Evidence map›Paper›PMID 40290758›Full record

ArticleTherapeutic advances in hematology2025

BEST study: one-year descriptive follow-up of bevacizumab treatment in hereditary haemorrhagic telangiectasia post-BABH interventional study.

Sophie Dupuis-Girod, Evelyne Decullier, Sophie Rivière, Christian Lavigne, Vincent Grobost, Vanessa Leguy-Seguin, Hélène Maillard, Thierry Chinet, Anne-Emmanuelle Fargeton, Alexandre Guilhem and 1 more

Registry-linked trialAbstract read
In one paragraph

Article in Therapeutic advances in hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06039124 (Subsequent Bevacizumab Treatment in Patients With HHT After the End of BABH Interventional Study. A Descriptive Study.), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT06039124 completednot on this map

Subsequent Bevacizumab Treatment in Patients With HHT After the End of BABH Interventional Study. A Descriptive Study.

TypeobservationalSponsorHospices Civils de LyonRan2021 to 2022Enrolled23ConditionsHemorrhagic Hereditary Telangiectasia, HHTArmsbevacizumab treatment
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

11 authors.

Sophie Dupuis-GirodHospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et centre de Référence de la maladie de Rendu-Osler, 59 Bd Pinel, Bron 69677, France.ORCID https://orcid.org/0000-0002-8834-5526
Evelyne DecullierHospices Civils de Lyon, Pôle Santé Publique, Lyon, France.
Sophie RivièreService de Médecine Interne A, Centre Hospitalier Universitaire, Montpellier, France.
Christian LavigneService de médecine interne-Immunologie clinique, CHU d'Angers, Angers Cedex 09, France.
Vincent GrobostService de Médecine Interne CHU Estaing, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Vanessa Leguy-SeguinService de Médecine Interne 1, CHU Francois Mitterrand, Dijon, France.
Hélène MaillardService de Médecine Interne et Immunologie Clinique, CHU Lille, Lille, France.
Thierry ChinetCentre Rendu-Osler, Hôpital Ambroise Paré, Assistance Publique-Hôpitaux de Paris, Université de Versailles SQY, Boulogne, France.
Anne-Emmanuelle FargetonHospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Centre de Référence de la maladie de Rendu-Osler, Bron, France.
Alexandre GuilhemHospices Civils de Lyon, Hôpital Femme-Mère-Enfants, Service de Génétique et centre de Référence de la maladie de Rendu-Osler, Bron, France.
Ruben HermannHospices Civils de Lyon, Hôpital, Service d'ORL, Hôpital E. Herriot, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hereditary haemorrhagic telangiectasia (HHT) is a genetic vascular disorder characterised by telangiectases, which cause nasal and gastrointestinal (GI) bleeding, and visceral arteriovenous malformations. Since 2012 bevacizumab, a monoclonal antibody targeting vascular endothelial growth factor, has been a promising treatment for HHT-related bleeding and was evaluated in the phase II BABH study. Objective: To follow and describe evolution and treatments of patients with HHT post-BABH study. Design: This study is a 1-year, multi-centre descriptive study. Methods: We collected clinical (nose and GI bleeding, red blood cell transfusions) and biological (haemoglobin and ferritin levels) data and treatment information. Results: Of 22 patients included across 4 centers, 15 received bevacizumab. Among them, 12 (86%) had a >50% decrease in the number of RBC units transfused 3 months post-treatment. Mean haemoglobin levels increased from 83.08 to 105.98 g/L. Conclusion: Bevacizumab effectively reduces RBC transfusions and is efficient for treating severe bleeding in patients with HHT. Trial registration: This trial was registered with the ClinicalTrials.gov Identifier #NCT06039124.

Indexed as

bevacizumabhereditary haemorrhagic telangiectasiarare vascular diseasered blood cell transfusion

Identifiers

PMID40290758
PMCPMC12033602

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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.