Evidence map›Paper›PMID 25484066›Full record

ArticlemAbs2014

VEGF neutralizing aerosol therapy in primary pulmonary adenocarcinoma with K-ras activating-mutations.

Virginie Hervé, Nathalie Rabbe, Laurent Guilleminault, Flora Paul, Laurène Schlick, Nicolas Azzopardi, Michael Duruisseaux, Delphine Fouquenet, Jérôme Montharu, Françoise Redini and 5 more

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.

  1. FcRn as a Transporter for Nasal Delivery of Biologics: A Systematic Review.International journal of molecular sciences · 2021
    Pooled it
  2. Article
  3. Review
  4. Aerosol pulmonary immune engineering.Advanced drug delivery reviews · 2023
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. 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

15 authors at 10 institutions in 1 country.

Virginie Hervéa Université François Rabelais, UMR , Tours , France.
Nathalie Rabbe
Laurent Guilleminault
Flora Paul
Laurène Schlick
Nicolas Azzopardi
Michael Duruisseaux
Delphine Fouquenet
Jérôme Montharu
Françoise Redini
Gilles Paintaud
Etienne Lemarié
Jacques Cadranel
Marie Wislez
Nathalie Heuzé-Vourc'h
Centre d'Étude des Pathologies RespiratoiresCentre Hospitalier Universitaire de Tours · FRHôpital Tenon · FRInserm · FRUniversité de Tours · FRAssistance Publique – Hôpitaux de Paris · FRCentre National de la Recherche Scientifique · FRClinical Investigation Center Plurithematic Tours · FRTHERANOSCAN : Biomarqueurs Théranostiques des Cancers Bronchiques Non à Petites CellulesUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

K-ras mutations promote angiogenesis in lung cancer and contribute to the drug resistance of cancer cells. It is not clear whether K-ras mutated adenocarcinomas are sensitive to anti-angiogenic therapy with monoclonal antibodies (mAbs) that target vascular endothelial growth factor (VEGF). Anti-angiogenic mAbs are usually delivered systemically, but only a small proportion reaches the lung after intravenous injection. We investigated the relevance of a non-invasive pulmonary route for the delivery of anti-VEGF mAbs in the mouse K-ras(LA1) model. We found that pulmonary delivery of these mAbs significantly reduced the number of tumor lesions and inhibited malignant progression. The antitumor effect involves the VEGFR2-dependent inhibition of blood vessel growth, which impairs tumor proliferation. Pharmacokinetic analysis of aerosolized anti-VEGF showed its low rate of passage into the bloodstream, suggesting that this delivery route is associated with reduced systemic side effects. Our findings highlight the value of the aerosol route for administration of anti-angiogenic mAbs in pulmonary adenocarcinoma with K-ras activating-mutations.

Indexed as

AdenocarcinomaAerosolsAnimalsAntibodies, MonoclonalAntibodies, NeutralizingArea Under CurveBiological AvailabilityBlotting, WesternCell ProliferationCells, CulturedHumansImmunohistochemistryInjections, IntraperitonealLung NeoplasmsMice, Inbred C57BLMice, KnockoutAerosolsAntibodies, MonoclonalAntibodies, NeutralizingHras protein, mouseKdr protein, mouseProto-Oncogene Proteins p21(ras)Vascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2aerosolairways deliveryanti-angiogenic agentanti-VEGFK-ras mutationlung adenocarcinomamonoclonal antibodyNon-small cell lung cancerpharmacokinetics

Identifiers

PMID25484066
PMCPMC4623465
OpenAlexW2110471088

What OpenQuestion holds

Textmetadata
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.