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Effects of a chronic treatment with octreotide in patients with functionless pituitary adenomas

B Merola1, A Colao, D Ferone

  • 1Department of Medical-Surgical Endocrinology, University Federico II, School of Medicine, Naples, Italy.

Hormone Research
|January 1, 1993
PubMed

Insights

Octreotide treatment significantly lowered growth hormone (GH) and insulin-like growth factor-I (IGF-I) in patients with functionless pituitary adenomas. It also impacted glucose metabolism and reduced alpha-subunit levels in some patients.

Area of Science:

  • Endocrinology
  • Oncology
  • Pharmacology

Background:

  • Functionless pituitary adenomas lack specific hormone hypersecretion but can cause mass effects.
  • Octreotide, a somatostatin analog, is used in treating various endocrine disorders.

Purpose of the Study:

  • To evaluate the effects of chronic octreotide treatment on functionless pituitary adenomas.
  • To assess hormonal changes, tumor markers, and clinical outcomes in patients receiving octreotide.

Main Methods:

  • 19 patients with functionless pituitary adenomas received chronic octreotide treatment.
  • Hormonal levels (GH, IGF-I, thyroid, adrenal, gonadal function, alpha-subunit), glucose tolerance tests, and visual fields were monitored.
  • Tumor mass was assessed via CT scans.

Main Results:

  • Octreotide significantly decreased GH and IGF-I levels in all patients.
  • Glucose metabolism was altered, with increased and delayed glucose response and decreased, delayed insulin response.
  • Serum alpha-subunit (alpha-SU) levels decreased significantly in 60% of patients with elevated levels.
  • No significant change in tumor mass was observed, except for one patient with improved visual fields and decreased alpha-SU.

Conclusions:

  • Octreotide effectively reduces GH and IGF-I in functionless pituitary adenomas and may decrease alpha-SU levels.
  • The drug's efficacy may depend on somatostatin receptor presence on adenoma cells.
  • Pituitary scintigraphy with 111In-octreotide could identify suitable candidates for octreotide therapy.

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