Evidence map›Paper›PMID 35157768›Full record

Trial reportBlood advances2022

Mass spectrometry vs immunofixation for treatment monitoring in multiple myeloma.

Noemí Puig, María-Teresa Contreras, Cristina Agulló, Joaquín Martínez-López, Albert Oriol, María-Jesús Blanchard, Rafael Ríos, Jesús Martín, María-Belén Iñigo, Anna Sureda and 15 more

Registry-linked trialOpen access · goldAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01916252 (A Randomized, National, Open-label, Multicenter, Phase III Trial Studying Induction Therapy With Bortezomib/Lenalidomide/Dexamethasone), which is not on this map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
7.2field-weighted citation impact, top 2% 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.

NCT01916252 phase3completednot on this map

A Randomized, National, Open-label, Multicenter, Phase III Trial Studying Induction Therapy With Bortezomib/Lenalidomide/Dexamethasone (VRD-GEM), Followed by High-dose Chemotherapy With Melphalan-200 (MEL-200) Versus Busulfan-melphalan (BUMEL), and Consolidation With VRD-GEM in Patients Under 65 Years Old With Newly-diagnosed, Symptomatic Multiple Myeloma

TypeinterventionalSponsorPETHEMA FoundationRan2013 to 2016Enrolled460ConditionsMultiple MyelomaArmsbortezomib (Velcade ®), lenalidomide (Revlimid®), busulfan (Busilvex ®), Dexamethasone acetate, Melphalan
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  6. Article
  7. Review
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  14. Mass spectrometry in clinical protein laboratories.Advances in laboratory medicine · 2024
    Article
  15. Advances in laboratory medicine · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Monitoring Minimal Residual Disease in Patients with Multiple Myeloma by Targeted Tracking Serum M-Protein Using Mass Spectrometry (EasyM).Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  20. 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

25 authors at 16 institutions in 1 country.

