Evidence map›Paper›PMID 30249784›Full record

Trial reportBlood2018

Minimal residual disease negativity using deep sequencing is a major prognostic factor in multiple myeloma.

Aurore Perrot, Valerie Lauwers-Cances, Jill Corre, Nelly Robillard, Cyrille Hulin, Marie-Lorraine Chretien, Thomas Dejoie, Sabrina Maheo, Anne-Marie Stoppa, Brigitte Pegourie and 30 more

Registry-linked trialAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06109233 (A Perspective Study of the MRD-tailored Therapy in Patients With Newly Diagnosed Multiple Myeloma With Persistent Minimal Residual Disease After Initial Treatment), which is not on this map. Cited by 225 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
225citing papers in PubMed, 3 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.

NCT06109233 unknown statusnot on this mapstarted 2022, after this paper: background citation

A Perspective Study of the MRD-tailored Therapy in Patients With Newly Diagnosed Multiple Myeloma With Persistent Minimal Residual Disease After Initial Treatment

TypeobservationalSponsorFengYan JinRan2022 to 2026Enrolled80ConditionsMultiple Myeloma, Minimal Residual Disease
3 · Its place in the literature

Who cites it

225 citing papers in PubMed, 3 syntheses or guidelines pooled it.

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165 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

40 authors.

Aurore PerrotHematology Department, University Hospital, Nancy, France.ORCID 0000-0003-0131-8689
Valerie Lauwers-CancesEpidemiology and Statistics Department, University Hospital, Toulouse, France.
Jill CorreMyeloma Genomics Lab University Cancer Institute Toulouse (IUCT)-Oncopole, Cancer Research Center of Toulouse (CRCT), INSERM 1037, Toulouse, France.
Nelly RobillardHematology Laboratory, University Hospital, Nantes, France.
Cyrille HulinHematology Department, University Hospital, Bordeaux, France.
Marie-Lorraine ChretienHematology Department, University Hospital, Dijon, France.
Thomas DejoieBiochemistry Laboratory, University Hospital, Nantes, France.
Sabrina MaheoMyeloma Genomics Lab University Cancer Institute Toulouse (IUCT)-Oncopole, Cancer Research Center of Toulouse (CRCT), INSERM 1037, Toulouse, France.
Anne-Marie StoppaHematology Department, Institut Paoli Calmettes, Marseille, France.
Brigitte PegourieHematology Department, University Hospital, Grenoble, France.
Lionel KarlinHematology Department, University Hospital, Lyon, France.
Laurent GarderetHematology Department, Saint-Antoine University Hospital, Paris, France.
Bertrand ArnulfHematology Department, Saint-Louis University Hospital, Paris, France.
Chantal DoyenHematology Department, Centre Hospitalier Universitaire (CHU) Université Catholique de Louvain (UCL) Namur, Yvoir, Belgium.
Nathalie MeulemanHematology Department, Institut Jules Bordet (ULB), Brussels, Belgium.
Bruno RoyerHematology Department, University Hospital, Amiens, France.
Jean-Richard EveillardHematology Department, University Hospital, Brest, France.
Lotfi BenboubkerHematology Department, University Hospital, Tours, France.
Mamoun DibHematology Department, University Hospital, Angers, France.
Olivier DecauxHematology Department, University Hospital, Rennes, France.
Arnaud JaccardHematology Department, University Hospital, Limoges, France.
Karim BelhadjHematology Department, University Hospital, Creteil, France.
Sabine BrechignacHematology Department, University Hospital, Bobigny, France.
Brigitte KolbHematology Department, University Hospital, Reims, France.
Cecile FohrerHematology Department, University Hospital, Strasbourg, France.
Mohamad MohtyHematology Department, Saint-Antoine University Hospital, Paris, France.
Margaret MacroHematology Department, University Hospital, Caen, France.
Paul G RichardsonHematology Department, Dana-Farber Cancer Institute, Boston, MA.
Victoria CarltonAdaptive Biotechnologies, Seattle, WA.
Martin MoorheadAdaptive Biotechnologies, Seattle, WA.
Tom WillisAdaptive Biotechnologies, Seattle, WA.
Malek FahamAdaptive Biotechnologies, Seattle, WA.
Kenneth C AndersonHematology Department, Dana-Farber Cancer Institute, Boston, MA.
Jean-Luc HarousseauHematology Department, Clinique du Confluent, Nantes, France.
Xavier LeleuHematology Department, University Hospital, Poitiers, France.
Thierry FaconHematology Department, University Hospital, Lille, France.
Philippe MoreauHematology Department, University Hospital, Nantes, France; and.
Michel AttalHematology Department, University Hospital, Toulouse, France.
Hervé Avet-LoiseauMyeloma Genomics Lab University Cancer Institute Toulouse (IUCT)-Oncopole, Cancer Research Center of Toulouse (CRCT), INSERM 1037, Toulouse, France.
Nikhil MunshiHematology Department, Dana-Farber Cancer Institute, Boston, MA.

Funding

Trageting the Multiple Myeloma EpigenomeP50CA100707 · NCI · DANA-FARBER CANCER INSTITUTE · PI ANDERSON, KENNETH C., MUNSHI, NIKHIL C. · 2003 to 2023
$45.0M
NCI NIH HHS P50 CA100707
6 · The paper itself

Abstract

The introduction of novel agents has led to major improvements in clinical outcomes for patients with multiple myeloma. To shorten evaluation times for new treatments, health agencies are currently examining minimal residual disease (MRD) as a surrogate end point in clinical trials. We assessed the prognostic value of MRD, measured during maintenance therapy by next-generation sequencing (NGS). MRD negativity was defined as the absence of tumor plasma cell within 1 000 000 bone marrow cells (<10

Indexed as

High-Throughput Nucleotide SequencingAgedAntineoplastic Combined Chemotherapy ProtocolsBone MarrowBortezomibDexamethasoneDisease-Free SurvivalFemaleFollow-Up StudiesHumansLenalidomideMaintenance ChemotherapyMaleMiddle AgedMultiple MyelomaNeoplasm, ResidualBortezomibDexamethasoneLenalidomide

Identifiers

PMID30249784
PMCPMC6284215

What OpenQuestion holds

Textmetadata
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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.