Literature DB >> 19160429

Antiestrogen therapy for hereditary hemorrhagic telangiectasia: a double-blind placebo-controlled clinical trial.

Eitan Yaniv1, Michal Preis, Tuvia Hadar, Jacob Shvero, Miriam Haddad.   

Abstract

OBJECTIVES/HYPOTHESIS: Hereditary hemorrhagic telangiectasia (HHT) is associated with recurrent epistaxis in 90% of cases. Good response to hormone treatment has been documented, although its use remains controversial. The aim of this study was to examine the efficacy of an antiestrogenic agent, Tamoxifen, in the treatment of HHT-associated epistaxis.
METHODS: Twenty-five patients (11 men, 14 women; mean age 51 years) with a diagnosis of epistaxis due to HHT were randomly assigned to receive treatment with oral tamoxifen 20 mg/d or placebo for 6 months. Follow-up consisted of physical examination and once-monthly blood tests.
RESULTS: The groups were similar in age and sex distribution. Of the 21 participants who completed the trial, alleviation of the epistaxis was noted in 9 of 10 tamoxifen-treated patients and 3 of 11 placebo-treated patients (including 2 with only temporary improvement). The difference between the groups at the trial end point was significant for both frequency (P = .01) and severity (P = .049) of the disease. Hemoglobin concentration rose in 4 tamoxifen-treated patients and decreased in 5 controls.
CONCLUSIONS: Tamoxifen appears to be an effective agent for the treatment of epistaxis due to HHT.

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Year:  2009        PMID: 19160429     DOI: 10.1002/lary.20065

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


  16 in total

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Authors:  Cameron Grigg; Daniel Anderson; James Earnshaw
Journal:  Ochsner J       Date:  2017

2.  Rare manifestations in a case of Osler-Weber-Rendu disease.

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Journal:  BMJ Case Rep       Date:  2015-01-05

3.  A retrospective analysis of low dose, intranasal injected bevacizumab (Avastin) in hereditary haemorrhagic telangiectasia.

Authors:  C Rohrmeier; H G Sachs; T S Kuehnel
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4.  Successful treatment of bleeding gastro-intestinal angiodysplasia in hereditary haemorrhagic telangiectasia with thalidomide.

Authors:  Mohamed Aftab Alam; Sarmad Sami; Sathish Babu
Journal:  BMJ Case Rep       Date:  2011-11-08

5.  Efficacy and safety of thalidomide for the treatment of severe recurrent epistaxis in hereditary haemorrhagic telangiectasia: results of a non-randomised, single-centre, phase 2 study.

Authors:  Rosangela Invernizzi; Federica Quaglia; Catherine Klersy; Fabio Pagella; Federica Ornati; Francesco Chu; Elina Matti; Giuseppe Spinozzi; Sara Plumitallo; Pierangela Grignani; Carla Olivieri; Raffaella Bastia; Francesca Bellistri; Cesare Danesino; Marco Benazzo; Carlo L Balduini
Journal:  Lancet Haematol       Date:  2015-10-27       Impact factor: 18.959

6.  Anti-VEGF with 3-week intervals is effective on anemia in a patient with severe hereditary hemorrhagic telangiectasia.

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Review 7.  Optimal management of hereditary hemorrhagic telangiectasia.

Authors:  Neetika Garg; Monica Khunger; Arjun Gupta; Nilay Kumar
Journal:  J Blood Med       Date:  2014-10-15

8.  Circulatory contributors to the phenotype in hereditary hemorrhagic telangiectasia.

Authors:  Claire L Shovlin
Journal:  Front Genet       Date:  2015-04-09       Impact factor: 4.599

Review 9.  Pericytes as targets in hereditary hemorrhagic telangiectasia.

Authors:  Jérémy Thalgott; Damien Dos-Santos-Luis; Franck Lebrin
Journal:  Front Genet       Date:  2015-02-13       Impact factor: 4.599

10.  Novel Use of Tamoxifen to Reduce Recurrent Gastrointestinal Bleeding in Patients with Left Ventricular Assist Devices.

Authors:  Michael E Plazak; Stephen J Hankinson; Erik N Sorensen; Brent N Reed; Bharath Ravichandran; Van-Khue Ton
Journal:  J Cardiovasc Transl Res       Date:  2020-11-11       Impact factor: 4.132

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