Efficacy and Safety of Pegvisomant in the Treatment of Acromegaly

Arch Med Res. 2023 Dec;54(8):102884. doi: 10.1016/j.arcmed.2023.102884. Epub 2023 Sep 1.

Abstract

Pegvisomant, the first and currently only clinically available growth hormone receptor antagonist, is an effective therapeutic option for the medical treatment of acromegaly, a rare disorder characterized by excessive growth hormone secretion. With now over 20 years of real world experience, its safety and efficacy is well-established. However, several aspects of its clinical use are still controversially discussed. The high cost of pegvisomant has limited its use in several countries, and recent studies have reported a lower efficacy than the initial clinical trials. A reported increase in tumor volume under therapy varies between studies and has been attributed to either actual growth or re-expansion after cessation of somatostatin receptor ligand therapy. Furthermore, different combinations of pegvisomant and other therapeutic agents aiming at reduction of acromegaly disease activity have been proposed to increase or retain effectiveness while lowering side effects and cost. This review aims to assess current clinical data on the safety and efficacy of pegvisomant while also addressing controversies surrounding its use.

Keywords: Acromegaly; Drug-Related Side Effects and Adverse Reactions; Growth-hormone Secreting Pituitary Adenoma; Hormone Antagonists; Human Growth Hormone; Receptors; Somatotropin.

Publication types

  • Review

MeSH terms

  • Acromegaly* / chemically induced
  • Acromegaly* / drug therapy
  • Acromegaly* / pathology
  • Hormone Antagonists / adverse effects
  • Human Growth Hormone* / adverse effects
  • Humans
  • Insulin-Like Growth Factor I
  • Receptors, Somatotropin / therapeutic use

Substances

  • pegvisomant
  • Receptors, Somatotropin
  • Human Growth Hormone
  • Hormone Antagonists
  • Insulin-Like Growth Factor I