The role of growth hormone-receptor antagonism in relation to acromegaly

John Ayuk, Michael Sheppard

Research output: Contribution to journalReview article

4 Citations (Scopus)


Acromegaly is a rare but disabling condition associated with reduced life expectancy. It is caused almost invariably by a growth hormone-secreting pituitary adenoma. Transsphenoidal surgery and/or radiotherapy are still considered to be the treatment of choice, but despite recent advances in both these forms of treatment, the overall surgical cure rate remains similar to 60%, and radiotherapy is characterised by delayed effect and a high incidence of hypopituitarism. Medical therapy in the form of dopamine agonists and somatostatin analogues has traditionally been used as an adjunct to surgery and/or radiotherapy, but is increasingly being used as first line therapy in the treatment of acromegaly. Recently, a third form of medical therapy, the growth hormone receptor antagonist, pegvisomant, has been licensed for use in acromegaly. This article examines the design, properties, clinical efficacy and safety of pegvisomant.
Original languageEnglish
Pages (from-to)2279-2285
Number of pages7
JournalExpert Opinion on Pharmacotherapy
Publication statusPublished - 1 Nov 2004


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