Evidence map›Paper›PMID 39331724›Full record

Trial reportBlood2025

Daratumumab with lenalidomide as maintenance after transplant in newly diagnosed multiple myeloma: the AURIGA study.

Ashraf Badros, Laahn Foster, Larry D Anderson, Chakra P Chaulagain, Erin Pettijohn, Andrew J Cowan, Caitlin Costello, Sarah Larson, Douglas W Sborov, Kenneth H Shain and 11 more

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Blood, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03901963 (A Randomized Study of Daratumumab Plus Lenalidomide Versus Lenalidomide Alone as Maintenance Treatment in Patients With Newly Diagnosed Multiple Myeloma Who Are Minimal Residual Disease Positive After Frontline Autologous Stem Cell Transplant), which is not on this map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
–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.

NCT03901963 phase3completednot on this map

A Randomized Study of Daratumumab Plus Lenalidomide Versus Lenalidomide Alone as Maintenance Treatment in Patients With Newly Diagnosed Multiple Myeloma Who Are Minimal Residual Disease Positive After Frontline Autologous Stem Cell Transplant

TypeinterventionalSponsorJanssen Research & Development, LLCRan2019 to 2026Enrolled200ConditionsMultiple MyelomaArmsDaratumumab, Lenalidomide
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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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

21 authors.

Ashraf BadrosGreenebaum Comprehensive Cancer Center, University of Maryland, Baltimore, MD.ORCID 0000-0003-1690-0188
Laahn FosterDivision of Hematology and Oncology, University of Virginia, Charlottesville, VA.
Larry D AndersonDivision of Hematology and Oncology, Myeloma, Waldenstrom's and Amyloidosis Program, Simmons Comprehensive Cancer Center, The University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-6531-9595
Chakra P ChaulagainMyeloma and Amyloidosis Program, Department of Hematology and Oncology, Cleveland Clinic Florida, Weston, FL.ORCID 0000-0002-4641-2217
Erin PettijohnThe Cancer and Hematology Centers of Western Michigan, Grand Rapids, MI.
Andrew J CowanDivision of Medical Oncology, Fred Hutchinson Cancer Center, University of Washington, Seattle, WA.
Caitlin CostelloMoores Cancer Center, University of California San Diego, La Jolla, CA.
Sarah LarsonDivision of Hematology and Oncology, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA.
Douglas W SborovDepartment of Internal Medicine-Division of Hematology and Hematologic Malignancies, Huntsman Cancer Institute, The University of Utah, Salt Lake City, UT.ORCID 0000-0003-4268-2698
Kenneth H ShainDepartment of Malignant Hematology, H. Lee Moffitt Cancer Center, Tampa, FL.ORCID 0000-0003-4178-8888
Rebecca SilbermannDivision of Hematology/Medical Oncology, Knight Cancer Institute, Oregon Health and Science University, Portland, OR.
Nina ShahDepartment of Medicine, University of California San Francisco, San Francisco, CA.
Alfred ChungDepartment of Medicine, University of California San Francisco, San Francisco, CA.ORCID 0000-0003-0196-5456
Maria KrevvataJanssen Research and Development, LLC, Spring House, PA.
Huiling PeiJanssen Research and Development, LLC, Titusville, NJ.
Sharmila PatelJanssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA.
Vipin KhareJanssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA.ORCID 0000-0003-2875-1079
Annelore CortoosJanssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA.
Robin CarsonJanssen Research and Development, LLC, Spring House, PA.
Thomas S LinJanssen Scientific Affairs, LLC, a Johnson & Johnson company, Horsham, PA.
Peter VoorheesDepartment of Hematologic Oncology and Blood Disorders, Levine Cancer Institute, Atrium Health Wake Forest University School of Medicine, Charlotte, NC.ORCID 0000-0003-1661-718X

Funding

UT Southwestern Medical Center Simmons Comprehensive Cancer CenterP30CA142543 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI MELANIE H. COBB · 2010 to 2026
$53.7M
NCI NIH HHS P30 CA142543
6 · The paper itself

Abstract

abstractNo randomized trial has directly compared daratumumab and lenalidomide (D-R) maintenance with standard-of-care lenalidomide (R) alone after transplant. Herein, we report the primary results of the phase 3 AURIGA study evaluating D-R vs R maintenance in patients with newly diagnosed multiple myeloma (NDMM) who had very good or better partial response, were minimal residual disease (MRD)-positive (10-5) and anti-CD38-naïve after transplant. Two hundred patients were randomly assigned (1:1) to D-R (n = 99) or R (n = 101) maintenance for up to 36 cycles. The MRD-negative (10-5) conversion rate by 12 months from start of maintenance (primary end point) was significantly higher for D-R than R (50.5% vs 18.8%; odds ratio [OR], 4.51; 95% confidence interval [CI], 2.37-8.57; P < .0001). MRD-negative (10-6) conversion rate was similarly higher with D-R (23.2% vs 5.0%; OR, 5.97; 95% CI, 2.15-16.58; P = .0002). At median follow-up (32.3 months), D-R achieved a higher overall MRD-negative (10-5) conversion rate (D-R, 60.6% vs R, 27.7%; OR, 4.12; 95% CI, 2.26-7.52; P < .0001) and complete response rate or better (75.8% vs 61.4%; OR, 2.00; 95% CI, 1.08-3.69; P = .0255) vs R. Progression-free survival (PFS) favored D-R vs R (hazard ratio, 0.53; 95% CI, 0.29-0.97); estimated 30-month PFS rates were 82.7% for D-R and 66.4% for R. Incidences of grade 3/4 cytopenias (54.2% vs 46.9%) and infections (18.8% vs 13.3%) were slightly higher with D-R than R. In conclusion, D-R maintenance achieved a higher MRD-negative conversion rate and improved PFS after transplant vs R, with no new safety concerns. This trial was registered at www.clinicaltrials.gov as #NCT03901963.

Indexed as

Antibodies, MonoclonalAntineoplastic Combined Chemotherapy ProtocolsHematopoietic Stem Cell TransplantationLenalidomideMultiple MyelomaAdultAgedFemaleHumansMaintenance ChemotherapyMaleMiddle AgedNeoplasm, ResidualAntibodies, MonoclonaldaratumumabLenalidomide

Identifiers

PMID39331724
PMCPMC11775507

What OpenQuestion holds

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Registered trials

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 OpenQuestion graph.