Evidence map›Paper›PMID 36854569›Full record

ArticleJournal for immunotherapy of cancer2023

Venetoclax improves CD20 immunotherapy in a mouse model of MYC/BCL2 double-expressor diffuse large B-cell lymphoma.

Javier Melchor, Marcos Garcia-Lacarte, Sara C Grijalba, Adrián Arnaiz-Leché, Marién Pascual, Carlos Panizo, Oscar Blanco, Victor Segura, Francisco J Novo, Juan Garcia Valero and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% 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.

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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
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  3. Article
  4. Article
  5. Article
  6. Review
  7. 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

13 authors at 5 institutions in 1 country.

Javier MelchorDepartment of Biochemistry and Genetics, Universidad de Navarra, Pamplona, Spain.ORCID 0000-0003-1793-4152
Marcos Garcia-LacarteDepartment of Biochemistry and Genetics, Universidad de Navarra, Pamplona, Spain.ORCID 0000-0003-0614-8682
Sara C GrijalbaDepartment of Biochemistry and Genetics, Universidad de Navarra, Pamplona, Spain.ORCID 0000-0003-4542-1805
Adrián Arnaiz-LechéDepartment of Biochemistry and Genetics, Universidad de Navarra, Pamplona, Spain.ORCID 0000-0002-0687-0053
Marién PascualHemato-Oncology Program, Center for Applied Medical Research (CIMA), Pamplona, Spain.ORCID 0000-0002-1678-1054
Carlos PanizoNavarra Institute for Health Research (IdiSNA), Pamplona, Spain.ORCID 0000-0002-3945-585X
Oscar BlancoDepartment of Pathology, Universidad de Salamanca, Salamanca, Spain.ORCID 0000-0002-2667-0489
Victor SeguraBio-informatic Unit, Center for Applied Medical Research (CIMA), Pamplona, Spain.ORCID 0000-0002-7740-6290
Francisco J NovoDepartment of Biochemistry and Genetics, Universidad de Navarra, Pamplona, Spain.ORCID 0000-0003-4961-3097
Juan Garcia ValeroDepartment of Hematology-Oncology, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0003-3193-9099
Patricia Pérez-GalánDepartment of Hematology-Oncology, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.ORCID 0000-0003-3895-5024
Jose A Martinez-ClimentHemato-Oncology Program, Center for Applied Medical Research (CIMA), Pamplona, Spain.ORCID 0000-0002-7938-3950
Sergio RoaDepartment of Biochemistry and Genetics, Universidad de Navarra, Pamplona, Spain sroa@unav.es.ORCID 0000-0003-1095-0715
Instituto de Salud Carlos III · ESNavarre Institute of Health Research · ESBiogipuzkoa Health Research Institute · ESUniversidad de Navarra · ESUniversidad de Salamanca · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundApproximately one-third of diffuse large B cell lymphoma (DLBCL) patients exhibit co-expression of MYC and BCL2 (double-expressor lymphoma, DEL) and have a dismal prognosis. Targeted inhibition of the anti-apoptotic protein BCL2 with venetoclax (ABT-199) has been approved in multiple B-cell malignancies and is currently being investigated in clinical trials for DLBCL. Whether BCL2 anti-apoptotic function represents a multifaceted vulnerability for DEL-DLBCL, affecting both lymphoma B cells and T cells within the tumor microenvironment, remains to be elucidated.

methodsHere, we present novel genetically engineered mice that preclinically recapitulate DEL-DLBCL lymphomagenesis, and evaluate their sensitivity ex vivo and in vivo to the promising combination of venetoclax with anti-CD20-based standard immunotherapy.

resultsVenetoclax treatment demonstrated specific killing of MYC

conclusionsThese results suggest that the combination of anti-CD20-based immunotherapy and BCL2 inhibition leads to cooperative immunomodulatory effects and improved preclinical responses, which may offer promising therapeutic opportunities for DEL-DLBCL patients.

Indexed as

Bridged Bicyclo Compounds, HeterocyclicImmunotherapyLymphoma, Large B-Cell, DiffuseAnimalsDisease Models, AnimalMiceProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycSulfonamidesTumor MicroenvironmentBridged Bicyclo Compounds, HeterocyclicProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycSulfonamidesvenetoclaxB-lymphocytesCD4-CD8 ratiodrug evaluation, preclinicalhematologic neoplasmsimmunotherapy

Identifiers

PMID36854569
PMCPMC9980368
OpenAlexW4322619333

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.