Evidence map›Paper›PMID 27575850›Full record

ArticleBritish journal of cancer2016

A functional bioassay to determine the activity of anti-VEGF antibody therapy in blood of patients with cancer.

Madelon Q Wentink, Henk J Broxterman, Siu W Lam, Epie Boven, Maudy Walraven, Arjan W Griffioen, Roberto Pili, Hans J van der Vliet, Tanja D de Gruijl, Henk M W Verheul

Open access · hybridAbstract read
In one paragraph

Article in British journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact, top 94% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

10 authors at 3 institutions in 2 countries.

Madelon Q WentinkDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Henk J BroxtermanDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Siu W LamDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Epie BovenDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Maudy WalravenDepartment of Medical Oncology, University Medical Center, Utrecht, The Netherlands.
Arjan W GriffioenDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Roberto PiliDepartment of Hematology/Oncology, Indiana University, Indianapolis, Indiana.
Hans J van der VlietDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Tanja D de GruijlDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Henk M W VerheulDepartment of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Amsterdam UMC Location VUmc · NLIndiana University – Purdue University Indianapolis · USUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOnly a small proportion of patients respond to anti-VEGF therapy, pressing the need for a reliable biomarker that can identify patients who will benefit. We studied the biological activity of anti-VEGF antibodies in patients' blood during anti-VEGF therapy by using the Ba/F3-VEGFR2 cell line, which is dependent on VEGF for its growth.

methodsSerum samples from 22 patients with cancer before and during treatment with bevacizumab were tested for their effect on proliferation of Ba/F3-VEGFR2 cells. Vascular endothelial growth factor as well as bevacizumab concentrations in serum samples from these patients were determined by enzyme linked immunosorbent assay (ELISA).

resultsThe hVEGF-driven cell proliferation was effectively blocked by bevacizumab (IC

conclusionsWe found that the neutralising effect of anti-VEGF antibody therapy on the biological activity of circulating VEGF can be accurately determined with a Ba/F3-VEGFR2 bioassay. The value of this bioassay to predict clinical benefit of anti-VEGF antibody therapy needs further clinical evaluation in a larger randomised cohort.

Indexed as

Biological AssayEnzyme-Linked Immunosorbent AssayAngiogenesis InhibitorsAnimalsBevacizumabB-LymphocytesCell DivisionCell LineInterleukin-3MiceNeoplasmsReceptors, ErythropoietinReceptors, Interleukin-3Recombinant Fusion ProteinsReproducibility of ResultsVascular Endothelial Growth Factor AAngiogenesis InhibitorsBevacizumabInterleukin-3KDR protein, humanKdr protein, mouseReceptors, ErythropoietinReceptors, Interleukin-3Recombinant Fusion ProteinsVascular Endothelial Growth Factor AVascular Endothelial Growth Factor Receptor-2VEGFA protein, human

Identifiers

PMID27575850
PMCPMC5061906
OpenAlexW2513929170

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Registered trials

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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.