A Retrospective Analysis of Long-Term Prophylaxis with Berotralstat in Patients with Hereditary Angioedema and Acquired C1-Inhibitor Deficiency-Real-World Data

被引:11
作者
Johnson, Felix [1 ]
Stenzl, Anna [1 ]
Hofauer, Benedikt [1 ]
Heppt, Helen [1 ]
Ebert, Eva-Vanessa [2 ]
Wollenberg, Barbara [2 ]
Lochbaum, Robin [3 ]
Hahn, Janina [3 ]
Greve, Jens [3 ]
Trainotti, Susanne [2 ]
机构
[1] Med Univ Innsbruck, Univ Hosp Otorhinolaryngol, Head & Neck Surg, Anich str 35, A-6020 Innsbruck, Austria
[2] TUM Sch Med & Hlth, Klin Rechts Isar, Dept Otorhinolaryngol Head & Neck Surg, Dept Clin Med, Munich, Germany
[3] Ulm Univ, Med Ctr, Dept Otorhinolaryngol Head & Neck Surg, Ulm, Germany
关键词
Acquired angioedema; Hereditary angioedema; HAE; C1-INH-deficiency; AAE-C1-INH; Berotralstat; Bradykinin; Prophylaxis; Long-term prophylaxis; LTP; QUALITY-OF-LIFE; ICATIBANT; VALIDATION; INHIBITOR; DIAGNOSIS;
D O I
10.1007/s12016-023-08972-2
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Hereditary angioedema (HAE) and acquired C1-inhibitor deficiency (AAE-C1-INH) are orphan diseases. Berotralstat is a recently licensed long-term prophylaxis (LTP) and the first oral therapy for HAE patients. No approved therapies exist for AAE-C1-INH patients. This study is the first to report real-world clinical data of patients with AAE-C1-INH and HAE who received Berotralstat. All patients treated with Berotralstat were included in this retrospective, bi-centric study. Data was collected from patients' attack calendars and the angioedema quality of life (AE-QoL) and angioedema control test (AECT) questionnaires before treatment, and at 3, 6, and 12 months after treatment and was then analyzed. Twelve patients were included, 3 patients with AAE-C1-INH, 7 patients with HAE type I, and 2 patients with HAE-nC1-INH. One patient (HAE I) quit treatment. Berotralstat was associated with fewer attacks in all groups. After 6 months of treatment, a median decrease of attacks per month was noted for HAE type I patients (3.3 to 1.5) and AAE-C1-INH patients (2.3 to 1.0). No aerodigestive attacks were noted for AAE-C1-INH patients. For HAE-nC1-INH patients, a mean decrease from 3.8 to 1.0 was noted (3 months). For HAE I patients, the total AE-QoL lowered a mean of 24.1 points after 6 months, for HAE-nC1-HAE patients 8.0 points, and for AAE-C1-INH patients 13.7 points. AECT scores increased for HAE I patients (mean: 7.1), HAE-nC1-INH patients (9.0), and AAE-C1-INH patients (4.2) after 6 months. Patients with HAE, HAE-nC1-INH, and AAE-C1-INH treated with Berotralstat showed reduced angioedema attacks and improved AE-QoL and AECT scores.
引用
收藏
页码:354 / 364
页数:11
相关论文
共 31 条
[1]  
Afshan T, 2021, J ALLERGY CLIN IMMUN, V147, pAB20
[2]   Berotralstat for the prophylaxis of hereditary angioedema-Real-world evidence data from the United Kingdom [J].
Ahuja, Manisha ;
Dorr, Anthony ;
Bode, Eniola ;
Boulton, Anne P. R. ;
Buckland, Matthew ;
Chee, Samuel ;
Dalley, Claire ;
Denman, Sarah ;
Ekbote, Anjali ;
Elkhalifa, Shuayb ;
El-Shanawany, Tariq ;
Eren, Efrem ;
Herwadkar, Archana ;
Garcez, Tomaz ;
Ghanta, Harichandana ;
Grammatikos, Alexandros ;
Grigoriadou, Sofia ;
Jain, Rashmi ;
Lorenzo, Lorena ;
Manson, Ania ;
Moon, Emily ;
Murng, Sai ;
Murphy, Aveen ;
Mutlu, Leman ;
Peters, Nicholas ;
Sooriyakumar, Kavitha ;
Stroud, Catherine ;
Townsend, Katie ;
Yellon, Robert L. ;
Yong, Patrick ;
Kiani-Alikhan, Sorena .
