The Role of Thalidomide and Its Analogs in the Treatment of Hereditary Hemorrhagic Telangiectasia: A Systematic Review

被引:1
作者
Ugur, Mehmet Can [1 ]
Baysal, Mehmet [2 ]
Umit, Elif Gulsum [3 ]
机构
[1] Izmir Bakircay Univ, Cigli Training & Res Hosp, Dept Internal Med, Div Hematol, TR-35665 Izmir, Turkiye
[2] Ali Osman Sonmez Oncol Hosp, Div Hematol, TR-16040 Bursa, Turkiye
[3] Trakya Univ, Fac Med, Dept Internal Med, Div Hematol, TR-22030 Edirne, Turkiye
关键词
hereditary hemorrhagic telangiectasia (HHT); thalidomide; pomalidomide; lenalidomide; Osler-Weber-Rendu; GASTROINTESTINAL ANGIODYSPLASIA; EPISTAXIS; MANAGEMENT; DIAGNOSIS; LENALIDOMIDE; GUIDELINES; THERAPY;
D O I
10.3390/jcm13185404
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Hereditary hemorrhagic telangiectasia (HHT) is a disease characterized by arteriovenous malformations and telangiectases, in which the endothelium and immune system play a role in the pathophysiology. Therefore, treatments with antiangiogenic properties which are also regarded as immunomodulators were demonstrated to play an important role in treatment. This systematic review aimed to gather the accumulated information of the use of thalidomide and its analogs in the treatment of HHT. Methods: In this systematic review, publications that were published up to March 2024 and met the inclusion criteria were compiled using the keywords 'thalidomide', 'lenalidomide', 'pomalidomide', 'immunomodulatory drugs' and 'HHT' in Medline and Scholars databases. Results: A total of 53 articles were evaluated and 15 were included in the study. Thalidomide was the predominant used agent and was observed to be used in patients with ages ranging from 37 to 77 years, with doses ranging from 50 to 200 mg daily, and the mean follow-up period was observed to be 6-60 months. Assessments regarding efficacy were based on the epistaxis severity score (ESS), hemoglobin level, and transfusion independence. While thalidomide showed significant efficacy, it also had an adverse event rate of any severity of up to 85% of patients. Use of lenalidomide to control bleeding in HHT was reported in a single case report, while the use of pomalidomide was observed to be investigated in Phase 1 and Phase 2 studies in patients aged 48 to 70 years, with doses ranging from 1 to 5 mg daily for 6-24 months. This treatment was reported to provide significant improvement in hemoglobin levels and ESS. Adverse events of any severity were observed at a frequency of 60-66%. Conclusions: Antiangiogenic agents such as thalidomide, lenalidomide, and pomalidomide may be effective in managing HHT. However, further studies are needed to optimize the timing, dose, and sequence.
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页数:11
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