Evidence map›Paper›PMID 38672662›Full record

ReviewCancers2024

T-Cell Engagers-The Structure and Functional Principle and Application in Hematological Malignancies.

Paweł Cech, Katarzyna Skórka, Laura Dziki, Krzysztof Giannopoulos

Open access · goldAbstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
6.8field-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

23 citing papers in PubMed, 24 citations in OpenAlex.

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  11. Canadian oncology nursing journal = Revue canadienne de nursing oncologique · 2026
    Article
  12. A real-world analysis of adverse events and operational impacts of using T-cell engager therapy in an oncology setting.Canadian oncology nursing journal = Revue canadienne de nursing oncologique · 2026
    Article
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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

4 authors at 1 institution in 1 country.

Paweł CechDepartment of Experimental Hematooncology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0009-0002-9931-3543
Katarzyna SkórkaDepartment of Experimental Hematooncology, Medical University of Lublin, 20-093 Lublin, Poland.
Laura DzikiDepartment of Experimental Hematooncology, Medical University of Lublin, 20-093 Lublin, Poland.
Krzysztof GiannopoulosDepartment of Experimental Hematooncology, Medical University of Lublin, 20-093 Lublin, Poland.ORCID 0000-0003-0135-4030
Medical University of Lublin · PL

Funding

Medical University of Lublin DS462
6 · The paper itself

Abstract

Recent advancements in cancer immunotherapy have made directing the cellular immune response onto cancer cells a promising strategy for the treatment of hematological malignancies. The introduction of monoclonal antibody-based (mAbs) targeted therapy has significantly improved the prognosis for hematological patients. Facing the issues of mAb-based therapies, a novel bispecific antibody (BsAb) format was developed. T-cell engagers (TCEs) are BsAbs, which simultaneously target tumor-associated antigens on tumor cells and CD3 molecules present on T-cells. This mechanism allows for the direct activation of T-cells and their anti-tumor features, ultimately resulting in the lysis of tumor cells. In 2014, the FDA approved blinatumomab, a TCE directed to CD3 and CD19 for treatment of acute lymphoblastic leukemia. Since then, numerous TCEs have been developed, allowing for treating different hematological malignancies such as acute myeloid leukemia, multiple myeloma, and non-Hodgkin lymphoma and Hodgkin lymphoma. As of November 2023, seven clinically approved TCE therapies are on the market. TCE-based therapies still have their limitations; however, improving the properties of TCEs, as well as combining TCE-based therapies with other forms of treatment, give hope to find the cures for currently terminal diseases. In this paper, we summarized the technical basis of the TCE technology, its application in hematology, and its current issues and prospects.

Indexed as

bi-specific antibody (BsAb)bi-specific T-cell engager (BiTE)blinatumomabimmunotherapies in hematologyT-cell engager (TCE)T-cell engaging therapies

Identifiers

PMID38672662
PMCPMC11048836
OpenAlexW4395004408

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.