Therapeutic options in the management of acromegaly: focus on lanreotide Autogel^®

Review

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Authors: Ferdinand Roelfsema, Nienke R Biermasz, Alberto M Pereira, Johannes A Romijn

Published Date September 2008 Volume 2008:2(3) Pages 463 - 479

DOI: http://dx.doi.org/10.2147/BTT.S3356

Ferdinand Roelfsema, Nienke R Biermasz, Alberto M Pereira, Johannes A Romijn

Department of Endocrinology and Metabolism, Leiden University Medical Center, Leiden, The Netherlands

Background: In acromegaly, expert surgery is curative in only about 60% of patients. Postoperative radiation therapy is associated with a high incidence of hypopituitarism and its effect on growth hormone (GH) production is slow, so that adjuvant medical treatment becomes of importance in the management of many patients.

Objective: To delineate the role of lanreotide in the treatment of acromegaly.

Methods: Search of Medline, Embase, and Web of Science databases for clinical studies of lanreotide in acromegaly.

Results: Treatment with lanreotide slow release and lanreotide Autogel^® normalized GH and insulin-like growth factor-I (IGF-I) concentrations in about 50% of patients. The efficacy of 120 mg lanreotide Autogel^® on GH and IGF-I levels was comparable with that of 20 mg octreotide LAR. There were no differences in improvement of cardiac function, decrease in pancreatic β-cell function, or occurrence of side effects, including cholelithiasis, between octreotide LAR and lanreotide Autogel^®. When postoperative treatment with somatostatin analogs does not result in normalization of serum IGF-I and GH levels after noncurative surgery, pegvisomant alone or in combination with somatostatin analogs can control these levels in a substantial number of patients.

Keywords: acromegaly, lanreotide, somatostatin analog, growth hormone, pegvisomant