Evidence map›Paper›PMID 39718659›Full record

Trial reportAngiogenesis2024

Effect of oral nintedanib vs placebo on epistaxis in hereditary hemorrhagic telangiectasia: the EPICURE multicenter randomized double-blind trial.

Ruben Hermann, Vincent Grobost, Xavier Le-Guillou, Christian Lavigne, Antoine Parrot, Sophie Rivière, Julie Séguier, Anne-Emmanuelle Fargeton, Aurélie de-Montigny, Margaux Huot and 13 more

Registry-linked trialAbstract readRandomized Controlled TrialMulticenter StudyClinical Trial, Phase II
In one paragraph

Trial report in Angiogenesis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03954782 (Efficacy of Nintedanib Per os as a Treatment for Epistaxis in HHT Disease. A National, Randomized, Multicentre Phase II Study), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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.

NCT03954782 phase2completednot on this map

Efficacy of Nintedanib Per os as a Treatment for Epistaxis in HHT Disease. A National, Randomized, Multicentre Phase II Study

TypeinterventionalSponsorHospices Civils de LyonRan2020 to 2023Enrolled61ConditionsTelangiectasia, Hereditary Hemorrhagic, Rendu Osler DiseaseArmsNintedanib 150 mg and 100 mg soft capsules, Oral treatment of placebo soft capsule
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

23 authors.

Ruben HermannService d'ORL, chirurgie cervico-faciale et d'audiophonologie, Hôpital Edouard Herriot, Hospices Civils de Lyon, 5 Place d'Arsonval, 69003, Lyon, France. ruben.hermann@chu-lyon.fr.
Vincent GrobostService de Médecine Interne, CHU Estaing, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Xavier Le-GuillouMedical Genetics Department, University Hospital of Poitiers, 86000, Poitiers, France.
Christian LavigneDepartment of Internal Medicine and Clinical Immunology, Angers University Hospital, Angers, France.
Antoine ParrotAssistance Publique-Hôpitaux de Paris, Service de Pneumologie et Centre de Compétence de la Maladie de Rendu Osler, Hôpital Tenon, 75020, Paris, France.
Sophie RivièreService de Médecine Interne A, Centre Hospitalier Universitaire, Montpellier, France.
Julie SéguierAix-Marseille Univ, APHM, Médecine Interne, Hôpital de la Timone, Marseille, France.
Anne-Emmanuelle FargetonService de Génétique et centre de reference de la maladie de Rendu-Osler, Hôpital Femme-Mère-Enfants, Hospices Civils de Lyon, Bron, France.
Aurélie de-MontignyService de Biostatistique et Bioinformatique des HCL, Lyon, France.
Margaux HuotService de Biostatistique et Bioinformatique des HCL, Lyon, France.
Evelyne DecullierPôle Santé Publique, Hospices Civils de Lyon, Lyon, France.
Adeline RouxPôle Santé Publique, Hospices Civils de Lyon, Lyon, France.
Caroline GervaiseService de pharmaceutique, Groupement Hospitalier Est, Hospices Civils de Lyon, Bron, France.
César CartierService d'ORL Centre Hospitalier Universitaire, Montpellier, France.
Xavier DufourService de Chirurgie ORL, Centre Hospitalier Universitaire de Poitiers, Poitiers, France.
Margaux GrallService d'ORL, chirurgie cervico-faciale et d'audiophonologie, Hôpital Edouard Herriot, Hospices Civils de Lyon, 5 Place d'Arsonval, 69003, Lyon, France.
Frank JegouxService de Chirurgie ORL, Centre Hospitalier Universitaire Pontchaillou, Rennes, France.
Laurent LaccourreyeService d'ORL, CHU d'Angers, Angers cedex 9, France.
Justin MichelDepartment of Otorhinolaryngology-Head and Neck Surgery, Aix Marseille University, 36900APHM, IUSTI, La Conception University Hospital, Marseille, France.
Nicolas SaroulService d'ORL, Hôpital Gabriel Montpied, CHU Clermont Ferrand, Clermont-Ferrand, France.
Isabelle WagnerDepartment of Otorhinolaryngology-Head and Neck Surgery, Sorbonne University, Tenon Hospital, AP-HP, Paris, France.
Mallorie KerjouanService de Pneumologie, CHU Rennes, Rennes, France.
Sophie Dupuis-GirodService de Génétique et centre de reference de la maladie de Rendu-Osler, Hôpital Femme-Mère-Enfants, Hospices Civils de Lyon, Bron, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epistaxis greatly affects patients with hereditary hemorrhagic telangiectasia (HHT). Although few systemic treatment exist, nintedanib, is a good candidate thanks to its anti-angiogenic activity. Our main objective was to evaluate the efficacy of oral nintedanib on epistaxis duration in HHT patients with moderate to severe epistaxis. This multicenter phase 2 randomized, placebo-controlled, double-blind trial was conducted between June 2020 and February 2023. Inclusion criteria were being over 18 years old and having a confirmed HHT diagnosis with an epistaxis severity score greater than 4. Sixty patients were randomized to receive either nintedanib or placebo for 12 weeks with a 12 week follow-up. The primary endpoint was the proportion of patients achieving a reduction of at least 50% in mean monthly epistaxis duration comparing the 8 weeks before treatment to the last 8 weeks of treatment. Main secondary outcomes included monthly duration and frequency of epistaxis and hemoglobin levels. Of the 60 randomized patients, 56 completed the trial. Thirteen patients (43%) in the nintedanib group vs 8 (27%) in the placebo group met the primary endpoint (p = 0.28). We observed a significant decrease in median epistaxis (57% vs 27%, p = 0.013) and a significant increase in median hemoglobin levels (+ 18 vs - 1 g/L, p = 0.02) in the nintedanib vs the placebo group. Although we did not achieve our primary outcome, we observed a significant reduction in epistaxis duration and a significant increase in hemoglobin levels in patients treated with nintedanib. This supports the efficacy of nintedanib, and further studies are needed.

Indexed as

EpistaxisIndolesTelangiectasia, Hereditary HemorrhagicAdministration, OralAdultAgedAngiogenesis InhibitorsDouble-Blind MethodFemaleHumansMaleMiddle AgedTreatment OutcomeAngiogenesis InhibitorsIndolesnintedanibAnemiaAnti-angiogenicEpistaxisHereditary hemorrhagic telangiectasiaNintedanibTyrosine kinase inhibitors

Identifiers

PMID39718659
PMCPMC11668894

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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.