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

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.

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Publication Details

Journal
Angiogenesis
Published
2024-12-24
DOI
https://doi.org/10.1007/s10456-024-09962-4
Citations
7
Primary Topic
Vascular Anomalies and Treatments
Type
article
Field-Weighted Citation Impact
3.07

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article

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

Caroline Gervaise, Sophie Dupuis‐Girod, Xavier Dufour, Adeline Roux et al.
7 citations
Angiogenesis
Vascular Anomalies and Treatments
3.07
article

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

Caroline Gervaise, Sophie Dupuis‐Girod, Xavier Dufour, Adeline Roux, Sophie Rivière, Ruben Hermann, Laurent Laccourreye, F. Jegoux, Margaux Grall, N. Saroul, Isabelle Wagner, M. Kerjouan, Évelyne Decullier, Anne‐Emmanuelle Fargeton, Christian Lavigne, Vincent Grobost, J. Séguier, Antoine Parrot, C. Cartier, Justin Michel, Margaux Huot, Xavier Le-Guillou, Aurélie de-Montigny
article en
7 citations

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.

AngiogenesisVol. 28(1)
Inserm (FR), Aix-Marseille Université (FR), Université de Poitiers (FR), Sorbonne Université (FR), Hôpital Femme Mère Enfant (FR), Centre Hospitalier Universitaire de Montpellier (FR), Assistance Publique – Hôpitaux de Paris (FR), Hospices Civils de Lyon (FR), Centre Hospitalier Universitaire de Poitiers (FR), Centre Hospitalier Universitaire d'Angers (FR), Hôpital Edouard Herriot (FR), Centre Hospitalier Universitaire de Clermont-Ferrand (FR), Institut Universitaire des Systèmes Thermiques Industriels (FR), Hôpital Saint Eloi (FR), Centre Hospitalier Universitaire de Rennes (FR), Hôpital de la Timone (FR), Hôpital Tenon (FR), Université d'Angers (FR)
Hospices Civils de Lyon
Good health and well-being
Openalex Percentile: Top 8%
Vascular Anomalies and Treatments
3.07
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