ALLERGY, 2023, 78 (05) :1380-1383
[3]  
Anderson J, 2023, J ALLERGY CLIN IMMUN, V151, pAB135
[4]   Epidemiology of Bradykinin-mediated angioedema: a systematic investigation of epidemiological studies [J].
Aygoeren-Puersuen, Emel ;
Magerl, Markus ;
Maetzel, Andreas ;
Maurer, Marcus .
ORPHANET JOURNAL OF RARE DISEASES, 2018, 13
[5]   Angioedema Due to Acquired Deficiency of C1-Inhibitor: A Cohort Study in Spain and a Comparison With Other Series [J].
Baeza, Maria L. ;
Gonzalez-Quevedo, Teresa ;
Caballero, Teresa ;
Guilarte, Mar ;
Lleonart, Ramon ;
Varela, Susana ;
Castro, Monica ;
Diaz, Carmen ;
Escudero, Elena ;
Garcia, Marimar G. ;
Laffond, Elena ;
Munoz-Bellido, Francisco J. ;
Nunez, Ramon ;
Prior, Nieves ;
Sala-Cunill, Anna ;
de San Pedro, Blanca Saenz ;
Prieto-Garcia, Alicia .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2022, 10 (04) :1020-1028
[6]   Treatment for hereditary angioedema with normal C1-INH and specific mutations in the F12 gene (HAE-FXII) [J].
Bork, K. ;
Wulff, K. ;
Witzke, G. ;
Hardt, J. .
ALLERGY, 2017, 72 (02) :320-324
[7]   Angioedema due to acquired C1-inhibitor deficiency: spectrum and treatment with C1-inhibitor concentrate [J].
Bork, Konrad ;
Staubach-Renz, Petra ;
Hardt, Jochen .
ORPHANET JOURNAL OF RARE DISEASES, 2019, 14 (1)
[8]   BRADYKININ RECEPTOR 2 ANTAGONIST (ICATIBANT) FOR HEREDITARY ANGIOEDEMA TYPE III ATTACKS [J].
Bouillet, Laurence ;
Boccon-Gibod, Isabelle ;
Ponard, Denise ;
Drouet, Christian ;
Cesbron, Jean Yves ;
Dumestre-Perard, Chantal ;
Monnier, Nicole ;
Lunardi, Joel ;
Massot, Christian ;
Gompel, Anne .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2009, 103 (05) :448-448
[9]   Impaired control of the contact system in hereditary angioedema with normal C1-inhibitor [J].
Bova, Maria ;
Suffritti, Chiara ;
Bafunno, Valeria ;
Loffredo, Stefania ;
Cordisco, Giorgia ;
Del Giacco, Stefano ;
De Pasquale, Tiziana Maria Angela ;
Firinu, Davide ;
Margaglione, Maurizio ;
Montinaro, Vincenzo ;
Petraroli, Angelica ;
Radice, Anna ;
Brussino, Luisa ;
Zanichelli, Andrea ;
Zoli, Alessandra ;
Cicardi, Marco .
ALLERGY, 2020, 75 (06) :1394-1403
[10]   Acquired C1-Inhibitor Deficiency: 7 Patients Treated with Rituximab [J].
Branellec, Albanne ;
Bouillet, Laurence ;
Javaud, Nicolas ;
Mekinian, Arsene ;
Boccon-Gibod, Isabelle ;
Blanchard-Delaunay, Claire ;
Oksenhendler, Eric ;
Ollivier, Yann ;
Dunogue, Bertrand ;
Amarger, Stephanie ;
Ponard, Denise ;
Drouet, Christian ;
Mouthon, Luc ;
Thomas, Michel ;
Fain, Olivier .
JOURNAL OF CLINICAL IMMUNOLOGY, 2012, 32 (05) :936-941