Evidence map›Paper›PMID 22833213›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2012

A comparative study of PDGFR inhibition with imatinib on radiolabeled antibody targeting and clearance in two pathologically distinct models of colon adenocarcinoma.

Vineeth S Rajkumar, Geoff Boxer, Mathew Robson, John Muddle, Yanni Papastavrou, R Barbara Pedley

Abstract read
PubMed Publisher
In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
1.3field-weighted citation impact, top 21% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Association between IRS-1 Gly972Arg polymorphism and colorectal cancer risk.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  2. Association between IL-4 -589C>T polymorphism and colorectal cancer risk.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Targeting platelet-derived growth factor (PDGF) signaling in gastrointestinal cancers: preclinical and clinical considerations.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Review
  9. Emerging trends for radioimmunotherapy in solid tumors.Cancer biotherapy & radiopharmaceuticals · 2013
    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

6 authors at 4 institutions in 2 countries.

Vineeth S RajkumarDepartment of Oncology, UCL Cancer Institute, Paul O'Gorman Building, University College London, London WC1 6BT, UK. v.rajkumar@ucl.ac.uk
Geoff Boxer
Mathew Robson
John Muddle
Yanni Papastavrou
R Barbara Pedley
UCL Australia · AUUniversity College London · GBCRUK Lung Cancer Centre of Excellence · GBMiddlesex University · GB

Funding

Cancer Research UKDepartment of HealthMedical Research Council G1001497
6 · The paper itself

Abstract

The potential of radioimmunotherapy to selectively kill tumour cells is well established. However, optimisation is required with regards to increasing tumour localisation of antibodies. We used the PDGF-receptor inhibitor imatinib mesylate to improve tumour-specific antibody localisation in two models of colorectal adenocarcinoma and correlated antibody localisation with changes to tumour microvasculature. Mice bearing human colorectal xenografts (LS174T or SW1222) were treated with imatinib prior to administration of radiolabeled anti-CEA antibodies ((125)I-A5B7). Whole tumour and regional localisation of radiolabeled antibodies were measured. Microvessel density and pericyte coverage were quantified in whole tumours and correlated with (125)I-A5B7 localisation. Imatinib increased uptake of (125)I-A5B7 in LS174T but not SW1222 tumours after 48 h (p < 0.05). Imatinib reduced microvessel density in both models (p < 0.05) but reduced pericyte attachment to endothelial cells only in SW1222 xenografts (p < 0.05). Imatinib increases antibody distribution in LS174T tumours but not SW1222 tumours, and this correlated to changes in tumour microvessels. Accelerated clearance of radiolabeled antibody from normal tissues in both models resulted in enhanced tumour to normal tissue ratios. This improvement in tumour/normal tissue ratio has potential clinical benefit from a therapy and imaging perspective, and merits further investigation.

Indexed as

Disease Models, AnimalRadioimmunotherapyAdenocarcinomaAnimalsAntibodies, MonoclonalAntineoplastic AgentsBenzamidesCarcinoembryonic AntigenColorectal NeoplasmsCombined Modality TherapyFemaleFluorescent Antibody TechniqueHumansImatinib MesylateImmunoenzyme TechniquesMiceAntibodies, MonoclonalAntineoplastic AgentsBenzamidesCarcinoembryonic AntigenImatinib MesylatePiperazinesPyrimidinesReceptor, Platelet-Derived Growth Factor beta

Identifiers

PMID22833213
OpenAlexW1991456902

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.