ACROSTART: A retrospective study of the time to achieve hormonal control with lanreotide Autogel treatment in Spanish patients with acromegaly

AbstractObjectivesThe ACROSTART study was intended to determine the time to achieve normalization of GH and IGF-I levels in responding patients with acromegaly administered different dosage regimens of lanreotide Autogel (Somatuline ® Autogel ®). MethodsFrom March 2013 to October 2013, clinical data...

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Published in:Endocrinología, diabetes y nutrición. Vol. 66; no. 5; pp. 320 - 329
Main Authors: Álvarez-Escolá, Cristina, Venegas-Moreno, Eva María, García-Arnés, Juan Antonio, Blanco-Carrera, Concepción, Marazuela-Azpiroz, Mónica, Gálvez-Moreno, María Ángeles, Menéndez-Torre, Edelmiro, Aller-Pardo, Javier, Salinas-Vert, Isabel, Resmini, Eugenia, Torres-Vela, Elena María, Gonzalo-Redondo, María Ángeles, Vílchez-Joya, Ricardo, de Miguel-Novoa, María Paz, Halperín-Rabinovich, Irene, Páramo-Fernández, Concepción, de la Cruz-Sugranyes, Guillermo, Houchard, Aude, Picó-Alfonso, Antonio Miguel
Format: Journal Article
Language:English
Published: Elsevier España, S.L.U 01-05-2019
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Abstract AbstractObjectivesThe ACROSTART study was intended to determine the time to achieve normalization of GH and IGF-I levels in responding patients with acromegaly administered different dosage regimens of lanreotide Autogel (Somatuline ® Autogel ®). MethodsFrom March 2013 to October 2013, clinical data from 57 patients from 17 Spanish hospitals with active acromegaly treated with lanreotide for ≥4 months who achieved hormonal control (GH levels <2.5 ng/ml and/or normalized IGF-I levels in ≥2 measurements) were analyzed. The primary objective was to determine the time from start of lanreotide treatment to hormonal normalization. ResultsMedian patient age was 64 years, 21 patients were male, 39 patients had undergone surgery, and 14 patients had received radiotherapy. Median hormonal values at start of lanreotide treatment were: GH, 2.6 ng/ml; IGF-I, 1.6 × ULN. The most common starting dose of lanreotide was 120 mg (29 patients). The main initial regimens were 60 mg/4 weeks ( n= 13), 90 mg/4 weeks ( n= 6), 120 mg/4 weeks ( n= 13), 120 mg/6 weeks ( n= 6), and 120 mg/8 weeks ( n= 9). An initial treatment regimen with a long interval (≥6 weeks) was administered in 25 patients. Mean duration of lanreotide treatment was 68 months (7–205). Median time to achieve hormonal control was 4.9 months. Injections were managed without healthcare assistance in 13 patients. Median number of visits to endocrinologists until hormonal control was achieved was 3. Fifty-one patients were “satisfied”/“very satisfied” with treatment and 49 patients did not miss any dose. ConclusionsReal-life treatment with lanreotide Autogel resulted in early hormonal control in responding patients, with high treatment adherence and satisfaction despite disparity in starting doses and dosing intervals.
AbstractList AbstractObjectivesThe ACROSTART study was intended to determine the time to achieve normalization of GH and IGF-I levels in responding patients with acromegaly administered different dosage regimens of lanreotide Autogel (Somatuline ® Autogel ®). MethodsFrom March 2013 to October 2013, clinical data from 57 patients from 17 Spanish hospitals with active acromegaly treated with lanreotide for ≥4 months who achieved hormonal control (GH levels <2.5 ng/ml and/or normalized IGF-I levels in ≥2 measurements) were analyzed. The primary objective was to determine the time from start of lanreotide treatment to hormonal normalization. ResultsMedian patient age was 64 years, 21 patients were male, 39 patients had undergone surgery, and 14 patients had received radiotherapy. Median hormonal values at start of lanreotide treatment were: GH, 2.6 ng/ml; IGF-I, 1.6 × ULN. The most common starting dose of lanreotide was 120 mg (29 patients). The main initial regimens were 60 mg/4 weeks ( n= 13), 90 mg/4 weeks ( n= 6), 120 mg/4 weeks ( n= 13), 120 mg/6 weeks ( n= 6), and 120 mg/8 weeks ( n= 9). An initial treatment regimen with a long interval (≥6 weeks) was administered in 25 patients. Mean duration of lanreotide treatment was 68 months (7–205). Median time to achieve hormonal control was 4.9 months. Injections were managed without healthcare assistance in 13 patients. Median number of visits to endocrinologists until hormonal control was achieved was 3. Fifty-one patients were “satisfied”/“very satisfied” with treatment and 49 patients did not miss any dose. ConclusionsReal-life treatment with lanreotide Autogel resulted in early hormonal control in responding patients, with high treatment adherence and satisfaction despite disparity in starting doses and dosing intervals.
