Evidence map›Paper›PMID 38888359›Full record

ArticleCancer medicine2024

Revisiting beta-2 microglobulin as a prognostic marker in diffuse large B-cell lymphoma.

Jelena Jelicic, Karen Juul-Jensen, Zoran Bukumiric, Mikkel Runason Simonsen, Michael Roost Clausen, Ahmed Ludvigsen Al-Mashhadi, Robert Schou Pedersen, Christian Bjørn Poulsen, Anne Ortved Gang, Peter Brown and 2 more

Abstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 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.

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

11 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  5. Article
  6. Development and validation of a prognostic nomogram for diffuse large B-cell lymphoma: a multicenter cohort study from Northern China.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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  7. Review
  8. Review
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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

12 authors.

Jelena JelicicDepartment of Hematology, Odense University Hospital, Odense, Denmark.ORCID 0000-0001-7695-8539
Karen Juul-JensenDepartment of Hematology, Odense University Hospital, Odense, Denmark.
Zoran BukumiricFaculty of Medicine, Institute for Medical Statistics and Informatics, University of Belgrade, Belgrade, Serbia.
Mikkel Runason SimonsenDepartment of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Michael Roost ClausenDepartment of Hematology, Vejle Hospital, Sygehus Lillebaelt, Vejle, Denmark.
Ahmed Ludvigsen Al-MashhadiDepartment of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
Robert Schou PedersenDepartment of Hematology, Regional Hospital Gødstrup, Herning, Denmark.
Christian Bjørn PoulsenDepartment of Hematology, Zealand University Hospital, Roskilde, Denmark.
Anne Ortved GangDepartment of Clinical Medicine, University of Copenhagen, Kobenhavn, Denmark.
Peter BrownDepartment of Clinical Medicine, University of Copenhagen, Kobenhavn, Denmark.ORCID 0000-0002-6522-4086
Tarec Christoffer El-GalalyDepartment of Hematology, Odense University Hospital, Odense, Denmark.
Thomas Stauffer LarsenDepartment of Hematology, Odense University Hospital, Odense, Denmark.ORCID 0000-0002-8418-6708

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSeveral clinical prognostic models for diffuse large B-cell lymphoma (DLBCL) have been proposed, including the most commonly used International Prognostic Index (IPI), the National Comprehensive Cancer Network IPI (NCCN-IPI), and models incorporating beta-2 microglobulin (β2M). However, the role of β2M in DLBCL patients is not fully understood.

methodsWe identified 6075 patients with newly diagnosed DLBCL treated with immunochemotherapy registered in the Danish Lymphoma Registry.

resultsA total of 3232 patients had data available to calculate risk scores from each of the nine considered risk models for DLBCL, including a model developed from our population. Three of four models with β2M and NCCN-IPI performed better than the International Prognostic Indexes (IPI, age-adjusted IPI, and revised IPI). Five-year overall survival for high- and low-risk patients were 43.6% and 86.4% for IPI and 34.9% and 96.2% for NCCN-IPI. In univariate analysis, higher levels of β2M were associated with inferior survival, higher tumor burden (advanced clinical stage and bulky disease), previous malignancy and increased age, and creatinine levels. Furthermore, we developed a model (β2M-NCCN-IPI) by adding β2M to NCCN-IPI (c-index 0.708) with improved discriminatory ability compared to NCCN-IPI (c-index 0.698, p < 0.05) and 5-year OS of 33.1%, 56.2%, 82.4%, and 96.4% in the high, high-intermediate, low-intermediate and low-risk group, respectively.

conclusionInternational Prognostic Indices, except for NCCN-IPI, fail to accurately discriminate risk groups in the rituximab era. β2M, a readily available marker, could improve the discriminatory performance of NCCN-IPI and should be re-evaluated in the development setting of future models for DLBCL.

Indexed as

beta 2-MicroglobulinBiomarkers, TumorLymphoma, Large B-Cell, DiffuseAdolescentAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsDenmarkFemaleHumansMaleMiddle AgedNeoplasm StagingPrognosisRegistriesB2M protein, humanbeta 2-MicroglobulinBiomarkers, Tumornon‐Hodgkin lymphomaprognosisprognostic factorsrisk model

Identifiers

PMID38888359
PMCPMC11184650

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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.