» Articles » PMID: 22574156

Meta-analysis on the Effects of Octreotide on Tumor Mass in Acromegaly

Overview
Journal PLoS One
Date 2012 May 11
PMID 22574156
Citations 68
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The long-acting somatostatin analogue octreotide is used either as an adjuvant or primary therapy to lower growth hormone (GH) levels in patients with acromegaly and may also induce pituitary tumor shrinkage.

Objective: We performed a meta-analysis to accurately assess the effect of octreotide on pituitary tumor shrinkage.

Data Sources: A computerized Medline and Embase search was undertaken to identify potentially eligible studies.

Study Eligibility Criteria: Eligibility criteria included treatment with octreotide, availability of numerical metrics on tumor shrinkage and clear definition of a clinically relevant reduction in tumor size. Primary endpoints included the proportion of patients with tumor shrinkage and mean percentage reduction in tumor volume.

Data Extraction And Analysis: The electronic search identified 2202 articles. Of these, 41 studies fulfilling the eligibility criteria were selected for data extraction and analysis. In total, 1685 patients were included, ranging from 6 to 189 patients per trial. For the analysis of the effect of octreotide on pituitary tumor shrinkage a random effect model was used to account for differences in both effect size and sampling error.

Results: Octreotide was shown to induce tumor shrinkage in 53.0% [95% CI: 45.0%-61.0%] of treated patients. In patients treated with the LAR formulation of octreotide, this increased to 66.0%, [95% CI: 57.0%-74.0%). In the nine studies in which tumor shrinkage was quantified, the overall weighted mean percentage reduction in tumor size was 37.4% [95% CI: 22.4%-52.4%], rising to 50.6% [95% CI: 42.7%-58.4%] with octreotide LAR.

Limitations: Most trials examined were open-label and had no control group.

Conclusions: Octreotide LAR induces clinically relevant tumor shrinkage in more than half of patients with acromegaly.

Citing Articles

Predictors of biochemical and structural response to medical therapy in patients with active acromegaly following surgery: a real-world perspective.

Rafieemanesh M, Kachuee M, Mehrjardi A, Khajavi A, Ghorbani M, Mohajeri-Tehrani M BMC Endocr Disord. 2025; 25(1):30.

PMID: 39901117 PMC: 11789350. DOI: 10.1186/s12902-025-01856-w.


The paradoxical GH response at OGTT does not predict Pasireotide efficacy but matters for glucose metabolism.

Occhi G, Voltan G, Chiloiro S, Bianchi A, Maffei P, Dassie F J Endocrinol Invest. 2025; .

PMID: 39841390 DOI: 10.1007/s40618-025-02534-3.


Acromegaly: diagnostic challenges and individualized treatment.

Freda P Expert Rev Endocrinol Metab. 2025; 20(1):63-85.

PMID: 39757391 PMC: 11832332. DOI: 10.1080/17446651.2024.2448784.


Standards of care for medical management of acromegaly in pituitary tumor centers of excellence (PTCOE).

Giustina A, Uygur M, Frara S, Barkan A, Biermasz N, Chanson P Pituitary. 2024; 27(4):381-388.

PMID: 38833044 PMC: 11289172. DOI: 10.1007/s11102-024-01397-w.


Clinical Pharmacology of Oral Octreotide Capsules for the Treatment of Acromegaly.

Uygur M, Villanova M, Frara S, Giustina A touchREV Endocrinol. 2024; 20(1):37-42.

PMID: 38812667 PMC: 11132652. DOI: 10.17925/EE.2024.20.1.9.


References
1.
Plockinger U, Reichel M, Fett U, Saeger W, Quabbe H . Preoperative octreotide treatment of growth hormone-secreting and clinically nonfunctioning pituitary macroadenomas: effect on tumor volume and lack of correlation with immunohistochemistry and somatostatin receptor scintigraphy. J Clin Endocrinol Metab. 1994; 79(5):1416-23. DOI: 10.1210/jcem.79.5.7962337. View

2.
Mercado M, Borges F, Bouterfa H, Chang T, Chervin A, Farrall A . A prospective, multicentre study to investigate the efficacy, safety and tolerability of octreotide LAR (long-acting repeatable octreotide) in the primary therapy of patients with acromegaly. Clin Endocrinol (Oxf). 2007; 66(6):859-68. PMC: 1974838. DOI: 10.1111/j.1365-2265.2007.02825.x. View

3.
Freda P, Katznelson L, van der Lely A, Reyes C, Zhao S, Rabinowitz D . Long-acting somatostatin analog therapy of acromegaly: a meta-analysis. J Clin Endocrinol Metab. 2005; 90(8):4465-73. DOI: 10.1210/jc.2005-0260. View

4.
Plewe G, Beyer J, Krause U, Neufeld M, Del Pozo E . Long-acting and selective suppression of growth hormone secretion by somatostatin analogue SMS 201-995 in acromegaly. Lancet. 1984; 2(8406):782-4. DOI: 10.1016/s0140-6736(84)90706-2. View

5.
Flogstad A, Halse J, Bakke S, Lancranjan I, Marbach P, Bruns C . Sandostatin LAR in acromegalic patients: long-term treatment. J Clin Endocrinol Metab. 1997; 82(1):23-8. DOI: 10.1210/jcem.82.1.3572. View