The ACROSTART study was intended to determine the time to achieve normalization of GH and IGF-I levels in responding patients with acromegaly administered different dosage regimens of lanreotide Autogel (Somatuline® Autogel®). From March 2013 to October 2013, clinical data from 57 patients from 17 Spanish hospitals with active acromegaly treated with lanreotide for ≥4 months who achieved hormonal control (GH levels <2.5ng/ml and/or normalized IGF-I levels in ≥2 measurements) were analyzed. The primary objective was to determine the time from start of lanreotide treatment to hormonal normalization. Median patient age was 64 years, 21 patients were male, 39 patients had undergone surgery, and 14 patients had received radiotherapy. Median hormonal values at start of lanreotide treatment were: GH, 2.6ng/ml; IGF-I, 1.6×ULN. The most common starting dose of lanreotide was 120mg (29 patients). The main initial regimens were 60mg/4 weeks (n=13), 90mg/4 weeks (n=6), 120mg/4 weeks (n=13), 120mg/6 weeks (n=6), and 120mg/8 weeks (n=9). An initial treatment regimen with a long interval (≥6 weeks) was administered in 25 patients. Mean duration of lanreotide treatment was 68 months (7–205). Median time to achieve hormonal control was 4.9 months. Injections were managed without healthcare assistance in 13 patients. Median number of visits to endocrinologists until hormonal control was achieved was 3. Fifty-one patients were “satisfied”/“very satisfied” with treatment and 49 patients did not miss any dose. Real-life treatment with lanreotide Autogel resulted in early hormonal control in responding patients, with high treatment adherence and satisfaction despite disparity in starting doses and dosing intervals. El objetivo del estudio ACROSTART era determinar el período de tiempo para lograr la normalización hormonal (GH e IGF-I) en pacientes con acromegalia respondedores al tratamiento considerando los regímenes de lanreótida Autogel (Somatuline® Autogel®) utilizados en la práctica clínica. Desde marzo de 2013 hasta octubre de 2013, en 17 hospitales españoles se analizaron los datos clínicos de 57 pacientes con acromegalia activa tratados con lanreótida durante ≥4 meses que lograron control hormonal (niveles de GH <2,5ng/ml y/o IGF-I normalizado en ≥2 evaluaciones). El objetivo principal fue determinar el período de tiempo desde el inicio del tratamiento con lanreótida hasta la normalización hormonal. La mediana de edad de los pacientes fue 64 años, 21 pacientes eran hombres, 39 pacientes habían recibido cirugía, 14 pacientes habían recibido radioterapia. Los valores hormonales medianos al inicio del tratamiento con lanreótida fueron GH: 2,6ng/ml, IGF-I: 1,6×LSN. La dosis inicial más frecuente de lanreótida fue de 120mg (29 pacientes). Los principales regímenes iniciales fueron 60mg/4 semanas (n=13), 90mg/4 semanas (n=6), 120mg/4 semanas (n=13), 120mg/6 semanas (n=6), 120mg/8 semanas (n=9). Se administró un régimen de intervalo prolongado (≥6 semanas) en 25 pacientes. La duración media del tratamiento con lanreótida fue de 68 meses (7–205). El tiempo medio hasta lograr el control hormonal fue de 4,9 meses. Las inyecciones se manejaron sin asistencia médica en 13 pacientes. La mediana del número de visitas al endocrinólogo hasta el control hormonal fue 3. Cincuenta y un pacientes estaban “satisfechos”/“muy satisfechos” con el tratamiento y 49 pacientes no olvidaron ninguna dosis. El tratamiento en la vida real con lanreótida Autogel condujo a un control hormonal temprano en pacientes que respondieron, con una alta adherencia al tratamiento y satisfacción con el tratamiento, a pesar de la disparidad de las dosis iniciales y los intervalos de dosificación.
Author Álvarez-Escolá, Cristina
Resmini, Eugenia
Aller-Pardo, Javier
Picó-Alfonso, Antonio Miguel
García-Arnés, Juan Antonio
de Miguel-Novoa, María Paz
Salinas-Vert, Isabel
Páramo-Fernández, Concepción
Houchard, Aude
Torres-Vela, Elena María
Vílchez-Joya, Ricardo
Venegas-Moreno, Eva María
Blanco-Carrera, Concepción
de la Cruz-Sugranyes, Guillermo
Gonzalo-Redondo, María Ángeles
Marazuela-Azpiroz, Mónica
Menéndez-Torre, Edelmiro
Gálvez-Moreno, María Ángeles
Halperín-Rabinovich, Irene
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CitedBy_id crossref_primary_10_1007_s12020_020_02529_5
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DocumentTitleAlternate ACROSTART: Estudio retrospectivo del período de tiempo para lograr el control hormonal con lanreótida Autogel en pacientes con acromegalia en la práctica clínica española
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Issue 5
Keywords Factor de crecimiento de la insulina (IGF-I)
Lanreotide
Patrones de dosificación
Somatulina Autogel
Acromegaly
Hormona del crecimiento (GH)
Dosage regimens
Growth hormone (GH)
Insulin-like growth factor (IGF-I)
Lanreótida
Somatuline Autogel
Acromegalia
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Snippet AbstractObjectivesThe ACROSTART study was intended to determine the time to achieve normalization of GH and IGF-I levels in responding patients with acromegaly...
The ACROSTART study was intended to determine the time to achieve normalization of GH and IGF-I levels in responding patients with acromegaly administered...
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SubjectTerms Acromegalia
Acromegaly
Dosage regimens
Endocrinology and Metabolism
Factor de crecimiento de la insulina (IGF-I)
Growth hormone (GH)
Hormona del crecimiento (GH)
Insulin-like growth factor (IGF-I)
Lanreotide
Lanreótida
Patrones de dosificación
Somatulina Autogel
Somatuline Autogel
Title ACROSTART: A retrospective study of the time to achieve hormonal control with lanreotide Autogel treatment in Spanish patients with acromegaly
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https://dx.doi.org/10.1016/j.endien.2019.05.002
Volume 66
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