 less) with DVRd/DR compared with VRd/R. The lower maintenance treatment costs with DVRd/DR were attributable to the higher proportion of patients achieving MRD-negative status. The lower 2L treatment costs with DVRd/DR were attributable to the lower proportion of patients initiating 2L (9.4%) compared with VRd/R (26.8%). Among patients who were MRD-positive at the end of consolidation, the cost per patient achieving sustained MRD-negative status was lower with DVRd/DR vs VRd/R, resulting in savings of $961,880. This was primarily attributable to a higher proportion of patients achieving sustained MRD-negative status with DVRd/DR (44.2%) than with VRd/R (22.6%) during the maintenance phase.
conclusionsThe cost per MRD-negative patient and the cost per patient achieving sustained MRD negativity during maintenance were lower with DVRd/DR compared with VRd/R. These findings demonstrate the cost savings associated with the use of DVRd induction/consolidation followed by DR maintenance for transplant-eligible patients with newly diagnosed multiple myeloma, supplementing the superior efficacy benefits relative to VRd induction/consolidation demonstrated in the PERSEUS trial.
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