Evidence map›Paper›PMID 32581054›Full record

ArticleJournal for immunotherapy of cancer2020

CD3xCD19 DART molecule treatment induces non-apoptotic killing and is efficient against high-risk chemotherapy and venetoclax-resistant chronic lymphocytic leukemia cells.

Anne W J Martens, Susanne R Janssen, Ingrid A M Derks, Homer C Adams Iii, Liat Izhak, Roel van Kampen, Sanne H Tonino, Eric Eldering, Gerritje J W van der Windt, Arnon P Kater

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.3field-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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Ectopic expression of cGAS inJournal for immunotherapy of cancer · 2023
    Article
  5. Review
  6. Article
  7. Article
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  9. Review
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  11. Immunomodulatory Drugs for the Treatment of B Cell Malignancies.International journal of molecular sciences · 2021
    Review
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  13. Article
  14. Article
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  16. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Anne W J MartensDepartment of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam UMC, Amsterdam, The Netherlands.ORCID 0000-0003-0858-2482
Susanne R JanssenDepartment of Hematology, Cancer Center Amsterdam and Lymphoma and Myeloma Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Ingrid A M DerksDepartment of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam UMC, Amsterdam, The Netherlands.
Homer C Adams IiiJanssen Pharmaceutical Companies of Johnson and Johnson, Philadelphia, Pennsylvania, USA.
Liat IzhakJanssen Pharmaceutical Companies of Johnson and Johnson, Philadelphia, Pennsylvania, USA.
Roel van KampenDepartment of Internal Medicine, Zuyderland Medical Centre Heerlen, Heerlen, The Netherlands.
Sanne H ToninoDepartment of Hematology, Cancer Center Amsterdam and Lymphoma and Myeloma Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Eric ElderingDepartment of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam UMC, Amsterdam, The Netherlands.
Gerritje J W van der Windt *Department of Experimental Immunology, Amsterdam Infection & Immunity Institute, Amsterdam UMC, Amsterdam, The Netherlands.
Arnon P Kater *Department of Hematology, Cancer Center Amsterdam and Lymphoma and Myeloma Center Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands a.p.kater@amsterdamumc.nl.
Amsterdam University Medical Centers · NLJohnson & Johnson (United States) · USZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBispecific antibodies are promising new therapeutics in B cell malignancies. Whether they lead to potent T cell activation despite described T cell dysfunction in chronic lymphocytic leukemia (CLL), and are able to effectively target high-risk or venetoclax-resistant samples, is currently unknown.

methodsCD19

resultsHere, we report that a bispecific CD3xCD19 DART mediates efficient killing by HD T cells of CD19

conclusionsThese data show that CD3xCD19 DART in CLL leads to robust T cell activation and lysis of high-risk venetoclax resistant CLL cells through a non-apoptotic mechanism.

Indexed as

AdultAgedAged, 80 and overAntibodies, BispecificAntigens, CD19Antineoplastic AgentsAntineoplastic Combined Chemotherapy ProtocolsBridged Bicyclo Compounds, HeterocyclicCase-Control StudiesCD3 ComplexCD8-Positive T-LymphocytesCytotoxicity, ImmunologicFemaleFollow-Up StudiesHumansImmunoglobulin Heavy ChainsAntibodies, BispecificAntigens, CD19Antineoplastic AgentsBridged Bicyclo Compounds, HeterocyclicCD3 ComplexImmunoglobulin Heavy ChainsImmunoglobulin Variable RegionSulfonamidesTP53 protein, humanTumor Suppressor Protein p53venetoclaximmunologyimmunotherapyoncologyT-Lymphocytes

Identifiers

PMID32581054
PMCPMC7319711
OpenAlexW3038016373

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.