Evidence map›Paper›PMID 20521223›Full record

ReviewCurrent opinion in molecular therapeutics2010

Cancer therapy with bispecific antibodies: Clinical experience.

Archana Thakur, Lawrence G Lum

Abstract readReview
In one paragraph

Review in Current opinion in molecular therapeutics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.5field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 62 citations in OpenAlex.

  1. Review
  2. Review
  3. DNA-Mediated Assembly of Multispecific Antibodies for T Cell Engaging and Tumor Killing.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2020
    Article
  4. Article
  5. Bispecific antibodies in cancer immunotherapy.Therapeutic advances in vaccines and immunotherapy · 2018
    Review
  6. Article
  7. Review
  8. Article
  9. Generation of MANAbodies specific to HLA-restricted epitopes encoded by somatically mutated genes.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  10. Synthetic biology approaches to engineer T cells.Current opinion in immunology · 2015
    Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Cytokine-induced killer cells promote antitumor immunity.Journal of translational medicine · 2013
    Review
  20. Article
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

2 authors at 1 institution in 1 country.

Archana ThakurBarbara Ann Karmanos Cancer Institute, Wayne State University, Department of Medicine, Detroit, MI 48201, USA.
Lawrence G Lum
The Barbara Ann Karmanos Cancer Institute · US

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI PAUL M STEMMER · 1985 to 2026
$68.4M
Breast Cancer Treatment with Antibody Targeted T CellsR01CA092344 · NCI · WAYNE STATE UNIVERSITY · PI LUM, LAWRENCE G · 2002 to 2012
$4.6M
NCI NIH HHS 5P30CA022453-24NCI NIH HHS P30 CA022453NCI NIH HHS R01 CA092344
6 · The paper itself

Abstract

The binding of at least two molecular targets simultaneously with a single bispecific antibody is an attractive concept. The use of bispecific antibodies as possible therapeutic agents for cancer treatment was proposed in the mid-1980s. The design and production of bispecific antibodies using antibody- and/or receptor-based platform technology has improved significantly with advances in the knowledge of molecular manipulations, protein engineering techniques, and the expression of antigens and receptors on healthy and malignant cells. The common strategy for making bispecific antibodies involves combining the variable domains of the desired mAbs into a single bispecific structure. Many different formats of bispecific antibodies have been generated within the research field of bispecific immunotherapeutics, including the chemical heteroconjugation of two complete molecules or fragments of mAbs, quadromas, F(ab')2, diabodies, tandem diabodies and single-chain antibodies. This review describes key modifications in the development of bispecific antibodies that can improve their efficacy and stability, and provides a clinical perspective on the application of bispecific antibodies for the treatment of solid and liquid tumors, including the promises and research limitations of this approach.

Indexed as

Antibodies, BispecificNeoplasmsAntibodies, MonoclonalHumansProtein EngineeringSingle-Chain AntibodiesAntibodies, BispecificAntibodies, MonoclonalSingle-Chain Antibodies

Identifiers

PMID20521223
PMCPMC3785321
OpenAlexW1513884174

What OpenQuestion holds

Textmetadata
LicenceTDM
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.