Pegvisomant treatment in acromegaly in clinical practice: Final results of the French ACROSTUDY (312 patients).


Journal

Annales d'endocrinologie
ISSN: 2213-3941
Titre abrégé: Ann Endocrinol (Paris)
Pays: France
ID NLM: 0116744

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 16 12 2020
revised: 19 03 2021
accepted: 21 05 2021
pubmed: 14 7 2021
medline: 23 3 2022
entrez: 13 7 2021
Statut: ppublish

Résumé

We report the final analysis of the French ACROSTUDY, using data revised and enriched since the 2013 interim analysis. Our objective was to validate the use of pegvisomant (PEGV) in the treatment of acromegaly and to determine efficacy and safety. Patients with acromegaly treated with PEGV and followed up for at least 5 years were included. Eighty-eight investigators from 62 clinical centers in France included patients from April 2007 to April 2014. PEGV dose and administration frequency were determined by the physicians, based on their clinical evaluation and local habits. No additional examinations beyond those performed in normal follow-up were required. Minimum recommended follow-up included check-ups at treatment initiation, 6 months, 12 months and then annually. In total, 312 patients were enrolled. Mean age was 46.1±14.3 years at introduction of PEGV. Median PEGV treatment duration was 6.3 years and median follow-up was 5.6 years. Median dose at initiation was 10mg/day. The percentages of patients with IGF-1 ≤ ULN (upper limit of normal) were 10% (n=300) at baseline, 54% at 6 months (n=278), and 61.7% (n=253) at 2 years, then stabilizing at 64.4% (n=180) at 5 years. Mean PEGV dose was 17.4±11.7mg in patients with controlled disease versus 21.1±17.3mg in those without control at 5 years. At 5 years, 21.8% of patients (54/248) were receiving >30mg PEGV per day. In patients with at least one pituitary imaging procedure during the 5-year follow-up (n=292), the most recent image showed stable tumor volume in 212 subjects (72.6%), increased volume in 13 (4.5%), and decreased volume in 30 (10.3%). No PEGV treatments were permanently discontinued due to transaminase elevation. There were no cases of liver failure. The French ACROSTUDY showed normalization of IGF-1 levels in 64.4% of a real-life cohort of patients, mostly with uncontrolled disease despite multiple prior therapies. Long-term follow-up showed a sustained effectiveness and good long-term safety.

Identifiants

pubmed: 34256010
pii: S0003-4266(21)00078-0
doi: 10.1016/j.ando.2021.05.004
pii:
doi:

Substances chimiques

IGF1 protein, human 0
Human Growth Hormone 12629-01-5
Insulin-Like Growth Factor I 67763-96-6
pegvisomant N824AOU5XV

Types de publication

Journal Article Multicenter Study Observational Study Validation Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

582-589

Informations de copyright

Copyright © 2021 The Authors. Published by Elsevier Masson SAS.. All rights reserved.

Auteurs

Sara Barraud (S)

CRESTIC EA 3804, université de Reims Champagne Ardenne, UFR Sciences Exactes et Naturelles, Moulin de la Housse, BP 1039, 51687 Reims cedex 2, France; Service d'Endocrinologie-Diabète-Nutrition, CHU de Reims, hôpital Robert Debré, avenue du Général Koenig, 51092 Reims cedex, France. Electronic address: sbarraud@chu-reims.fr.

Philippe Caron (P)

Service d'endocrinologie et maladies métaboliques, pôle cardio-vasculaire et métabolique, hôpital Larrey, CHU de Toulouse, 24, chemin de Pouvourville, TSA 30030, 31059 Toulouse cedex 9, France. Electronic address: caron.p@chu-toulouse.fr.

Isabelle Raingeard (I)

Maladies endocriniennes, hôpital Lapeyronie, CHRU de Montpellier, 295, avenue du Doyen Gaston Giraud, 34295 Montpellier cedex 5, France. Electronic address: i-raingeard@chu-montpellier.fr.

Hervé Lefebvre (H)

CHU de Rouen, 1, rue de Germont, 76031 Rouen cedex, France. Electronic address: Herve.Lefebvre@chu-rouen.fr.

Gérald Raverot (G)

Hospices civils de Lyon, hôpital Louis-Pradel, 59, boulevard Pinel, 69677 Bron cedex, France. Electronic address: gerald.raverot@chu-lyon.fr.

Christine Cortet-Rudelli (C)

CHR Lille, hôpital Claude-Huriez, rue Michel Polonovski, 59037 Lille, France. Electronic address: christine.cortet@chru-lille.fr.

Rachel Desailloud (R)

CHU d'Amiens, hôpital Nord, place Victor Pauchet, 80054 Amiens cedex 1, France. Electronic address: desailloud.rachel@chu-amiens.fr.

Robin Henocque (R)

Pfizer France, 23-25, avenue du Docteur Lannelongue, 75668 Paris cedex 14, France. Electronic address: Robin.Henocque@pfizer.com.

Yves Brault (Y)

Pfizer France, 23-25, avenue du Docteur Lannelongue, 75668 Paris cedex 14, France. Electronic address: Yves.Brault@pfizer.com.

Thierry Brue (T)

Department of Endocrinology, Centre de référence des maladies rares de l'hypophyse HYPO, hôpital de la Conception, AP-HM, 13005 Marseille, France; INSERM, U1251, Marseille Medical Genetics (MMG), Institut Marseille Maladies Rares (MarMaRa), Aix-Marseille université, Marseille, France. Electronic address: Thierry.BRUE@ap-hm.fr.

Philippe Chanson (P)

Centre de référence des maladies rares de l'hypophyse HYPO, AP-HP, Hôpital Bicêtre, 94275 Le Kremlin-Bicêtre, France; Signalisation Hormonale, Physiopathologie Endocrinienne et Métabolique, Université Paris-Saclay, university Paris-Sud, Inserm, Le Kremlin-Bicêtre, France. Electronic address: philippe.chanson@aphp.fr.

Brigitte Delemer (B)

CRESTIC EA 3804, université de Reims Champagne Ardenne, UFR Sciences Exactes et Naturelles, Moulin de la Housse, BP 1039, 51687 Reims cedex 2, France; Service d'Endocrinologie-Diabète-Nutrition, CHU de Reims, hôpital Robert Debré, avenue du Général Koenig, 51092 Reims cedex, France. Electronic address: bdelemer@chu-reims.fr.

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Classifications MeSH