Evidence map›Paper›PMID 33563895›Full record

ArticleBlood cancer journal2021

Mass spectrometry for the evaluation of monoclonal proteins in multiple myeloma and related disorders: an International Myeloma Working Group Mass Spectrometry Committee Report.

David L Murray, Noemi Puig, Sigurdur Kristinsson, Saad Z Usmani, Angela Dispenzieri, Giada Bianchi, Shaji Kumar, Wee Joo Chng, Roman Hajek, Bruno Paiva and 3 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06489613 (Screening for Monoclonal Gammopathy in Individuals Undergoing Physical Examinations Using iMS-LC Assay Technology.), which is not on this map. Cited by 82 papers.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed
16.5field-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.

NCT06489613 unknown statusnot on this mapstarted 2024, after this paper: background citation

Screening for Monoclonal Gammopathy in Individuals Undergoing Physical Examinations Using iMS-LC Assay Technology.

TypeobservationalSponsorJian LiRan2024 to 2025Enrolled15,600ConditionsM Protein, Monoclonal Gammopathy, Monoclonal Gammopathy of Undetermined SignificanceArmsM protein detection by iMS-LC Assay
3 · Its place in the literature

Who cites it

82 citing papers in PubMed, 161 citations in OpenAlex.

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

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

13 authors at 10 institutions in 6 countries.

David L MurrayDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA. murray.david@mayo.edu.ORCID http://orcid.org/0000-0003-1720-335X
Noemi PuigHospital Universitario de Salamanca, Instituto de Investigación Biomédica de Salamanca, Salamanca, Spain.
Sigurdur KristinssonFaculty of Medicine, University of Iceland, Reykjavík, Iceland.
Saad Z UsmaniDepartment of Hematologic Oncology & Blood Disorders, Levine Cancer Institute/Atrium Health, Charlotte, NC, USA.ORCID http://orcid.org/0000-0002-5484-8731
Angela DispenzieriDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-8780-9512
Giada BianchiDivision of Hematology, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Shaji KumarDepartment of Hematology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0001-5392-9284
Wee Joo ChngCancer Science Institute of Singapore, NUS, Singapore, Singapore.
Roman HajekDepartment of Hematooncology, University Hospital Ostrava and Faculty of Medicine, University of Ostrava, Ostrava, Czech Republic.ORCID http://orcid.org/0000-0001-6955-6267
Bruno PaivaClinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), IDISNA, Pamplona, Spain.ORCID http://orcid.org/0000-0003-1977-3815
Anders WaageDepartment of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
S Vincent RajkumarDepartment of Hematology, Mayo Clinic, Rochester, MN, USA.ORCID http://orcid.org/0000-0002-5862-1833
Brian DurieDepartment of Hematology, Cedars-Sinai Outpatient Cancer Center, Los Angeles, CA, USA.
Mayo Clinic in Arizona · USBrigham and Women's Hospital · USCedars-Sinai Medical Center · USClinica Universidad de Navarra · ESInstituto de Investigación Biomédica de Salamanca · ESLevine Cancer Institute · USNational University Cancer Institute, Singapore · SGNorwegian University of Science and Technology · NOUniversity of Iceland · ISUniversity of Ostrava · CZ

Funding

Project 4: Targeting Resistance to T-Cell Directed Therapy in Multiple MyelomaP50CA186781 · NCI · MAYO CLINIC ARIZONA · PI Rafael Fonseca · 2015 to 2026
$25.5M
Onset and biomarkers for progression of monoclonal gammopathiesR01CA168762 · NCI · MAYO CLINIC ROCHESTER · PI KUMAR, SHAJI KUNNATHU, RAJKUMAR, S VINCENT · 2012 to 2024
$3.2M
NCI NIH HHS P50 CA186781NCI NIH HHS R01 CA168762
6 · The paper itself

Abstract

Plasma cell disorders (PCDs) are identified in the clinical lab by detecting the monoclonal immunoglobulin (M-protein) which they produce. Traditionally, serum protein electrophoresis methods have been utilized to detect and isotype M-proteins. Increasing demands to detect low-level disease and new therapeutic monoclonal immunoglobulin treatments have stretched the electrophoretic methods to their analytical limits. Newer techniques based on mass spectrometry (MS) are emerging which have improved clinical and analytical performance. MS is gaining traction into clinical laboratories, and has replaced immunofixation electrophoresis (IFE) in routine practice at one institution. The International Myeloma Working Group (IMWG) Mass Spectrometry Committee reviewed the literature in order to summarize current data and to make recommendations regarding the role of mass spectrometric methods in diagnosing and monitoring patients with myeloma and related disorders. Current literature demonstrates that immune-enrichment of immunoglobulins coupled to intact light chain MALDI-TOF MS has clinical characteristics equivalent in performance to IFE with added benefits of detecting additional risk factors for PCDs, differentiating M-protein from therapeutic antibodies, and is a suitable replacement for IFE for diagnosing and monitoring multiple myeloma and related PCDs. In this paper we discuss the IMWG recommendations for the use of MS in PCDs.

Indexed as

Chromatography, LiquidHumansImmunoglobulin Light ChainsMultiple MyelomaMyeloma ProteinsNeoplasms, Plasma CellSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationImmunoglobulin Light Chainsmultiple myeloma M-proteinsMyeloma Proteins

Identifiers

PMID33563895
PMCPMC7873248
OpenAlexW3128280352

What OpenQuestion holds

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LicenceCC BY
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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.