Evidence map›Paper›PMID 40357216›Full record

ArticleHemaSphere2025

Biomarker-adapted treatment in high-risk large B-cell lymphoma.

Sirpa Leppä, Leo Meriranta, Maare Arffman, Judit Jørgensen, Marja-Liisa Karjalainen-Lindsberg, Klaus Beiske, Mette Pedersen, Kristina Drott, Annika Pasanen, Kristiina Karihtala and 11 more

Abstract read
In one paragraph

Article in HemaSphere, 2025. 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. Review
  2. Article
  3. Article
  4. 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

21 authors.

Sirpa LeppäDepartment of Oncology Helsinki University Hospital Comprehensive Cancer Centre Helsinki Finland.ORCID 0000-0002-8265-511X
Leo MerirantaDepartment of Oncology Helsinki University Hospital Comprehensive Cancer Centre Helsinki Finland.ORCID https://orcid.org/0000-0002-6378-5381
Maare ArffmanDepartment of Oncology Helsinki University Hospital Comprehensive Cancer Centre Helsinki Finland.ORCID https://orcid.org/0009-0004-1837-1587
Judit JørgensenDepartment of Hematology Aarhus University Hospital Aarhus Denmark.
Marja-Liisa Karjalainen-LindsbergDepartment of Pathology Helsinki University Hospital Helsinki Finland.
Klaus BeiskeDepartment of Pathology Oslo University Hospital Oslo Norway.
Mette PedersenDepartment of Pathology Zealand University Hospital Roskilde Denmark.
Kristina DrottDepartment of Oncology Skane University Hospital Lund Sweden.
Annika PasanenDepartment of Oncology Helsinki University Hospital Comprehensive Cancer Centre Helsinki Finland.
Kristiina KarihtalaDepartment of Oncology Helsinki University Hospital Comprehensive Cancer Centre Helsinki Finland.
Susanna MannistoDepartment of Oncology Helsinki University Hospital Comprehensive Cancer Centre Helsinki Finland.
Bente WoldDepartment of Oncology Oslo University Hospital Oslo Norway.
Marianne BrodtkorbDepartment of Oncology Oslo University Hospital Oslo Norway.
Unn-Merete FagerliDepartment of Oncology St. Olavs Hospital Trondheim Norway.
Thomas Stauffer LarsenDepartment of Hematology Odense University Hospital Odense Denmark.
Lars MunksgaardDepartment of Hematology Zealand University Hospital Roskilde Denmark.
Kaisa SunelaDepartment of Oncology Tampere University Hospital Tampere Finland.
Øystein FlugeDepartment of Oncology Haukeland University Hospital Bergen Norway.
Sirkku JyrkkiöDepartment of Oncology Turku University Hospital Turku Finland.
Peter BrownDepartment of Hematology Rigshospitalet Copenhagen Denmark.
Harald HolteDepartment of Oncology Oslo University Hospital Oslo Norway.ORCID https://orcid.org/0000-0001-9799-9428

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Survival rates for patients with high-risk large B-cell lymphoma (LBCL), particularly those with biological risk factors, remain inadequate. We conducted a biomarker-driven phase II trial involving 123 high-risk patients aged 18-64 with LBCL. Based on their biological risk profiles, patients received either R-CHOEP-14 (without risk factors) or DA-EPOCH-R-based regimens (with risk factors). Biological high-risk factors included

Identifiers

PMID40357216
PMCPMC12066987

What OpenQuestion holds

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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.