Evidence map›Paper›PMID 19304016›Full record

ReviewLancet (London, England)2009

Monoclonal antibodies for cancer immunotherapy.

Louis M Weiner, Madhav V Dhodapkar, Soldano Ferrone

Registry-linked trialOpen access · greenAbstract readReview
In one paragraph

Review in Lancet (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02914405 (A Phase I Study of 131-1 mIBG Followed by Nivolumab and Dinutuximab Beta in Children With Relapsed/Refractory Neuroblastoma), which is not on this map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
22.0field-weighted citation impact, top 1% 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.

NCT02914405 phase1active not recruitingnot on this mapstarted 2018, after this paper: background citation

A Phase I Study of 131-1 mIBG Followed by Nivolumab and Dinutuximab Beta in Children With Relapsed/Refractory Neuroblastoma

TypeinterventionalSponsorUniversity Hospital Southampton NHS Foundation TrustRan2018 to 2026Enrolled44ConditionsNeuroblastomaArmsNivolumab, Ch14.18/CHO
3 · Its place in the literature

Who cites it

129 citing papers in PubMed, 304 citations in OpenAlex.

  1. Trial
  2. Review
  3. Embracing cancer immunotherapy with manganese particles.Cellular oncology (Dordrecht, Netherlands) · 2025
    Review
  4. Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Therapeutic applications of nanobiotechnology.Journal of nanobiotechnology · 2023
    Review
  17. Review
  18. Review
  19. Article
  20. Article

69 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 1 country.

Louis M WeinerLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.
Madhav V Dhodapkar
Soldano Ferrone
Georgetown University · USUPMC Hillman Cancer Center · USYale University · US

Funding

Tissue Culture Shared ResourceP30CA051008 · NCI · GEORGETOWN UNIVERSITY · PI STEPHEN W BYERS · 1990 to 2026
$71.5M
TARGETED IMMUNOTHERAPY USING BISPECIFIC ANTIBODIESR01CA050633 · NCI · GEORGETOWN UNIVERSITY · PI WEINER, LOUIS M. · 1989 to 2018
$6.5M
Anti-Tumor immunity in myelomaR01CA106802 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2004 to 2016
$3.3M
Rational Design of HMW-MAA Peptide MimicsR01CA105500 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FERRONE, SOLDANO · 2004 to 2008
$1.6M
Targeting myeloma via dendritic cellsR01CA109465 · NCI · YALE UNIVERSITY · PI DHODAPKAR, MADHAV V · 2005 to 2009
$1.6M
Adaptive Immunity from High Affinity Anti-HER2/neu Monoclonal AntibodiesR01CA121033 · NCI · GEORGETOWN UNIVERSITY · PI WEINER, LOUIS M. · 2006 to 2010
$1.5M
NCI NIH HHS P30 CA051008NCI NIH HHS R01 CA050633NCI NIH HHS R01 CA105500NCI NIH HHS R01 CA106802NCI NIH HHS R01 CA109465NCI NIH HHS R01 CA121033
6 · The paper itself

Abstract

Monoclonal antibodies are effective treatments for many malignant diseases. However, the ability of antibodies to initiate tumour-antigen-specific immune responses has received less attention than have other mechanisms of antibody action. We describe the rationale and evidence for the development of antibodies that can stimulate host tumour-antigen-specific immune responses. Such responses can be induced through the induction of antibody-dependent cellular cytotoxicity, promotion of antibody-targeted cross-presentation of tumour antigens, or by triggering of the idiotypic network. Future treatment modifications or combinations might be able to prolong, amplify, and shape these immune responses to increase the clinical benefits of antibody therapy for human cancer.

Indexed as

Antibodies, Anti-IdiotypicAntibodies, MonoclonalAntigen PresentationAntigens, NeoplasmCancer VaccinesHumansImmunotherapyNeoplasmsAntibodies, Anti-IdiotypicAntibodies, MonoclonalAntigens, NeoplasmCancer Vaccines

Identifiers

PMID19304016
PMCPMC2677705
OpenAlexW2122584026

What OpenQuestion holds

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Registered trials

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.