Pasireotide Responsiveness in Acromegaly Is Mainly Driven by Somatostatin Receptor Subtype 2 Expression

J Clin Endocrinol Metab. 2019 Mar 1;104(3):915-924. doi: 10.1210/jc.2018-01524.

Abstract

Background: The response to first-generation somatostatin receptor ligands (SRLs) treatment in acromegaly correlates with expression of somatostatin receptor subtype 2 (SSTR2). However, pasireotide shows the highest binding affinity for SSTR subtype 5 (SSTR5). It has been suggested that in acromegaly, SSTR5 expression is better at predicting the response to pasireotide long-acting release (PAS-LAR) treatment than SSTR2 expression.

Aim: To investigate in patients with active acromegaly whether response to SRL treatment correlates to PAS-LAR treatment and to what extent SSTR2 and SSTR5 expression are correlated to the response to PAS-LAR treatment.

Methods: We included 52 patients from a cohort that initially received SRL treatment, followed by SRL and pegvisomant combination treatment, and finally PAS-LAR treatment. The long-term response to PAS-LAR was evaluated using a PAS-LAR score. In 14 out of 52 patients, somatotroph adenoma tissue samples were available to evaluate SSTR2 and SSTR5 expression using a previously validated immunoreactivity score (IRS).

Results: The percentage IGF-I (times the upper limit of normal) reduction, which was observed after SRL treatment, correlated with PAS-LAR response score during follow-up (r = 0.40; P = 0.003; n = 52). After exclusion of SRL-pretreated patients, SSTR2 IRS was positively correlated to PAS-LAR score (r = 0.58; P = 0.039; n = 9), whereas SSTR5 IRS showed no relation (r = 0.35; P = 0.36; n = 9).

Conclusions: In a cohort of patients partially responsive to SRLs, the IGF-I-lowering effects of PAS-LAR treatment correlated with the effect of SRL treatment and seemed to be mainly driven by SSTR2 expression instead of SSTR5.

MeSH terms

  • Acromegaly / blood
  • Acromegaly / drug therapy*
  • Acromegaly / etiology
  • Adult
  • Aged
  • Aged, 80 and over
  • Delayed-Action Preparations / pharmacology
  • Delayed-Action Preparations / therapeutic use
  • Female
  • Growth Hormone-Secreting Pituitary Adenoma / blood
  • Growth Hormone-Secreting Pituitary Adenoma / complications
  • Growth Hormone-Secreting Pituitary Adenoma / drug therapy*
  • Hormone Antagonists / pharmacology*
  • Hormone Antagonists / therapeutic use
  • Human Growth Hormone / analogs & derivatives
  • Human Growth Hormone / pharmacology
  • Human Growth Hormone / therapeutic use
  • Humans
  • Insulin-Like Growth Factor I / analysis
  • Male
  • Middle Aged
  • Pituitary Gland / drug effects
  • Pituitary Gland / metabolism
  • Pituitary Gland / pathology
  • Receptors, Somatostatin / metabolism*
  • Somatostatin / analogs & derivatives*
  • Somatostatin / pharmacology
  • Somatostatin / therapeutic use
  • Treatment Outcome

Substances

  • Delayed-Action Preparations
  • Hormone Antagonists
  • IGF1 protein, human
  • Receptors, Somatostatin
  • SSTR2 protein, human
  • Human Growth Hormone
  • Somatostatin
  • Insulin-Like Growth Factor I
  • somatostatin receptor 5
  • pasireotide
  • pegvisomant