Long-term safety and efficacy of subcutaneous C1-inhibitor in older patients with hereditary angioedema

被引:5
|
作者
Bernstein, Jonathan A. [1 ,2 ]
Schwartz, Lawrence [3 ]
Yang, William [4 ,5 ]
Baker, James [6 ]
Anderson, John [7 ]
Farkas, Henriette [8 ]
Aygoeren-Puersuen, Emel [9 ]
Bygum, Anette [10 ,11 ]
Jacobs, Iris [12 ]
Feuersenger, Henrike [13 ]
Pragst, Ingo [13 ]
Riedl, Marc A. [14 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Internal Med, Allergy Sect,Div Immunol, 231 Albert Sabin Way ML 563, Cincinnati, OH 45267 USA
[2] Bernstein Clin Res Ctr, Cincinnati, OH USA
[3] Virginia Commonwealth Univ, Dept Internal Med, Richmond, VA USA
[4] Ottawa Allergy Res Corp, Ottawa, ON, Canada
[5] Univ Ottawa, Med Sch, Ottawa, ON, Canada
[6] Baker Allergy Asthma & Dermatol Res Ctr, Portland, OR USA
[7] Clin Res Ctr Alabama, Birmingham, AL USA
[8] Semmelweis Univ, Hungarian Angioedema Reference Ctr, Dept Internal Med 3, Budapest, Hungary
[9] Klinikum Johann Wolfgang Goethe Univ, Klin Kinder & Jugendmed, Frankfurt, Germany
[10] Odense Univ Hosp, Hereditary Angioedema Ctr Denmark, Dept Dermatol, Odense, Denmark
[11] Odense Univ Hosp, Allergy Ctr, Odense, Denmark
[12] CSL Behring, King Of Prussia, PA USA
[13] CSL Behring, Marburg, Germany
[14] Univ Calif San Diego, San Diego Sch Med, La Jolla, CA 92093 USA
关键词
ATTACKS; MANAGEMENT; SYMPTOMS; DEFICIENCY; RISK; AGE;
D O I
10.1016/j.anai.2020.05.015
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background: Patients aged 65 years and older with hereditary angioedema (HAE) owing to C1-inhibitor (C1-INH) deficiency may have an altered response to treatment and are at higher risk for treatment-related adverse events (AEs) because of comorbidities and polypharmacy. Objective: To investigate the safety and efficacy of subcutaneous C1 esterase inhibitor (C1-INH) in patients aged 65 years and older treated in an open-label extension of a phase 3 trial. Methods: Eligible patients (>= 4 attacks for more than 2 consecutive months) were randomized to receive twice-weekly subcutaneous C1-INH with a dosage of 40 IU/kg or 60 IU/kg for 52 to 140 weeks. Safety end points and efficacy outcomes were evaluated for patients aged 65 years and above and younger than 65 years. Results: Of the 126 patients treated, 10 were 65 years and older (mean age [range], 68 [65-72 years]). A total of 8 of 10 patients had multiple comorbidities, and 6 of these 10 patients were taking more than 5 non-HAE-related drugs concomitantly. AEs occurring in more than 1 patient included injection site bruising (n = 2, related), injection site pain (n = 2, related), urinary tract infection (n = 2, unrelated), and diarrhea (n = 2, unrelated). No thromboembolic events or cases of anaphylaxis were reported. Two patients aged 65 years and older experienced unrelated serious AEs (dehydration and hypokalemia in 1 and pneumonia and an HAE attack leading to hospitalization in another). A total of 6 of 9 evaluable patients were responders, with a greater than or equal to 50% reduction in HAE attacks vs prestudy; 6 of 10 patients had less than 1 attack over 4 weeks and 3 were attack-free (median attack rate, 0.52 attacks per month). Conclusion: Subcutaneous C1-INH was well-tolerated and effective in the management of HAE in patients aged 65 years and older with multiple comorbid conditions and polypharmacy. (C) 2020 American College of Allergy, Asthma & Immunology.
引用
收藏
页码:334 / +
页数:8
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