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The real life experience goes on: update after 4 years on the first cohort treated with lanadelumab at our center.
Buttgereit, Thomas; Vera Ayala, Carolina; Aykanat, Seda; Weller, Karsten; Gutsche, Annika; Maurer, Marcus; Magerl, Markus.
Affiliation
  • Buttgereit T; Institute of Allergology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
  • Vera Ayala C; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin, Germany.
  • Aykanat S; Institute of Allergology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
  • Weller K; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin, Germany.
  • Gutsche A; Institute of Allergology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
  • Maurer M; Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, Immunology and Allergology, Berlin, Germany.
  • Magerl M; Institute of Allergology, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Front Immunol ; 15: 1405317, 2024.
Article in En | MEDLINE | ID: mdl-38799421
ABSTRACT

Introduction:

Lanadelumab is a first-line long-term prophylaxis (LTP) in hereditary angioedema (HAE). Real-life data on its long-term efficacy and safety are limited. It is unknown whether patients using lanadelumab need short-term prophylaxis (STP).

Objectives:

To provide 4-year follow-up data for our first 34 patients treating with lanadelumab.

Methods:

Patients were assessed for their current injection interval, attacks, treatment satisfaction, disease control (AECT), quality of life impairment (AE-QoL), events that can induce attacks, and the use of STP since the start of their treatment with lanadelumab.

Results:

Of 34 patients who started lanadelumab treatment, 32 were still using it after 4 years, with a median injection interval of 33 (range 14-90) days. HAE patients (n=28) reported longer intervals, i.e. 35 (14-90) days, than patients with angioedema due to acquired C1 inhibitor deficiency (n=4, 23 (14-31) days). With their current injection intervals, used for a mean duration of 29 ± 17 months, patients reported a yearly attack rate of 0.3 ± 0.1. More than 70% of patients were attack-free since starting their current injection interval. All patients reported well-controlled disease, i.e. ≥10 points in the AECT; 21 patients had complete control (16 points). AE-QoL scores improved further compared to our initial report, most prominently in the fears/shame domain (-6 points). Treatment satisfaction was very high. No angioedema occurred after 146 of 147 potentially attack-inducing medical procedures without STP.

Conclusions:

Our results demonstrate the long-term efficacy and safety of lanadelumab in real-life and question the need for STP in patients who use effective LTP.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Angioedemas, Hereditary / Antibodies, Monoclonal, Humanized Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Angioedemas, Hereditary / Antibodies, Monoclonal, Humanized Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: Germany