Evidence map›Paper›PMID 42456135›Full record

Trial reportThe New England journal of medicine2026

Continuous or Fixed-Duration Maintenance Therapy in Multiple Myeloma.

Shaji Kumar, Susanna Jacobus, Adam Cohen, Matthias Weiss, Natalie Callander, Avina Singh, Terri Parker, Michael Green, Raymond Thertulien, Benjamin Parsons and 14 more

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

Trial report in The New England journal of medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01863550 (Randomized Phase III Trial of Bortezomib, Lenalidomide, and Dexamethasone), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT01863550 phase3active not recruitingnot on this map

Randomized Phase III Trial of Bortezomib, Lenalidomide, and Dexamethasone (VRd) Versus Carfilzomib, Lenalidomide, and Dexamethasone (CRd) Followed by Limited or Indefinite Duration Lenalidomide Maintenance in Patients With Newly Diagnosed Symptomatic Multiple Myeloma (ENDURANCE)

TypeinterventionalSponsorECOG-ACRIN Cancer Research GroupRan2013 to 2034Enrolled1,087ConditionsPlasma Cell MyelomaArmsBortezomib, Carfilzomib, Dexamethasone, Laboratory Biomarker Analysis, Lenalidomide
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Review
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

24 authors.

Shaji KumarMayo Clinic, Rochester, MN.ORCID 0000-0001-5392-9284
Susanna JacobusECOG-ACRIN Biostatistics Center, Boston.
Adam CohenUniversity of Pennsylvania, Philadelphia.
Matthias WeissThedaCare Regional Medical Center, Appleton, WI.
Natalie CallanderUniversity of Wisconsin, Madison.
Avina SinghFairview Ridges Hospital, Burnsville, MN.
Terri ParkerYale University School of Medicine, New Haven, CT.
Michael GreenKaiser Permanente, Oakland, CA.
Raymond ThertulienNovant Heath, Charlotte, NC.
Benjamin ParsonsGundersen Lutheran Medical Center, La Crosse, WI.
Pankaj KumarIllinois CancerCare, Bloomington.
Prashant KapoorMayo Clinic, Rochester, MN.
Aaron RosenbergUniversity of California Davis Comprehensive Cancer Center, Sacramento.ORCID 0000-0003-0714-734X
Elie DibTrinity Health, Ann Arbor Campus, Ypsilanti, MI.
Daniel AlmquistSanford Roger Maris Cancer Center, Fargo, ND.
Jeffrey ZonderBarbara Ann Karmanos Cancer Institute, Wayne State University, Detroit.
Edward FaberDayton Clinical Oncology Program, Dayton, OH.
Zihan WeiECOG-ACRIN Biostatistics Center, Boston.
Kenneth AndersonDana-Farber Cancer Institute, Boston.
Sagar LonialEmory University, Atlanta.
Paul RichardsonDana-Farber Cancer Institute, Boston.
Robert OrlowskiUniversity of Texas M.D. Anderson Cancer Center, Houston.
Lynne WagnerUniversity of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill.
S Vincent RajkumarMayo Clinic, Rochester, MN.

