Literature DB >> 29469958

Long-term experience with intranasal bevacizumab therapy.

Johan Steineger1, Terje Osnes1,2, Ketil Heimdal3,4, Sinan Dheyauldeen1.   

Abstract

OBJECTIVES/HYPOTHESIS: Long-term follow-up of intranasal bevacizumab therapy in hereditary hemorrhagic telangiectasia (HHT). STUDY
DESIGN: Prospective, noncomparative study.
METHODS: Patients treated for HHT-associated epistaxis by intranasal submucosal bevacizumab injections between June 2011 and August 2013 were included and followed prospectively. The effectiveness of the treatment was evaluated by the epistaxis severity score (ESS); the epistaxis intensity, frequency, and the need of blood transfusion (IFT) score; and hemoglobin levels.
RESULTS: Thirty-three patients were included. The total number of treatments with intranasal bevacizumab injection was 210. The mean number of treatments per patient was 6.2 ± 4.6 (range, 1-16), and the mean treatment and observation period was 38.8 ± 21.8 months (range, 2-66 months). Four patients showed no improvement after treatment. Eleven patients (33.3%) showed initial improvement in both ESS and IFT, but the treatment was discontinued before the end of the study because the effect became gradually shorter lasting despite repeated injections. Twelve patients (36.3%) continued to have a positive response to the treatment at the end of the study. No local adverse effects were observed, but one patient developed osteonecrosis in both knees during the treatment period.
CONCLUSIONS: Intranasal bevacizumab injection is an effective treatment for most of the moderate and severe grades of HHT-associated epistaxis. The duration of the effect of the treatment was variable. Primary and late resistance phenomena to the treatment were quite common. LEVEL OF EVIDENCE: 4. Laryngoscope, 128:2237-2244, 2018.
© 2018 The American Laryngological, Rhinological and Otological Society, Inc.

Entities:  

Keywords:  Avastin; Epistaxis; bevacizumab; hereditary hemorrhagic telangiectasia; intranasal; long term

Mesh:

Substances:

Year:  2018        PMID: 29469958     DOI: 10.1002/lary.27147

Source DB:  PubMed          Journal:  Laryngoscope        ISSN: 0023-852X            Impact factor:   3.325


  3 in total

1.  Thalidomide for the Management of Bleeding Episodes in Patients with Hereditary Hemorrhagic Telangiectasia: Effects on Epistaxis Severity Score and Quality of Life

Authors:  Mehmet Baysal; Elif G. Ümit; Hakkı Onur Kırkızlar; Ali Caner Özdöver; Ahmet Muzaffer Demir
Journal:  Turk J Haematol       Date:  2018-06-08       Impact factor: 1.831

2.  An in vitro study on the effect of bevacizumab on endothelial cell proliferation and VEGF concentration level in patients with hereditary hemorrhagic telangiectasia.

Authors:  Haneen Sadick; Elena Schäfer; Christel Weiss; Nicole Rotter; Cornelia Emika Müller; Richard Birk; Maliha Sadick; Daniel Häussler
Journal:  Exp Ther Med       Date:  2022-07-05       Impact factor: 2.751

3.  Long-term efficacy assessment of current treatment options for epistaxis in HHT.

Authors:  Cilgia Dür; L Anschuetz; S Negoias; O C Bulut; A Angelillo-Scherrer; M Caversaccio
Journal:  Eur Arch Otorhinolaryngol       Date:  2021-03-04       Impact factor: 2.503

  3 in total

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