Evidence map›Paper›PMID 25751241›Full record

ArticlemAbs2015

Dose - response relationship of bevacizumab in hereditary hemorrhagic telangiectasia.

Nicolas Azzopardi, Sophie Dupuis-Girod, David Ternant, Anne-Emmanuelle Fargeton, Isabelle Ginon, Frédéric Faure, Evelyne Decullier, Adeline Roux, Marie-France Carette, Brigitte Gilbert-Dussardier and 7 more

Open access · goldAbstract read
In one paragraph

Article in mAbs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

10 citing papers in PubMed, 23 citations in OpenAlex.

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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

17 authors at 13 institutions in 5 countries.

Nicolas Azzopardia Université François-Rabelais de Tours ; CNRS, GICC UMR 7292; Tours , France.
Sophie Dupuis-Girod
David Ternant
Anne-Emmanuelle Fargeton
Isabelle Ginon
Frédéric Faure
Evelyne Decullier
Adeline Roux
Marie-France Carette
Brigitte Gilbert-Dussardier
Pierre-Yves Hatron
Pascal Lacombe
Vanessa Leguy-Seguin
Sophie Rivière
Romain Corre
Sabine Bailly
Gilles Paintaud
Hospices Civils de Lyon · FRUniversité de Tours · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Lille · FRCentre Hospitalier Universitaire Dijon Bourgogne · FRCentre Hospitalier Vétérinaire Frégis · FRClinica de Pneumologie Iaşi · ROHôpital Edouard Herriot · FRHôpital Lyon Sud · FRHôpital Tenon · FRLaboratoire de Biophotonique et Pharmacologie · FRLaboratoire de Génétique Cellulaire · FRUniversité Grenoble Alpes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary hemorrhagic telangiectasia (HHT), a genetic vascular disorder associated with epistaxis and hepatic shunts, is responsible for high-output cardiac failure in rare cases. Bevacizumab, which targets vascular endothelial growth factor, was shown to decrease both cardiac index (CI) and epistaxis duration in HHT patients with severe liver involvement. The relationship between its serum concentration and change in both CI and epistaxis duration was investigated to design the bevacizumab maintenance dosing regimen of future therapeutic studies. Twenty-five HHT patients with dyspnea and high CI were included in a prospective non-comparative study. They received bevacizumab at a dose of 5 mg/kg per infusion every 14 days for a total of 6 injections. The relationships between bevacizumab serum concentration and both CI and epistaxis duration were described using transit compartments and direct inhibition pharmacokinetic-pharmacodynamic models. The performances of different maintenance regimens were evaluated using simulation. Infusions every 3, 2 and one months were predicted to maintain 41%, 45% and 50% of patients with CI <4 L/min/m(2) at 24 months, respectively. The fraction of patients with <20 min epistaxis per month was predicted to be 34%, 43% and 60%, with infusion every 3, 2 or one months, respectively. Simulations of the effects of different maintenance dosing regimens predict that monthly 5 mg/kg infusions of bevacizumab should allow sustained control of both cardiac index and epistaxis.

Indexed as

Angiogenesis InhibitorsBevacizumabModels, BiologicalAdultAgedDose-Response Relationship, DrugFemaleHumansMaleMiddle AgedProspective StudiesTelangiectasia, Hereditary HemorrhagicAngiogenesis InhibitorsBevacizumabangiogenesis factorsangiogenicantiangiogenesis agentsAUC, area under the concentration vs time curveAVM, arterovenous malformationsbevacizumabCI, cardiac indexdose-response relationshipELISA, enzyme-linked immunosorbent assayhereditary hemorrhagic telangiectasiaHHT, hereditary hemorrhagic telangectasiaIgG, immunoglobulin GIIV, interindividual variabilitypharmacokineticsPK-PD, pharmacokinetic-pharmacodynamicTGF-β, transforming growth factor βTMDD, target-mediated drug dispositionVEGF, vascular endothelial growth factor

Identifiers

PMID25751241
PMCPMC4622710
OpenAlexW1512570069

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.