Funding

ECOG-ACRIN NCORP Research Base - TMISTUG1CA189828 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer, MITCHELL D. SCHNALL · 2014 to 2026
$199.7M
Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
Project-006U10CA180820 · NCI · ECOG-ACRIN MEDICAL RESEARCH FOUNDATION · PI Peter J ODwyer · 2014 to 2026
$167.6M
SWOG Network Group Operations Center of the NCTNU10CA180888 · NCI · UNIVERSITY OF CALIFORNIA AT DAVIS · PI PRIMO N. LARA · 2014 to 2026
$152.1M
Statistics CoreU10CA180794 · NCI · DANA-FARBER CANCER INST · PI PAUL J CATALANO · 2014 to 2026
$111.2M
Kaiser Permanente NCI National Community Oncology Research Program, NCORPUG1CA189821 · NCI · KAISER FOUNDATION RESEARCH INSTITUTE · PI Jennifer Marie Suga · 2014 to 2026
$44.4M
Metro-Minnesota Community Oncology Research Consortium (MMCORC)UG1CA189863 · NCI · PARK NICOLLET INSTITUTE · PI JOLEEN M HUBBARD, Yan Ji · 2014 to 2026
$43.2M
Heartland Cancer Research NCORPUG1CA189830 · NCI · DECATUR MEMORIAL HOSPITAL · PI Bryan A. Faller · 2014 to 2026
$40.9M
Southeast Clinical Oncology Research Consortium, Inc. (SCOR)UG1CA189858 · NCI · SOUTHEAST CLINICAL ONCOL RES CONSORTIUM · PI Judith O Hopkins, William J Irvin · 2014 to 2026
$38.8M
Michigan Cancer Research Consortium NCORPUG1CA189971 · NCI · SAINT JOSEPH MERCY HEALTH SYSTEM · PI Tareq Al baghdadi · 2014 to 2026
$36.6M
Wisconsin NCI Community Oncology Research Program (WiNCORP)UG1CA189956 · NCI · MARSHFIELD CLINIC RESEARCH FOUNDATION · PI ADEDAYO A ONITILO, Kurt Oettel · 2014 to 2026
$32.3M
Sanford Community Cancer Program of the North Central Plains (NCORP)UG1CA189825 · NCI · SANFORD RESEARCH/USD · PI Daniel Almquist, SAMUEL J. MILANOVICH · 2014 to 2026
$13.6M
NCI NIH HHS U10 CA180794NCI NIH HHS U10 CA180820NCI NIH HHS U10CA180820, U10CA180794, UG1CA189828, UG1CA232760NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180888NCI NIH HHS UG1 CA189821NCI NIH HHS UG1 CA189825NCI NIH HHS UG1 CA189828NCI NIH HHS UG1 CA189830NCI NIH HHS UG1 CA189858NCI NIH HHS UG1 CA189863NCI NIH HHS UG1 CA189956NCI NIH HHS UG1 CA189957NCI NIH HHS UG1 CA189971NCI NIH HHS UG1 CA232760NCI NIH HHS UG1 CA233163NCI NIH HHS UG1 CA233180NCI NIH HHS UG1 CA233247NCI NIH HHS UG1 CA233277NCI NIH HHS UG1 CA233329NCI NIH HHS UG1 CA233337NCI NIH HHS UG1 CA233340
6 · The paper itself

Abstract

backgroundCurrent treatment of newly diagnosed multiple myeloma involves lenalidomide maintenance therapy given until disease progression. The appropriate duration of maintenance therapy with lenalidomide has been unclear.

methodsIn this phase 3 trial, we enrolled patients with standard-risk newly diagnosed multiple myeloma who were not undergoing up-front autologous stem-cell transplantation. After induction treatment with a proteasome inhibitor-lenalidomide combination, patients were randomly assigned to receive indefinite-duration (continuous) lenalidomide or fixed-duration lenalidomide (for 2 years). The primary end point was overall survival; the trial had 80% power to detect a 50% increase in median survival (from 5 years to 7.5 years), with a two-sided alpha level of 5%, 395 patients undergoing randomization, and 204 deaths occurring during 9 years of follow-up.

resultsAt the end of induction, 516 patients were randomly assigned to the indefinite-duration group (260 patients) or the fixed-duration group (256 patients). At a median follow-up of 86 months, overall survival did not differ significantly between the groups. With 80 deaths in each group, overall survival at 7 years was 68.6% in the indefinite-duration group and 69.0% in the fixed-duration group (difference, -0.4 percentage points; 95 confidence interval [CI], -9.0 to 8.3; P = 0.93). Progression-free survival at 7 years was 36.1% in the indefinite-duration group and 29.7% in the fixed-duration group (difference, 6.4 percentage points; 95% CI, -2.6 to 15.4). The 5-year cumulative incidence of second primary cancers, excluding nonmelanoma skin cancer, was 11.2% with indefinite-duration lenalidomide and 8.3% with fixed-duration lenalidomide. More adverse events occurred with indefinite-duration lenalidomide; the incidence of nonhematologic events of grade 3 or higher was 48.2% with indefinite-duration therapy and 31.5% with fixed-duration therapy.

conclusionsIn this phase 3 trial involving patients with standard-risk newly diagnosed multiple myeloma who were not undergoing up-front autologous stem-cell transplantation, indefinite-duration maintenance therapy after induction therapy did not result in significantly longer overall survival than fixed-duration maintenance therapy. (Funded by the National Cancer Institute of the National Institutes of Health and Amgen; ENDURANCE ClinicalTrials.gov number, NCT01863550.).

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLenalidomideMaintenance ChemotherapyMultiple MyelomaNeoplasms, Second PrimaryAdultAgedBortezomibDexamethasoneDisease ProgressionDrug Administration ScheduleFemaleFollow-Up StudiesHumansIncidenceKaplan-Meier EstimateBortezomibcarfilzomibDexamethasoneLenalidomideOligopeptidesProteasome Inhibitors

Identifiers

PMID42456135
PMCPMC13374710

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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.