Evidence map›Paper›PMID 33661537›Full record

ReviewAmerican journal of hematology2021

2021 Update on Diffuse large B cell lymphoma: A review of current data and potential applications on risk stratification and management.

Sandra Susanibar-Adaniya, Stefan K Barta

Abstract readReview
In one paragraph

Review in American journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 217 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
217citing papers in PubMed, 6 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

217 citing papers in PubMed, 6 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Pooled it
  4. Guideline
  5. Prophylaxis forBMJ open · 2023
    Pooled it
  6. Pooled it
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  9. Brentuximab Vedotin Combination for Relapsed Diffuse Large B-Cell Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
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  14. Article
  15. Expression and diagnostic significance of plasma exosomal RNA in diffuse large B-cell lymphoma.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  16. Experimental and therapeutic medicine · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Review

157 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

2 authors.

Sandra Susanibar-AdaniyaDepartment of Hematology/Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.
Stefan K BartaDepartment of Hematology/Oncology, University of Pennsylvania, Philadelphia, Pennsylvania.ORCID 0000-0002-3280-5271

Funding

CANCER RESEARCH TRAINING PROGRAMT32CA009615 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Gregory L Beatty, MICHAEL D HOGARTY · 1988 to 2026
$10.4M
NRSA Training CoreTL1TR001880 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$10.0M
Abramson Cancer Center's Ruth L. Kirschstein National Research Service Award (NRSA) Institutional T32 Research Training Grant 5T32CA009615-30 and National Center for Advancing Translational Sciences of the National Institutes of Health TL1TR001880 5T32CA009615-30Abramson Cancer Center's Ruth L. Kirschstein National Research Service Award (NRSA) Institutional T32 Research Training Grant 5T32CA009615-30 and National Center for Advancing Translational Sciences of the National Institutes of Health TL1TR001880 TL1TR001880NCATS NIH HHS TL1 TR001880NCI NIH HHS T32 CA009615
6 · The paper itself

Abstract

Diffuse large B cell lymphoma (DLBCL), the most common type of Non-Hodgkin lymphoma (NHL), comprises a heterogeneous group of diseases with different biology, clinical presentations, and response to treatment. R-CHOP remains the mainstay of therapy and can achieve long-term disease control in nearly 90% of patients presenting with limited-stage and in up to 60% of those presenting with advanced stages. Advances on the understanding of the genetic landscape and molecular features of DLBCL have identified high-risk subsets with poor outcomes to chemo-immunotherapy that are actively being studied in clinical trials. Novel therapies could potentially improve outcomes for patients with high-risk disease. Studies evaluating risk-adapted therapy based on classification by cell of origin (COO) and molecular features are ongoing. Developments in the fields of immunotherapy, mostly with adoptive T-cell therapy, have significantly improved the outcomes of patients with relapsed refractory disease. In this review, we will summarize the recent data and discuss ongoing efforts to improve DLBCL treatment in the frontline and relapsed refractory settings.

Indexed as

Lymphoma, Large B-Cell, DiffuseAntineoplastic Combined Chemotherapy ProtocolsB-Lymphocyte SubsetsCell LineageCombined Modality TherapyCyclophosphamideDisease ManagementDNA, NeoplasmDoxorubicinExome SequencingGenes, bcl-2Genes, mycHematopoietic Stem Cell TransplantationHumansImmunotherapy, AdoptiveNeoplasm StagingCyclophosphamideDNA, NeoplasmDoxorubicinPrednisoneRituximabVincristine

Identifiers

PMID33661537
PMCPMC8172085

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.