Evidence map›Paper›PMID 32457743›Full record

ReviewFrontiers in immunology2020

Bispecific, T-Cell-Recruiting Antibodies in B-Cell Malignancies.

Margaux Lejeune, Murat Cem Köse, Elodie Duray, Hermann Einsele, Yves Beguin, Jo Caers

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
6.7field-weighted citation impact, top 2% 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

54 citing papers in PubMed, 83 citations in OpenAlex.

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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

6 authors at 3 institutions in 2 countries.

Margaux LejeuneLaboratory of Hematology, GIGA I3, University of Liège, Liège, Belgium.
Murat Cem KöseLaboratory of Hematology, GIGA I3, University of Liège, Liège, Belgium.
Elodie DurayLaboratory of Hematology, GIGA I3, University of Liège, Liège, Belgium.
Hermann EinseleDepartment of Internal Medicine II, University of Würzburg, Würzburg, Germany.
Yves BeguinLaboratory of Hematology, GIGA I3, University of Liège, Liège, Belgium.
Jo CaersLaboratory of Hematology, GIGA I3, University of Liège, Liège, Belgium.
University of Liège · BECentre Hospitalier Universitaire de Liège · BEUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bispecific antibodies (BsAbs) are designed to recognize and bind to two different antigens or epitopes. In the last few decades, BsAbs have been developed within the context of cancer therapies and in particular for the treatment of hematologic B-cell malignancies. To date, more than one hundred different BsAb formats exist, including bispecific T-cell engagers (BiTEs), and new constructs are constantly emerging. Advances in protein engineering have enabled the creation of BsAbs with specific mechanisms of action and clinical applications. Moreover, a better understanding of resistance and evasion mechanisms, as well as advances in the protein engineering and in immunology, will help generating a greater variety of BsAbs to treat various cancer types. This review focuses on T-cell-engaging BsAbs and more precisely on the various BsAb formats currently being studied in the context of B-cell malignancies, on ongoing clinical trials and on the clinical concerns to be taken into account in the development of new BsAbs.

Indexed as

AnimalsAntibodies, BispecificB-LymphocytesHematologic NeoplasmsHumansImmunoglobulin Fc FragmentsImmunotherapyLeukemia, Lymphocytic, Chronic, B-CellLymphoma, Non-HodgkinMultiple MyelomaPrecursor Cell Lymphoblastic Leukemia-LymphomaT-LymphocytesAntibodies, BispecificImmunoglobulin Fc Fragmentsbispecific antibodiesbispecific T-cell engagerBiTEclinical developmentconcernsleukemialymphomamyeloma

Identifiers

PMID32457743
PMCPMC7221185
OpenAlexW3023104624

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.