Literature DB >> 21148630

Coadministration of lanreotide Autogel and pegvisomant normalizes IGF1 levels and is well tolerated in patients with acromegaly partially controlled by somatostatin analogs alone.

Aart-Jan van der Lely1, Ignacio Bernabeu, Jan Cap, Philippe Caron, Annamaria Colao, Josef Marek, Sebastian Neggers, Pascal Birman.   

Abstract

OBJECTIVE: To evaluate the efficacy and safety of coadministered lanreotide Autogel (LA; 120  mg/month) and pegvisomant (40-120  mg/week) in acromegaly.
DESIGN: This is a 28-week, multicenter, open-label, single-arm sequential study.
METHODS: Patients (n=92) biochemically uncontrolled, on somatostatin analogs (SSAs) or using pegvisomant monotherapy entered a 4-month run-in taking LA (120  mg/month). Patients uncontrolled after the run-in period (n=57) entered a 28-week coadministration period, receiving LA 120  mg/month plus pegvisomant (60  mg once weekly, adapted every 8 weeks based on IGF1 levels to 40-80  mg once weekly or 40 or 60  mg twice weekly).
RESULTS: In total, 33 (57.9%) patients had normalized IGF1 following coadministration (P<0.0001 versus 30% minimum clinically relevant); median pegvisomant dose in normalized patients was 60  mg/week. IGF1 normalized at any time during coadministration in 45 (78.9%) patients (P<0.0001) with median pegvisomant dose at 60  mg/week. Being nondiabetic (odds ratio (OR): 4.65) and older (OR, upper versus lower quartile: 3.40) showed increased likelihood of normalization. Symptom reduction was greatest for arthralgia (-0.6 ± 1.6) and soft tissue swelling (-0.6 ± 1.8). Five patients reported treatment-emergent adverse events causing treatment withdrawal: three serious (treatment related - thrombocytopenia, urticaria; not treatment related - abdominal pain/vomiting) and two nonserious (hepatotoxicity and cytolytic hepatitis, both elevating alanine aminotransferase to >5 × upper limit of normal with normalization after withdrawal).
CONCLUSIONS: In patients partially controlled by SSAs, LA (120  mg/month) plus pegvisomant normalized IGF1 in 57.9% of patients after 7 months, at a median effective pegvisomant dose of 60  mg/week, and 78.9% at any time. In these patients, results suggest a pegvisomant-sparing effect versus daily pegvisomant monotherapy.

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Year:  2010        PMID: 21148630     DOI: 10.1530/EJE-10-0867

Source DB:  PubMed          Journal:  Eur J Endocrinol        ISSN: 0804-4643            Impact factor:   6.664


  22 in total

Review 1.  Current perspectives on the impact of clinical disease and biochemical control on comorbidities and quality of life in acromegaly.

Authors:  Federico Gatto; Claudia Campana; Francesco Cocchiara; Giuliana Corica; Manuela Albertelli; Mara Boschetti; Gianluigi Zona; Diego Criminelli; Massimo Giusti; Diego Ferone
Journal:  Rev Endocr Metab Disord       Date:  2019-09       Impact factor: 6.514

2.  Partial response to first generation SSA guides the choice and predict the outcome of second line therapy in acromegaly.

Authors:  Sabrina Chiloiro; Denise Costa; Rosa Lauretta; Valeria Mercuri; Emilia Sbardella; Irene Samperi; Marialuisa Appetecchia; Antonio Bianchi; Antonella Giampietro; Patrizia Gargiulo; Andrea M Isidori; Maurizio Poggi; Alfredo Pontecorvi; Laura De Marinis
Journal:  Endocrine       Date:  2022-08-20       Impact factor: 3.925

Review 3.  The role of combination medical therapy in the treatment of acromegaly.

Authors:  Dawn Shao Ting Lim; Maria Fleseriu
Journal:  Pituitary       Date:  2017-02       Impact factor: 4.107

Review 4.  Management options for persistent postoperative acromegaly.

Authors:  Nestoras Mathioudakis; Roberto Salvatori
Journal:  Neurosurg Clin N Am       Date:  2012-08-09       Impact factor: 2.509

5.  Effects of long-term combined treatment with somatostatin analogues and pegvisomant on cardiac structure and performance in acromegaly.

Authors:  Renata S Auriemma; Ludovica F S Grasso; Mariano Galdiero; Maurizio Galderisi; Claudia Pivonello; Chiara Simeoli; Maria Cristina De Martino; Rosario Ferrigno; Mariarosaria Negri; Cristina de Angelis; Rosario Pivonello; Annamaria Colao
Journal:  Endocrine       Date:  2016-06-13       Impact factor: 3.633

Review 6.  Lanreotide autogel(®): a review of its use in the treatment of patients with acromegaly.

Authors:  Celeste B Burness; Sohita Dhillon; Susan J Keam
Journal:  Drugs       Date:  2014-09       Impact factor: 9.546

Review 7.  The Effect of the Exon-3-Deleted Growth Hormone Receptor on Pegvisomant-Treated Acromegaly: A Systematic Review and Meta-Analysis.

Authors:  Sanne E Franck; Linda Broer; Aart Jan van der Lely; Peter Kamenicky; Ignacio Bernabéu; Elena Malchiodi; Patric J D Delhanty; Fernando Rivadeneira; Sebastian J C M M Neggers
Journal:  Neuroendocrinology       Date:  2016-08-12       Impact factor: 4.914

8.  Safety of long-term treatment with Pegvisomant: analysis of Spanish patients included in global ACROSTUDY.

Authors:  I Bernabeu; A Pico; E Venegas; J Aller; C Alvarez-Escolá; J A García-Arnés; M Marazuela; P Jonsson; N Mir; M García Vargas
Journal:  Pituitary       Date:  2016-04       Impact factor: 4.107

9.  Long-term treatment of somatostatin analog-refractory growth hormone-secreting pituitary tumors with pegvisomant alone or combined with long-acting somatostatin analogs: a retrospective analysis of clinical practice and outcomes.

Authors:  Antonio Bianchi; Ferdinando Valentini; Raffaella Iuorio; Maurizio Poggi; Roberto Baldelli; Marina Passeri; Antonella Giampietro; Linda Tartaglione; Sabrina Chiloiro; Marialuisa Appetecchia; Patrizia Gargiulo; Andrea Fabbri; Vincenzo Toscano; Alfredo Pontecorvi; Laura De Marinis
Journal:  J Exp Clin Cancer Res       Date:  2013-06-21

Review 10.  Current therapies and mortality in acromegaly.

Authors:  S Găloiu; C Poiană
Journal:  J Med Life       Date:  2015 Oct-Dec
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