Noemí PuigHematology Department, IBSAL, Instituto de Biología Molecular y Celular del Cáncer-Consejo Superior de Investigaciones Científicas (IBMCC-CSIC), Centro de Investigación Biomédica en Red de Cáncer (CIBERONC).
María-Teresa ContrerasClinical Biochemistry Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Cristina AgullóClinical Biochemistry Department, Hospital Universitario de Salamanca, Salamanca, Spain.
Joaquín Martínez-LópezHospital Universitario 12 de Octubre, Complutense University, i+12, CNIO, CIBERONC CB16/12/00369, Madrid, Spain.ORCID 0000-0001-7908-0063
Albert OriolInstitut Català d'Oncologia, Institut Josep Carreras Hospital Germans i Trials, Barcelona, Spain.ORCID 0000-0001-6804-2221
María-Jesús BlanchardHematology Department, Hospital Ramón y Cajal, Madrid, Spain.
Rafael RíosHematology Department, Hospital Universitario Virgen de las Nieves, Ibs. GRANADA, CIBERESP, Granada, Spain.ORCID 0000-0001-8193-1402
Jesús MartínHospital Universitario Virgen del Rocío, Sevilla, Spain.
María-Belén IñigoHospital Clínico San Carlos, Madrid, Spain.
Anna SuredaInstitut Catalá d'Oncologia-l'Hospitalet, IDIBELL, Universitat de Barcelona, Barcelona, Spain.
Miguel-Teodoro HernándezHospital Universitario de Canarias, Santa Cruz de Tenerife, Spain.ORCID 0000-0002-6576-7881
Javier de la RubiaDepartment of Hematology, University Hospital Le Fe and School of Medicine and Dentistry, Catholic University of Valencia, CIBERONC CB16/12/00284, Valencia, Spain.ORCID 0000-0002-8354-768X
Verónica González-CalleHematology Department, IBSAL, Instituto de Biología Molecular y Celular del Cáncer-Consejo Superior de Investigaciones Científicas (IBMCC-CSIC), Centro de Investigación Biomédica en Red de Cáncer (CIBERONC).ORCID 0000-0002-5493-6707
Isabel KrsnikHospital Puerta de Hierro, Madrid, Spain.ORCID 0000-0002-2912-5072
Valentín CabañasHospital Universitario Virgen de la Arrixaca, IMIB, Murcia, Spain.ORCID 0000-0002-6248-2549
Luis PalomeraHospital Clínico Universitario Lozano Blesa, Zaragoza, Spain.
José-María MoraledaHospital Universitario Virgen de la Arrixaca, IMIB, Murcia, Spain.ORCID 0000-0001-9080-1466
Joan BargayHospital Son Llatzer, Palma de Mallorca, Spain.
María-Teresa CedenaHospital Universitario 12 de Octubre, Complutense University, i+12, CNIO, CIBERONC CB16/12/00369, Madrid, Spain.ORCID 0000-0001-5851-3720
Bruno PaivaClínica Universidad de Navarra, CIMA, IDISNA, CIBERONC CB16/12/00369, Pamplona, Spain.ORCID 0000-0003-1977-3815
Laura RosiñolHospital Clinic, Institut d'Investigacions Biomédiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain; and.
Joan BladéHospital Clinic, Institut d'Investigacions Biomédiques August Pi I Sunyer (IDIBAPS), Barcelona, Spain; and.
Jesús San MiguelClínica Universidad de Navarra, CIMA, IDISNA, CIBERONC CB16/12/00369, Pamplona, Spain.ORCID 0000-0002-9183-4857
Juan-José LahuertaInstituto de Investigación del Hospital Universitario 12 de Octubre, CIBERONC, Madrid, Spain.ORCID 0000-0002-3393-9570
María-Victoria MateosHematology Department, IBSAL, Instituto de Biología Molecular y Celular del Cáncer-Consejo Superior de Investigaciones Científicas (IBMCC-CSIC), Centro de Investigación Biomédica en Red de Cáncer (CIBERONC).ORCID 0000-0003-2390-1218
Consejo Superior de Investigaciones Científicas · ESHospital Universitario 12 De Octubre · ESClinica Universidad de Navarra · ESComplejo Hospitalario de Salamanca · ESConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESHospital Universitario Virgen de la Arrixaca · ESHospital Clínico San Carlos · ESHospital Clínico Universitario Lozano Blesa · ESHospital Son Llatzer · ESHospital Universitario de Canarias · ESHospital Universitario Puerta de Hierro Majadahonda · ESHospital Universitario Virgen de las Nieves · ESHospital Universitario Virgen del Rocío · ESInstitut Català d'Oncologia · ESInstitut d'Investigació Biomédica de Bellvitge · ESUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Monitoring of the monoclonal protein (M-protein) by electrophoresis and/or immunofixation (IFE) has long been used to assess treatment response in multiple myeloma (MM). However, with the use of highly effective therapies, the M-protein becomes frequently undetectable, and more sensitive methods had to be explored. We applied IFE and mass spectrometry (EXENT&FLC-MS) in serum samples from newly diagnosed MM patients enrolled in the PETHEMA/GEM2012MENOS65 obtained at baseline (n = 223), and after induction (n = 183), autologous stem cell transplantation (n = 173), and consolidation (n = 173). At baseline, the isotypes identified with both methods fully matched in 82.1% of samples; in the rest but 2 cases, EXENT&FLC-MS provided additional information to IFE with regards to the M-protein(s). Overall, the results of EXENT&FLC-MS and IFE were concordant in >80% of cases, being most discordances due to EXENT&FLC-MS+ but IFE- cases. After consolidation, IFE was not able to discriminate 2 cohorts with different median progression-free survival (PFS), but EXENT&FLC-MS did so; furthermore, among IFE- patients, EXENT&FLC-MS identified 2 groups with significantly different median PFS (P = .0008). In conclusion, compared with IFE, EXENT&FLC-MS is more sensitive to detect the M-protein of patients with MM, both at baseline and during treatment, and provides a more accurate prediction of patients' outcome. This trial was registered at www.clinicaltrials.gov as #NCT01916252.

Indexed as

Hematopoietic Stem Cell TransplantationMultiple MyelomaAntibodies, MonoclonalHumansImmunoglobulin Light ChainsMass SpectrometryTransplantation, AutologousAntibodies, MonoclonalImmunoglobulin Light Chains

Identifiers

PMID35157768
PMCPMC9198943
OpenAlexW4213381063

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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.