Evidence map›Paper›PMID 39534383›Full record

ArticleHemaSphere2024

Prognostic risk and survival of asymptomatic IgM monoclonal gammopathy: Results from a Spanish Multicenter Registry.

David F Moreno, Cristina Jiménez, Fernando Escalante, Elham Askari, Marta Castellanos-Alonso, Mario Arnao, Ángela Heredia, Miguel Á Canales, Magdalena Alcalá, Arancha Bermúdez and 8 more

Abstract read
In one paragraph

Article in HemaSphere, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

18 authors.

David F MorenoHematology Department, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) Universitat de Barcelona Barcelona Spain.ORCID 0000-0002-1752-3081
Cristina JiménezHematology Department University Hospital of Salamanca, Research Biomedical Institute of Salamanca (IBSAL), Accelerator project, Centro de Investigación Biomédica en Red-Cáncer (CIBERONC) CB16/12/00369 and Center for Cancer Research-IBMCC (USAL-CSIC) Salamanca Spain.
Fernando EscalanteHematology Department Unidad i + i, Complejo Asistencial Universitario de León León Spain.
Elham AskariHematology Department Hospital Universitario Fundación Jiménez Díaz Madrid Spain.
Marta Castellanos-AlonsoHematology Department Unidad i + i, Complejo Asistencial Universitario de León León Spain.
Mario ArnaoHematology Department, Hospital La Fe Centro de Investigación Biomédica en Red-Cáncer (CIBERONC) Valencia Spain.
Ángela HerediaHematology Department Hospital Virgen de la Arrixaca, IMIB Murcia Spain.
Miguel Á CanalesHematology Department Clínica Universidad de Navarra, Centro de Investigación Biomédica en Red-Cáncer (CIBERONC) Pamplona Spain.
Magdalena AlcaláHematology Department Hospital Regional Universitario de Málaga Málaga Spain.
Arancha BermúdezHematology Department University Hospital Marqués de Valdecilla, IDIVAL Santander Spain.
Ana Saus CarreresHematology Department Hospital Clínico Universitario Valencia Spain.
María CasanovaHematology Department Hospital Costa del Sol Marbella Marbella Spain.
Luis PalomeraHematology Department Hospital Clínico Lozano Blesa Zaragoza Spain.
Cristina MotllóHematology Department Hospital Sant Joan de Déu-Fundació Althaia Manresa Spain.
Ricarda García-SánchezHematology Department Hospital Virgen de la Victoria Málaga Spain.
Pablo Ríos RullHematology Department Hospital Nuestra Señora de la Candelaria Canarias Spain.
Ramón García-SanzHematology Department University Hospital of Salamanca, Research Biomedical Institute of Salamanca (IBSAL), Accelerator project, Centro de Investigación Biomédica en Red-Cáncer (CIBERONC) CB16/12/00369 and Center for Cancer Research-IBMCC (USAL-CSIC) Salamanca Spain.
Carlos Fernández de LarreaHematology Department, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS) Universitat de Barcelona Barcelona Spain.ORCID 0000-0003-4930-9255

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Asymptomatic IgM gammopathy encompasses IgM monoclonal gammopathy of undetermined significance (MGUS) and asymptomatic Waldenström macroglobulinemia (AWM), both having a risk of progression to symptomatic disease. Here, we assessed the risk of progression and the mortality of 956 patients with asymptomatic IgM gammopathy across 25 Spanish centers. After a median follow-up of 5.7 years, 156 patients progressed, most of them to symptomatic WM (SWM). The cumulative incidence of progression was 13% and 20% at 5 and 10 years, respectively. The serum IgM ≥10 g/L, bone marrow (BM) infiltration ≥20%, β2-microglobulin ≥3 mg/L, and albumin <4 g/dL were the most potent predictors of disease progression in a multivariate Cox regression model, allowing the identification of three risk categories. The probability of progression to symptomatic disease at 5 years was 4.5%, 15.7%, and 42.8% for low-, intermediate-, and high-risk groups, respectively. In patients without a BM evaluation, the presence of none or 1 risk factor and 2 or 3 risk factors conferred a progression risk of 6% and 27% at 5 years, respectively. The model was independent of the presence of

Identifiers

PMID39534383
PMCPMC11555297

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.