Literature DB >> 23485837

Systemic therapy with bevacizumab in patients with hereditary hemorrhagic telangiectasia (HHT).

Ajay Chavan1, Silke Schumann-Binarsch, Lars Luthe, Britta Nickau, Albrecht Elsässer, Thomas Kühnel, Urban Geisthoff, Henning Köhne.   

Abstract

BACKGROUND: Frequent epistaxis, the hallmark of hereditary hemorrhagic telangiectasia (HHT) significantly affects quality of life. Hepatic involvement may be associated with capsular pain, abdominal angina, high-output cardiac failure and portal hypertension with ascites and variceal bleeding. Liver transplantation as well as hepatic artery embolization as invasive treatment options for hepatic involvement are both associated with a certain morbidity and mortality. PATIENTS AND METHODS: Three patients with HHT and symptomatic hepatic involvement prospectively underwent off-label systemic treatment with the vascular endothelial growth factor (VEGF)-inhibitor bevacizumab in 6 cycles. Clinical symptoms and cardiac output were assessed before as well as 3 months after therapy.
RESULTS: At 3 months follow-up, capsular pain and abdominal angina were significantly reduced in two of the three patients (Numerical Rating Scale (NRS) grade 4 and 5 changed to grade 2). Cardiac output, which was initially raised in both patients, normalized and was associated with an improvement in the signs and symptoms of cardiac insufficiency by one stage according to the NYHA classification in both patients. Symptoms however returned back gradually to pre-therapeutic levels after 9 months in one of these two patients. In the third patient with a normal cardiac status prior to therapy, a marked subjective improvement in the performance status, fatigability and quality of life was noted. Grade 2 nasal bleeding reduced to grade 0 - 1 in all three patients; this clinical improvement was persistent at 3, 7 and 9 months follow-up. No significant lasting complications were observed.
CONCLUSIONS: Sytemic bevacizumab therapy could become an important therapy option in the non-invasive medical treatment of patients with HHT. Further studies to document long-term results, to determine the appropriate drug dosage as well as to evaluate the necessity of a maintenance drug regime are warranted.

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Year:  2013        PMID: 23485837     DOI: 10.1024/0301-1526/a000253

Source DB:  PubMed          Journal:  Vasa        ISSN: 0301-1526            Impact factor:   1.961


  7 in total

1.  Influence of temporary nasal occlusion (tNO) on epistaxis frequency in patients with hereditary hemorrhagic telangiectasia (HHT).

Authors:  Kornelia E C Wirsching; Frank Haubner; Thomas S Kühnel
Journal:  Eur Arch Otorhinolaryngol       Date:  2017-01-09       Impact factor: 2.503

2.  Bevacizumab: an option for refractory epistaxis in hereditary haemorrhagic telangiectasia.

Authors:  Arno Amann; Normann Steiner; Eberhard Gunsilius
Journal:  Wien Klin Wochenschr       Date:  2015-05-19       Impact factor: 1.704

3.  Successful management of chronic gastrointestinal hemorrhage using bevacizumab in the setting of hereditary hemorrhagic telangiectasia.

Authors:  Mary E Sehl; Theresa M Gruber; Justin P McWilliams; Victor J Marder
Journal:  Am J Hematol       Date:  2015-05-10       Impact factor: 10.047

4.  Clinical Assessment and Lesion-Specific Management of Orbital Vascular Malformations.

Authors:  Daniel B Rootman; Stefania B Diniz; Liza M Cohen
Journal:  J Neurol Surg B Skull Base       Date:  2021-03-23

5.  Development of a 3D angiogenesis model to study tumour - endothelial cell interactions and the effects of anti-angiogenic drugs.

Authors:  Arno Amann; Marit Zwierzina; Stefan Koeck; Gabriele Gamerith; Elisabeth Pechriggl; Julia M Huber; Edith Lorenz; Jens M Kelm; Wolfgang Hilbe; Heinz Zwierzina; Johann Kern
Journal:  Sci Rep       Date:  2017-06-07       Impact factor: 4.379

6.  The effects of nasal closure on quality of life in patients with hereditary hemorrhagic telangiectasia.

Authors:  Rhett S Thomson; Nicole L Molin; Kevin J Whitehead; Shaelene Ashby; Leland Johnson; P Daniel Ward; Bryan R McRae; Kevin F Wilson; Jamie McDonald
Journal:  Laryngoscope Investig Otolaryngol       Date:  2018-04-19

7.  Bevacizumab to Treat Cholangiopathy in Hereditary Hemorrhagic Telangiectasia: Be Cautious: A Case Report.

Authors:  Quentin Maestraggi; Mohamed Bouattour; Ségolène Toquet; Roland Jaussaud; Reza Kianmanesh; François Durand; Amélie Servettaz
Journal:  Medicine (Baltimore)       Date:  2015-11       Impact factor: 1.817

  7 in total

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