Evidence map›Paper›PMID 42726291›Full record

Trial reportJournal of managed care & specialty pharmacy2026

Economic advantage of daratumumab, bortezomib, lenalidomide, and dexamethasone vs bortezomib, lenalidomide, and dexamethasone for transplant-ineligible or transplant-deferred newly diagnosed multiple myeloma: A cost-per-responder evaluation.

Santosh Gautam, Laura Morrison, Philippe Thompson-Leduc, Avani Samandur, Brian Macomson, Vipin Khare, Xin Yin, Rohan Medhekar

Abstract readComparative StudyClinical Trial, Phase III
In one paragraph

Trial report in Journal of managed care & specialty pharmacy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Santosh GautamJohnson & Johnson, Horsham, PA.
Laura MorrisonAnalysis Group ULC, Montréal, QC, Canada.
Philippe Thompson-LeducAnalysis Group ULC, Montréal, QC, Canada.
Avani SamandurAnalysis Group, Inc., Menlo Park, CA.
Brian MacomsonJohnson & Johnson, Horsham, PA.
Vipin KhareJohnson & Johnson, Horsham, PA.
Xin YinJohnson & Johnson, Horsham, PA.
Rohan MedhekarJohnson & Johnson, Horsham, PA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the phase III CEPHEUS trial, 8 cycles of daratumumab (D), bortezomib (V), lenalidomide (R), and dexamethasone (d) followed by monthly DRd were associated with a higher rate of minimal residual disease (MRD) negativity compared with VRd followed by Rd among patients with transplant-ineligible/transplant-deferred, newly diagnosed multiple myeloma.

objectiveTo compare the health care costs of patients achieving and sustaining MRD negativity with first-line (1L) DVRd vs VRd.

methodsUsing CEPHEUS trial data, an economic model was developed from a US mixed-payer perspective (80% Medicare, 20% commercial) over a 60-month horizon. Model inputs included drug acquisition and administration costs for 1L and second-line (2L) therapies, medical care costs during 1L and 2L treatment, adverse event management costs, and next-generation sequencing MRD testing costs. Cost per patient negative for MRD was calculated based on the cost per patient treated and the cumulative proportion of patients achieving MRD negativity at 60 months after randomization. Cost per patient achieving sustained MRD negativity was estimated based on the proportion of patients with MRD-negative status on at least 2 occasions that were at least 12 months apart during the 60 months after randomization in CEPHEUS. Costs were reported in 2025 US dollars.

resultsAt 60 months, the total costs per patient negative for MRD were $652,113 lower with DVRd vs VRd, driven by a higher proportion of patients achieving MRD-negative status (DVRd = 60.9%; VRd = 39.4%) and the lower 2L treatment costs per patient with MRD-negative status with DVRd vs VRd (DVRd = $186,371; VRd = $958,840), attributable to the lower proportion of patients progressing to 2L treatment (DVRd = 11.2%; VRd = 33.3%). The cost per patient achieving sustained MRD negativity was $1,964,539 lower with DVRd than VRd, driven by a higher proportion of patients achieving sustained MRD negativity (DVRd = 48.7%; VRd = 26.3%) and the $1,203,376 lower 2L treatment costs per patient in the DVRd cohort (DVRd = $233,060; VRd = $1,436,436).

conclusionsAmong patients with transplant-ineligible or transplant-deferred newly diagnosed multiple myeloma, 1L treatment with DVRd was associated with lower costs per patient with MRD-negative status and per patient achieving sustained MRD negativity compared with treatment with VRd. These findings complement the superior clinical efficacy observed with 1L DVRd compared with VRd in the CEPHEUS trial by demonstrating the potential cost savings associated with DVRd.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsMultiple MyelomaAgedAntibodies, MonoclonalBortezomibCost-Benefit AnalysisDexamethasoneDrug CostsFemaleHealth Care CostsHumansLenalidomideMaleModels, EconomicNeoplasm, ResidualUnited StatesAntibodies, MonoclonalBortezomibdaratumumabDexamethasoneLenalidomide

Identifiers

PMID42726291
PMCPMC13621899

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.