Evidence map›Paper›PMID 35906791›Full record

ReviewJournal of clinical pharmacy and therapeutics2022

The pharmacology of blinatumomab: state of the art on pharmacodynamics, pharmacokinetics, adverse drug reactions and evaluation in clinical trials.

Pauline Mocquot, Yasmine Mossazadeh, Léopoldine Lapierre, Fanny Pineau, Fabien Despas

Open access · greenAbstract readReview
In one paragraph

Review in Journal of clinical pharmacy and therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.4field-weighted citation impact, top 4% 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, 48 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Novel Therapeutic Approaches in Pediatric Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2025
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. CD19xCD3 T cell engager shows therapeutic potential for refractory myasthenic syndromes.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  19. Review
  20. Review
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 at 2 institutions in 1 country.

Pauline MocquotDépartement de Pharmacologie Médicale, CHU de Toulouse, Université Toulouse III - Paul Sabatier, Toulouse, France.ORCID https://orcid.org/0000-0001-7181-3525
Yasmine MossazadehDépartement de Pharmacologie Médicale, CHU de Toulouse, Université Toulouse III - Paul Sabatier, Toulouse, France.
Léopoldine LapierreDépartement d'Hématologie et de Médecine Interne, Institut Universitaire du Cancer-Oncopole, CHU de Toulouse, Toulouse, France.
Fanny PineauDépartement d'Hématologie et de Médecine Interne, Institut Universitaire du Cancer-Oncopole, CHU de Toulouse, Toulouse, France.
Fabien DespasDépartement de Pharmacologie Médicale, CHU de Toulouse, Université Toulouse III - Paul Sabatier, Toulouse, France.ORCID https://orcid.org/0000-0002-3116-9963
Université Toulouse III - Paul Sabatier · FRCentre Hospitalier Universitaire de Toulouse · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

WHAT IS KNOWN AND

objectiveBispecific drugs (BDs) belong to the family of immunotherapies along with checkpoint inhibitors and CAR-T cells. In the field of oncology, BDs are designed to simultaneously bind a tumour antigen on the one side and an antigen present on the surface of effector cells on the other. This review summarizes the information available to date on the first marketed BiTE-format bispecific antibody, blinatumomab BLINCYTO® in acute lymphoblastic leukaemia.

methodsA literature search was conducted in the PubMed database by including studies published in English using the term blinatumomab. Furthermore, bibliographies of selected references were also evaluated for relevant articles. Clinical trial (CT) data were retrieved from clinicaltrials.gov (ongoing trials, adverse events [AEs]) and global pharmacovigilance data were retrieved from VigiBase®. RESULTS AND DISCUSSION: Blinatumomab is a fusion protein which consists of two single-chain variable fragments arranged in tandem: the first binds the CD19 surface antigen of all B cells and the second targets the CD3 antigen of T cells. Binding of blinatumomab to B and T cells induces apoptosis of B cells after secretion of granzymes and perforins by T cells. T-cell activation results in secretion of pro-inflammatory cytokines and upregulation of activation markers and adhesion molecules on the surface of T cells. The major CTs that led to an indication show increased overall survival with blinatumomab with better efficacy in patients in haematological remission with minimal residual disease ≥10 WHAT IS NEW AND

conclusionThis review summarizes the current knowledge of blinatumomab in the literature. The subject of many CTs is to improve the route of administration and expand the indications for treatment.

Indexed as

Antibodies, BispecificAntineoplastic AgentsDrug-Related Side Effects and Adverse ReactionsSingle-Chain AntibodiesAntigens, CD19Antigens, NeoplasmCD3 ComplexCytokinesGranzymesHumansAntibodies, BispecificAntigens, CD19Antigens, NeoplasmAntineoplastic AgentsblinatumomabCD3 ComplexCytokinesGranzymesSingle-Chain Antibodiesacute lymphoblastic leukaemiabispecific antibodyblinatumomabpharmacovigilance

Identifiers

PMID35906791
PMCPMC9796714
OpenAlexW4288903796

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.