Evidence map›Paper›PMID 34398302›Full record

ArticleCancer immunology, immunotherapy : CII2021

CD16xCD33 Bispecific Killer Cell Engager (BiKE) as potential immunotherapeutic in pediatric patients with AML and biphenotypic ALL.

Sarah B Reusing, Dan A Vallera, Angela R Manser, Titus Vatrin, Sanil Bhatia, Martin Felices, Jeffrey S Miller, Markus Uhrberg, Florian Babor

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. 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 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 43 citations in OpenAlex.

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  16. The potential of monoclonal antibodies for colorectal cancer therapy.Medical oncology (Northwood, London, England) · 2023
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  19. Human natural killer cells: Form, function, and development.The Journal of allergy and clinical immunology · 2023
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Sarah B ReusingInstitute for Transplantation Diagnostics and Cell Therapeutics, Heinrich Heine University, Düsseldorf, Germany.
Dan A ValleraDepartment of Therapeutic Radiology-Radiation Oncology, Masonic Cancer Center, University of Minnesota, Minneapolis, MN, USA.
Angela R ManserInstitute for Transplantation Diagnostics and Cell Therapeutics, Heinrich Heine University, Düsseldorf, Germany.
Titus VatrinDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Centre for Child and Adolescent Health, Medical Faculty, Heinrich Heine University, Moorenstraße 5, 40225, Düsseldorf, Germany.
Sanil BhatiaDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Centre for Child and Adolescent Health, Medical Faculty, Heinrich Heine University, Moorenstraße 5, 40225, Düsseldorf, Germany.
Martin FelicesDepartment of Medicine, Division of Hematology, Oncology and Transplantation, Minneapolis, MN, USA.
Jeffrey S MillerDepartment of Medicine, Division of Hematology, Oncology and Transplantation, Minneapolis, MN, USA.
Markus UhrbergInstitute for Transplantation Diagnostics and Cell Therapeutics, Heinrich Heine University, Düsseldorf, Germany.
Florian BaborDepartment of Pediatric Oncology, Hematology and Clinical Immunology, Centre for Child and Adolescent Health, Medical Faculty, Heinrich Heine University, Moorenstraße 5, 40225, Düsseldorf, Germany. Florian.Babor@med.uni-duesseldorf.de.ORCID http://orcid.org/0000-0002-6078-9993
Heinrich Heine University Düsseldorf · DEMinnesota Oncology · USUniversity of Minnesota Medical Center · US

Funding

Trial Design and Biostatistical Support CoreP01CA065493 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI J SUNIL RAO · 1995 to 2026
$48.2M
Therapeutic Potential of Adaptive NK Cells in Cancer and TransplantationP01CA111412 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI GELLER, MELISSA ANN · 2005 to 2025
$38.2M
NCI NIH HHS P01 CA065493NCI NIH HHS P01 CA111412
6 · The paper itself

Abstract

Similar to pediatric acute myeloid leukemia (AML) the subgroup of biphenotypic acute lymphoblastic leukemia (ALL) is a rare complex entity with adverse outcome, characterized by the surface expression of CD33. Despite novel and promising anti-CD19 targeted immunotherapies such as chimeric antigen receptor T cells and bispecific anti-CD19/CD3 antibodies, relapse and resistance remain a major challenge in about 30% to 60% of patients. To investigate the potential role of the fully humanized bispecific antibody CD16 × CD33 (BiKE) in children with CD33

Indexed as

Antibodies, BispecificCell LineCell Line, TumorCytotoxicity, ImmunologicGPI-Linked ProteinsHL-60 CellsHumansImmunotherapyKiller Cells, NaturalLeukemia, Myeloid, AcuteLymphocyte ActivationReceptors, IgGSialic Acid Binding Ig-like Lectin 3Antibodies, BispecificCD33 protein, humanFCGR3B protein, humanGPI-Linked ProteinsReceptors, IgGSialic Acid Binding Ig-like Lectin 3Antibody therapyBiKEBiphenotypic ALLBispecific antibodiesCD33NK cells

Identifiers

PMID34398302
PMCPMC8571204
OpenAlexW3195161684

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.