Evidence map›Paper›PMID 27632282›Full record

SynthesisJAMA oncology2017

Association of Minimal Residual Disease With Superior Survival Outcomes in Patients With Multiple Myeloma: A Meta-analysis.

Nikhil C Munshi, Herve Avet-Loiseau, Andy C Rawstron, Roger G Owen, J Anthony Child, Anjan Thakurta, Paul Sherrington, Mehmet Kemal Samur, Anna Georgieva, Kenneth C Anderson and 1 more

4 registry-linked trialsOpen access · bronzeAbstract readMeta-Analysis
In one paragraph

Synthesis in JAMA oncology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 289 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
289citing papers in PubMed, 7 pooled it
30.9field-weighted citation impact, top 1% of its field
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.

NCT04943302 phase2withdrawnnot on this mapstarted 2022, after this paper: background citation

Isatuximab and Bendamustine in Systemic Light Chain Amyloidosis

TypeinterventionalSponsorTufts Medical CenterRan2022 to 2026Enrolled0ConditionsAmyloidosis, Light Chain (AL) AmyloidosisArmsBendamustine Hydrochloride, Isatuximab
NCT05378971 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Clinical Research of Pomalidomide Maintenance Therapy for Primary Multiple Myeloma

TypeinterventionalSponsorLanZhou UniversityRan2022 to 2025Enrolled15ConditionsMultiple MyelomaArmsPomalidomide
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
NCT06282978 phase2active not recruitingnot on this mapstarted 2023, after this paper: background citation

An Open Label, Multicenter, Phase II Study of Elranatamab as Single Agent for the Treatment of Relapsed or Refractory Myeloma in Patients Previously Exposed to Three-drug Classes (GEM-RANTAB)

TypeinterventionalSponsorPETHEMA FoundationRan2023 to 2029Enrolled50ConditionsMultiple Myeloma in RelapseArmsElranatamab (PF-06863135)
3 · Its place in the literature

Who cites it

289 citing papers in PubMed, 7 syntheses or guidelines pooled it, 515 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 4 countries.

Nikhil C MunshiDana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Herve Avet-LoiseauUnit for Genomics in Myeloma, Institut Universitaire du Cancer, Toulouse, France.
Andy C RawstronSt James's University Hospital, Leeds, United Kingdom.
Roger G OwenSt James's University Hospital, Leeds, United Kingdom.
J Anthony ChildUniversity of Leeds, Leeds, United Kingdom.
Anjan ThakurtaCelgene Corporation, Summit, New Jersey.
Paul SherringtonCelgene International, Boudry, Switzerland.
Mehmet Kemal SamurDana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Anna GeorgievaExcerpta Medica, Amsterdam, the Netherlands.
Kenneth C AndersonDana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts.
Walter M GregoryUniversity of Leeds, Leeds, United Kingdom.
Dana-Farber Cancer Institute · USSt James's University Hospital · GBUniversity of Leeds · GBBristol-Myers Squibb (Switzerland) · CHHarvard University · USInstitut universitaire du cancer de Toulouse Oncopole · FR

Funding

Targeting Genomic Instability and Evolution in MyelomaP01CA155258 · NCI · DANA-FARBER CANCER INST · PI Jill Corre · 2011 to 2026
$32.5M
Medical Research Council G0100132NCI NIH HHS P01 CA155258
6 · The paper itself

Abstract

importanceNumerous studies have evaluated the prognostic value of minimal residual disease (MRD) in patients with multiple myeloma (MM). Most studies were small and varied in terms of patient population, treatment, and MRD assessment methods.

objectiveTo evaluate the utility of MRD detection in patients with newly diagnosed MM. DATA SOURCES: A Medline search was conducted for articles published in English between January 1990 and January 2016. STUDY SELECTION: Eligible studies reported MRD status and progression-free survival (PFS) or overall survival (OS) in 20 or more patients following treatment. Among 405 articles identified, 21 met the initial eligibility criteria and were included in the analysis. DATA EXTRACTION AND SYNTHESIS: Information on patient characteristics, treatment, MRD assessment, and outcomes were extracted using a standard form. MAIN OUTCOMES AND MEASURES: The impact of MRD status on PFS and OS was assessed by pooling data from relevant trials. Data were adjusted to allow for different proportions of patients with MRD in different studies, and analyzed using the Peto method. Forest plots were created based on Cox model analysis. Other prespecified research questions were addressed qualitatively.

resultsFourteen studies (n = 1273) provided data on the impact of MRD on PFS, and 12 studies (n = 1100) on OS. Results were reported specifically in patients who had achieved conventional complete response (CR) in 5 studies for PFS (n = 574) and 6 studies for OS (n = 616). An MRD-negative status was associated with significantly better PFS overall (hazard ratio [HR], 0.41; 95% CI, 0.36-0.48; P < .001) and in studies specifically looking at CR patients (HR, 0.44; 95% CI, 0.34-0.56; P < .001). Overall survival was also favorable in MRD-negative patients overall (HR, 0.57; 95% CI, 0.46-0.71; P < .001) and in CR patients (HR, 0.47; 95% CI, 0.33-0.67; P < .001). Tests of heterogeneity found no significant differences among the studies for PFS and OS. CONCLUSIONS AND RELEVANCE: Minimal residual disease-negative status after treatment for newly diagnosed MM is associated with long-term survival. These findings provide quantitative evidence to support the integration of MRD assessment as an end point in clinical trials of MM.

Indexed as

BiomarkersClinical Trials as TopicDisease-Free SurvivalFemaleFlow CytometryHumansMaleMultiple MyelomaNeoplasm, ResidualPrognosisRemission InductionTreatment OutcomeBiomarkers

Identifiers

PMID27632282
PMCPMC5943640
OpenAlexW2518827451

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.