Evidence map›Paper›PMID 32856140›Full record

ReviewAnnals of hematology2020

Concepts in immuno-oncology: tackling B cell malignancies with CD19-directed bispecific T cell engager therapies.

Andreas Viardot, Franco Locatelli, Julia Stieglmaier, Faraz Zaman, Elias Jabbour

Abstract readReview
In one paragraph

Review in Annals of hematology, 2020. 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
–field-weighted citation impact
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.

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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

5 authors.

Andreas ViardotDepartment of Internal Medicine III, University Hospital Ulm, Ulm, Germany.
Franco LocatelliDepartment of Pediatric Hematology and Oncology, IRCCS Bambino Gesù Children's Hospital, Sapienza, University of Rome, Rome, Italy.
Julia StieglmaierEarly Development Hematology/Oncology, Amgen Research (Munich) GmbH, Staffelseestraße 2, 81477, Munich, Germany. jstieglm@amgen.com.
Faraz ZamanAmgen Inc., Thousand Oaks, CA, USA.
Elias JabbourDepartment of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The B cell surface antigen CD19 is a target for treating B cell malignancies, such as B cell precursor acute lymphoblastic leukemia and B cell non-Hodgkin lymphoma. The BiTE® immuno-oncology platform includes blinatumomab, which is approved for relapsed/refractory B cell precursor acute lymphoblastic leukemia and B cell precursor acute lymphoblastic leukemia with minimal residual disease. Blinatumomab is also being evaluated in combination with other agents (tyrosine kinase inhibitors, checkpoint inhibitors, and chemotherapy) in various treatment settings, including frontline protocols. An extended half-life BiTE molecule is also under investigation. Patients receiving blinatumomab may experience cytokine release syndrome and neurotoxicity; however, these events may be less frequent and severe than in patients receiving other CD19-targeted immunotherapies, such as chimeric antigen receptor T cell therapy. We review BiTE technology for treating malignancies that express CD19, analyzing the benefits and limitations of this bispecific T cell engager platform from clinical experience with blinatumomab.

Indexed as

AdolescentAdrenal Cortex HormonesAdultAntibodies, BispecificAntigens, CD19Antigens, NeoplasmAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsB-Lymphocyte SubsetsChildClinical Trials as TopicCombined Modality TherapyCost-Benefit AnalysisCytokine Release SyndromeDrug CostsHumansAdrenal Cortex HormonesAntibodies, BispecificAntigens, CD19Antigens, NeoplasmAntineoplastic Agents, ImmunologicalblinatumomabCD19 molecule, humanAcute lymphoblastic leukemiaB cell malignanciesBispecific T cell engagerBiTE moleculeBlinatumomabCD19Non-Hodgkin lymphoma

Identifiers

PMID32856140
PMCPMC7481145

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Registered trials

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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.