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

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 octr...

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Autores principales: Giustina, Andrea, Mazziotti, Gherardo, Torri, Valter, Spinello, Maurizio, Floriani, Irene, Melmed, Shlomo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344864/
https://www.ncbi.nlm.nih.gov/pubmed/22574156
http://dx.doi.org/10.1371/journal.pone.0036411
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author Giustina, Andrea
Mazziotti, Gherardo
Torri, Valter
Spinello, Maurizio
Floriani, Irene
Melmed, Shlomo
author_facet Giustina, Andrea
Mazziotti, Gherardo
Torri, Valter
Spinello, Maurizio
Floriani, Irene
Melmed, Shlomo
author_sort Giustina, Andrea
collection PubMed
description 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.
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spelling pubmed-33448642012-05-09 Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly Giustina, Andrea Mazziotti, Gherardo Torri, Valter Spinello, Maurizio Floriani, Irene Melmed, Shlomo PLoS One Research Article 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. Public Library of Science 2012-05-04 /pmc/articles/PMC3344864/ /pubmed/22574156 http://dx.doi.org/10.1371/journal.pone.0036411 Text en Giustina et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Giustina, Andrea
Mazziotti, Gherardo
Torri, Valter
Spinello, Maurizio
Floriani, Irene
Melmed, Shlomo
Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly
title Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly
title_full Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly
title_fullStr Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly
title_full_unstemmed Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly
title_short Meta-Analysis on the Effects of Octreotide on Tumor Mass in Acromegaly
title_sort meta-analysis on the effects of octreotide on tumor mass in acromegaly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344864/
https://www.ncbi.nlm.nih.gov/pubmed/22574156
http://dx.doi.org/10.1371/journal.pone.0036411
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