Evidence map›Paper›PMID 40459097›Full record

Trial reportThe New England journal of medicine2025

Measurable Residual Disease-Guided Therapy in Newly Diagnosed Myeloma.

Aurore Perrot, Jérôme Lambert, Cyrille Hulin, Andrea Pieragostini, Lionel Karlin, Bertrand Arnulf, Philippe Rey, Laurent Garderet, Margaret Macro, Martine Escoffre-Barbe and 17 more

Abstract readRandomized Controlled TrialClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in The New England journal of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing 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.

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

34 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

27 authors.

Aurore PerrotService Hématologie, Hôpital Universitaire de Toulouse Oncopole, Université de Toulouse, Toulouse, France.ORCID 0000-0003-0131-8689
Jérôme LambertBiostatistics and Medical Information Department, Hôpital St. Louis, Paris.
Cyrille HulinService d'Hématologie, Hôpital Haut Lévêque, Centre Hospitalier Universitaire (CHU) de Bordeaux, Pessac, France.
Andrea PieragostiniService Hématologie, Hôpital Universitaire de Dijon, Dijon, France.
Lionel KarlinService Hématologie, Hôpital Universitaire Lyon Sud, Pierre-Bénite, France.
Bertrand ArnulfHôpital Universitaire St. Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris.
Philippe ReyCentre Léon Bérard, Lyon, France.
Laurent GarderetService Hématologie, Hôpital Universitaire Pitié-Salpêtrière, AP-HP, Paris.
Margaret MacroService Hématologie, Institut Hématologie de Basse Normandie, Hôpital Universitaire de Caen, Caen, France.
Martine Escoffre-BarbeService Hématologie, Hôpital Universitaire de Rennes, Rennes, France.
Julie GayHôpital de Bayonne, Bayonne, France.
Thomas ChalopinService Hématologie, Hôpital Universitaire de Tours, Tours, France.
Romain GounotService Hématologie, Hôpital Henri Mondor, Créteil, France.
Jean-Marc SchianoService Hématologie, Institut Paoli-Calmettes, Marseille, France.
Mohamad MohtyService Hématologie, Hôpital Universitaire St. Antoine, AP-HP, Université Sorbonne, Paris.ORCID 0000-0002-7264-808X
Xavier LeleuService Hématologie, Hôpital Universitaire de Poitiers, Poitiers, France.
Salomon ManierService Hématologie, Hôpital Universitaire de Lille, Lille, France.
Clara MarietteService Hématologie, Hôpital CHU de Grenoble, Grenoble, France.
Carine ChaleteixService Hématologie, Hôpital Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.
Thorsten BraunService Hématologie, Hôpital Avicenne, AP-HP, Paris.
Bernard De PrijckService Hématologie, Hôpital Universitaire de Liège, Liège, Belgium.
Hervé Avet-LoiseauUnité Génomique du Myélome, Hôpital Universitaire de Toulouse Oncopole, Université de Toulouse, Toulouse, France.
Jean-Yves MaryBiostatistics and Medical Information Department, Hôpital St. Louis, Paris.
Jill CorreUnité Génomique du Myélome, Hôpital Universitaire de Toulouse Oncopole, Université de Toulouse, Toulouse, France.
Philippe MoreauService Hématologie, Hôpital Universitaire de Nantes, Université de Nantes, Nantes, France.
Cyrille TouzeauService Hématologie, Hôpital Universitaire de Nantes, Université de Nantes, Nantes, France.
MIDAS Study Group

Funding

Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Nikhil C. Munshi · 2011 to 2026
$32.5M
NCI NIH HHS P01 CA155258
6 · The paper itself

Abstract

backgroundMeasurable residual disease (MRD) is a major prognostic factor in newly diagnosed multiple myeloma. An assessment of an MRD-guided consolidation strategy in patients who are eligible for autologous stem-cell transplantation (ASCT) may be useful.

methodsIn this phase 3 trial, we randomly assigned transplantation-eligible patients with newly diagnosed myeloma who had completed induction therapy with isatuximab, carfilzomib, lenalidomide, and dexamethasone (Isa-KRd) to receive consolidation therapy according to their MRD status. Patients who were MRD-negative at 10

resultsAmong 485 patients who were MRD-negative at 10

conclusionsAmong patients who were MRD-negative at 10

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsConsolidation ChemotherapyHematopoietic Stem Cell TransplantationMultiple MyelomaAdultAgedAntibodies, Monoclonal, HumanizedDexamethasoneFemaleHumansInduction ChemotherapyLenalidomideMaleMiddle AgedNeoplasm, ResidualOligopeptidesAntibodies, Monoclonal, HumanizedcarfilzomibDexamethasoneisatuximabLenalidomideOligopeptides

Identifiers

PMID40459097
PMCPMC13292240

What OpenQuestion holds

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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 OpenQuestion graph.