Effects of lanreotide Autogel primary therapy on symptoms and quality-of-life in acromegaly

To evaluate the effects of lanreotide Autogel on patient-reported outcomes and association with biochemical control, using PRIMARYS data. PRIMARYS was a 1-year, open-label study of lanreotide Autogel (Depot in USA) 120 mg every 4 weeks in 90 treatment-naïve patients with acromegaly. Symptoms were as...

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Detalles Bibliográficos
Autores: Caron, Philippe J., Bevan, John S., Petersenn, Stephan, Houchard, Aude|||0000-0001-6248-8986, Sert, Caroline, Webb, Susan|||0000-0001-7052-6436
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:185474
Acceso en línea:https://ddd.uab.cat/record/185474
https://dx.doi.org/urn:doi:10.1007/s11102-015-0693-y
Access Level:acceso abierto
Palabra clave:Acromegaly
Lanreotide Autogel
Quality of life
Symptoms
Descripción
Sumario:To evaluate the effects of lanreotide Autogel on patient-reported outcomes and association with biochemical control, using PRIMARYS data. PRIMARYS was a 1-year, open-label study of lanreotide Autogel (Depot in USA) 120 mg every 4 weeks in 90 treatment-naïve patients with acromegaly. Symptoms were assessed using Patient-assessed Acromegaly Symptom Questionnaire (PASQ) and health-related quality of life (HRQoL) using the AcroQoL questionnaire. Correlations between PASQ and AcroQoL scores, and between PASQ/AcroQoL and growth hormone (GH)/insulin-like growth factor-1 (IGF-1) levels were also evaluated (post hoc). Acromegaly symptoms and HRQoL significantly improved from week 12 to week 48, with modest correlations at week 48 between PASQ total score (R = -0.55, p < 0.0001) and AcroQoL global and physical scores (R = -0.67, p < 0.0001). Approximately 60 % of patients achieved a minimal important difference (MID; improvement.