Literature DB >> 12545148

Population pharmacodynamic analysis of octreotide in acromegalic patients.

Emmanuelle Comets1, France Mentré, Peter Grass, Ryosei Kawai, Peter Marbach, Jacky Vonderscher.   

Abstract

INTRODUCTION: Octreotide is an octapeptide analog of somatostatin used to normalize growth hormone levels in acromegaly. This article presents a population analysis of the relationship between octreotide and growth hormone concentrations in 94 patients with acromegaly, including 10 patients responding incompletely to subcutaneous treatment (poor responders).
METHODS: Growth hormone and octreotide concentrations were recorded hourly over 12-hour time periods during long-term subcutaneous treatment. Twelve-hour profiles were also collected on different days up to 2 months after intramuscular injection of the long-acting formulation. We modeled the inhibition of growth hormone secretion by octreotide with a direct maximum inhibition model. A joint analysis of both formulations was performed with NONMEM (GloboMax, LLC, Hanover, Md). During model building, we examined the relationships between parameters and demographic covariates or formulations with the use of likelihood ratio tests.
RESULTS: The baseline growth hormone level was higher in poor responders and was best described by a bimodal distribution. The maximum inhibition was common to both formulations and had a mean of 90%, with low interindividual variability. Sensitivity to octreotide (50% inhibitory concentration) was found to be slightly lower on average with intramuscular administration than with subcutaneous administration.
CONCLUSION: Given adequate doses of octreotide, in 72% of 94 patients, growth hormone would decrease to levels below 2.5 ng. mL(-1), considered to be a desirable target concentration in acromegaly. This study provides a way to identify poor responders during subcutaneous treatment, allowing an early clinical decision to be made to switch nonresponders to alternative therapies.

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Year:  2003        PMID: 12545148     DOI: 10.1067/mcp.2003.6

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  4 in total

1.  Approaches to handling pharmacodynamic baseline responses.

Authors:  Chantaratsamon Dansirikul; Hanna E Silber; Mats O Karlsson
Journal:  J Pharmacokinet Pharmacodyn       Date:  2008-04-30       Impact factor: 2.745

2.  Population pharmacokinetic/pharmacodynamic modelling of the analgesic effects of tramadol in pediatrics.

Authors:  María J Garrido; Walid Habre; Ferdinand Rombout; Iñaki F Trocóniz
Journal:  Pharm Res       Date:  2006-08-09       Impact factor: 4.200

3.  Effect of pasireotide on glucose- and growth hormone-related biomarkers in patients with inadequately controlled acromegaly.

Authors:  Herbert A Schmid; Thierry Brue; Annamaria Colao; Mônica R Gadelha; Ilan Shimon; Karen Kapur; Alberto M Pedroncelli; Maria Fleseriu
Journal:  Endocrine       Date:  2016-02-23       Impact factor: 3.633

4.  Quantification of the endogenous growth hormone and prolactin lowering effects of a somatostatin-dopamine chimera using population PK/PD modeling.

Authors:  Michiel J van Esdonk; Jacobus Burggraaf; Marion Dehez; Piet H van der Graaf; Jasper Stevens
Journal:  J Pharmacokinet Pharmacodyn       Date:  2020-04-04       Impact factor: 2.745

  4 in total

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