Eur J Endocrinol
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


DOI: 10.1530/eje.0.1500473
European Journal of Endocrinology, Vol 150, Issue 4, 473-480
Copyright © 2004 by European Society of Endocrinology
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ashwell, S.
Right arrow Articles by James, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ashwell, S.
Right arrow Articles by James, R.

Clinical Studies

The efficacy and safety of lanreotide Autogel in patients with acromegaly previously treated with octreotide LAR

SG Ashwell, JS Bevan, OM Edwards, MM Harris, C Holmes, MA Middleton, and RA James

School of Clinical Medical Sciences, University of Newcastle upon Tyne, UK. s.g.ashwell@ncl.ac.uk

OBJECTIVE: Lanreotide Autogel is a sustained-release aqueous gel formulation supplied in a prefilled syringe, with injection volume <0.5 ml. The aim of this study was to establish the efficacy and safety of Autogel in patients with acromegaly previously treated with octreotide LAR. DESIGN: A 28-week, open, multicentre study. PATIENTS: Twelve patients with acromegaly, treated with 20 mg octreotide LAR for >4 months, with serum GH levels <10.0 mU/l. METHODS: Autogel (90 mg) was given every 28 days during weeks 0-12. At week 16 the dose was titrated based on GH levels at weeks 8 and 12. If GH levels were <2.0, 2.0-5.0, or >5.0 mU/l, Autogel was reduced to 60 mg, maintained at 90 mg, or increased to 120 mg respectively, for the next three injections. GH and IGF-I levels were reassessed at weeks 24 and 28. RESULTS: Ten patients completed the study. Five remained on 90 mg Autogel throughout the study; in two patients the dose was reduced to 60 mg from week 16; in three patients it was increased to 120 mg. Mean GH levels were: baseline, 3.0+/-1.7 mU/l; week 12, 3.5+/-1.8 mU/l; week 28, 3.3+/-1.6 mU/l (NS). Mean IGF-I levels were: baseline, 212+/-70 microg/l; week 12, 185+/-91 microg/l; week 28: 154+/-61 microg/l (P=0.027). Six patients at baseline and eight at week 28 had normalised GH and IGF-I levels. Three patients reported adverse events: musculoskeletal pain (n=2) and injection-site symptoms (n=1). CONCLUSIONS: Lanreotide Autogel is effective and well tolerated in patients with acromegaly. This study in a small group of patients with well-controlled acromegaly suggests that the majority of patients switched from 20 mg LAR to 90 mg Autogel will have equivalent or better disease control.


This article has been cited by other articles:


Home page
J. Clin. Endocrinol. Metab.Home page
R. D. Murray and S. Melmed
A Critical Analysis of Clinically Available Somatostatin Analog Formulations for Therapy of Acromegaly
J. Clin. Endocrinol. Metab., August 1, 2008; 93(8): 2957 - 2968.
[Abstract] [Full Text] [PDF]


Home page
J. Clin. Endocrinol. Metab.Home page
A. Colao, J. Marek, M. I. Goth, P. Caron, J. M. Kuhn, F. M. Minuto, and N. J. Weissman
No Greater Incidence or Worsening of Cardiac Valve Regurgitation with Somatostatin Analog Treatment of Acromegaly
J. Clin. Endocrinol. Metab., June 1, 2008; 93(6): 2243 - 2248.
[Abstract] [Full Text] [PDF]


Home page
J Clin PharmacolHome page
B. Astruc, P. Marbach, H. Bouterfa, C. Denot, M. Safari, A. Vitaliti, and M. Sheppard
Long-Acting Octreotide and Prolonged-Release Lanreotide Formulations Have Different Pharmacokinetic Profiles
J. Clin. Pharmacol., July 1, 2005; 45(7): 836 - 844.
[Abstract] [Full Text] [PDF]


Home page
Eur J EndocrinolHome page
J. Wass
Debulking of pituitary adenomas improves hormonal control of acromegaly by somatostatin analogues
Eur. J. Endocrinol., May 1, 2005; 152(5): 693 - 694.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 European Society of Endocrinology.