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Octreotide treatment of acromegaly. A randomized, multicenter study.
- Source :
- Annals of Internal Medicine; 11/1/92, Vol. 117 Issue 9, p711-718, 8p
- Publication Year :
- 1992
-
Abstract
- <bold>Objective: </bold>To determine the effects of the somatostatin analog, octreotide acetate, in patients with acromegaly.<bold>Design: </bold>Double-blind, randomized trial.<bold>Setting: </bold>Fourteen university-affiliated medical centers.<bold>Patients: </bold>One hundred fifteen acromegalic patients, 70% of whom had persistent disease after pituitary surgery or radiotherapy.<bold>Intervention: </bold>Subcutaneous octreotide, 100 micrograms, or placebo every 8 hours for 4 weeks. Four weeks after the end of treatment, patients were randomized to receive 100 or 250 micrograms octreotide subcutaneously every 8 hours for 6 months.<bold>Results: </bold>After 2 weeks of treatment, a single 100-micrograms injection reduced mean serum growth hormone (GH) to 30% of the pretreatment concentration within 2 hours. The integrated mean GH level was reduced over 8 hours from 39 +/- 11 micrograms/L to 9 +/- 2 micrograms/L (P less than 0.001). Mean plasma insulin-like growth factor-1 (IGF-1) was reduced from 5100 +/- 400 U/L to 2400 +/- 400 U/L (P less than 0.001). After 6 months, the mean GH was reduced from 39 +/- 13 to 15 +/- 4 micrograms/L by 300 micrograms of octreotide and from 29 +/- 5 micrograms/L to 9 +/- 2 micrograms/L by 750 micrograms of octreotide daily. The mean IGF-1 concentration was suppressed to 2100 +/- 300 and 2500 +/- 400 U/L after 300 and 750 micrograms octreotide, respectively. Integrated mean GH levels were reduced to < 5 micrograms/L in 53% (95% CI, 39% to 67%) and 49% (CI, 35% to 63%), and IGF-1 levels were normal in 68% (CI, 54% to 82%) and 55% (CI, 40% to 70%) of patients receiving low- and high-dose octreotide, respectively. A substantial decrease in headache, amount of perspiration, joint pain, and finger circumference occurred in two thirds of the patients. The pituitary size was reduced in 19% (CI, 5% to 33%) and 37% (CI, 22% to 52%) of patients receiving 6 months of low- and high-dose octreotide, respectively. Ten percent and 13% of patients in each treatment group developed transient diarrhea; 10% and 14%, biliary sludge; and 6% and 18%, cholelithiasis, respectively.<bold>Conclusion: </bold>Octreotide effectively decreased GH and IGF-1 concentrations in 53% and 68% of patients, respectively. The higher dose resulted in increased frequency of tumor shrinkage but added no biochemical or clinical benefit. [ABSTRACT FROM AUTHOR]
- Subjects :
- ACROMEGALY
ADENOMA
AMINO acids
CLINICAL trials
COMPARATIVE studies
DOCUMENTATION
LONGITUDINAL method
RESEARCH methodology
MEDICAL cooperation
OCTREOTIDE acetate
PITUITARY tumors
RESEARCH
SOMATOMEDIN
EVALUATION research
HUMAN growth hormone
RANDOMIZED controlled trials
BLIND experiment
DISEASE complications
Subjects
Details
- Language :
- English
- ISSN :
- 00034819
- Volume :
- 117
- Issue :
- 9
- Database :
- Complementary Index
- Journal :
- Annals of Internal Medicine
- Publication Type :
- Academic Journal
- Accession number :
- 137743827
- Full Text :
- https://doi.org/10.7326/0003-4819-117-9-711