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Androgen transition and management of hereditary angioedema long-term prophylaxis in real life: a single-center case series.
Hoarau, Cyrille; Maleki, Alireza; Bouillet, Laurence; Boccon-Gibod, Isabelle.
Afiliación
  • Hoarau C; Transversal Allergology and Clinical immunology department, Tours University Hospital, 2 boulevard Tonnellé, Tours, 37000, France. hoarauc@univ-tours.fr.
  • Maleki A; CREAK Competence center of Tours, Tours University Hospital, Tours, 37000, France. hoarauc@univ-tours.fr.
  • Bouillet L; ISCHIEMIA, Inserm UMR1327, 10 boulevard Tonnellé, Tours, 37032, France. hoarauc@univ-tours.fr.
  • Boccon-Gibod I; Transversal Allergology and Clinical immunology department, Tours University Hospital, 2 boulevard Tonnellé, Tours, 37000, France.
Orphanet J Rare Dis ; 19(1): 257, 2024 Jul 09.
Article en En | MEDLINE | ID: mdl-38978077
ABSTRACT

BACKGROUND:

Hereditary angioedema (HAE) is a rare and potentially life-threatening disease that manifests clinically as recurrent episodes of swelling affecting multiple anatomical locations. Long-term prophylaxis (LTP) aims to control the disease by preventing HAE attacks. Previously, treatments such as attenuated androgens have been used for LTP, but they have an unfavorable adverse effect profile. Today, these limitations may be overcome by patients transitioning to newer, targeted therapies including oral berotralstat and subcutaneous lanadelumab. This case series reports the transition process between different prophylactic therapies in a family with HAE in a real-world setting.

RESULTS:

Four adult patient cases from the same family who underwent transitions in HAE prophylaxis are presented. Three were female and one male. Two patients who transitioned to berotralstat were initially prescribed attenuated androgens. Two patients were not taking LTP at the time of initiating targeted treatment but had previously been prescribed tranexamic acid. The length of transition varied between the patients, with the longest time taken to stabilize on new therapy being 26 months. All patients received regular follow-up in person or by telephone and all four required an adjustment from their initial treatment plan.

CONCLUSIONS:

Transitioning between LTP in HAE may help improve control of attacks, avoid unwanted adverse effects, or better cater to individual patient preferences. Newer targeted therapies have been shown to be effective and should be discussed with patients. Shared decision-making is a tool that can aid these discussions. The transition journey between LTP therapies in HAE may not be straightforward and is specific to each patient. Physicians should consider complicating factors such as patient anxieties around changing treatment, adverse effects, preferred routes of administration, and speed of transition. Following patients closely during the transition period helps identify any issues, including difficulties with treatment adherence, and may allow the transition plan to be adapted when necessary.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Angioedemas Hereditarios / Andrógenos Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Angioedemas Hereditarios / Andrógenos Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2024 Tipo del documento: Article País de afiliación: Francia Pais de publicación: Reino Unido