Efficacy of lanreotide Autogel® administered every 4–8 weeks in patients with acromegaly previously responsive to lanreotide microparticles 30 mg: a phase III trial
Authors:
- T. LucasTLT. Lucas
- the Spanish–Portuguese Multicentre Autogel Study Group on AcromegalyTAthe Spanish–Portuguese Multicentre Autogel Study Group on Acromegaly
- 18 July 2006
- journal article
- research article
- Published by Wiley in Clinical Endocrinology
- Vol. 65 (3) , 320-326
Abstract
Summary: Objective and design Depot somatostatin analogues are well accepted as either adjuvant or primary therapy for acromegaly, and their long dosage intervals facilitate adherence to treatment. Our objective was to evaluate whether lanreotide Autogel® 120 mg, every 4–8 weeks, was as effective in controlling acromegaly as lanreotide microparticles 30 mg, every 1–2 weeks.Patients design and measurements Patients who had used lanreotide microparticles 30 mg, ≥ 2 months prestudy, and had responded to treatment were recruited to this open, prospective, multicentre phase III trial. Three to five injections of lanreotide Autogel® 120 mg were administered. Lanreotide Autogel® 120 mg was injected every 4, 6 or 8 weeks in patients previously receiving lanreotide microparticles every 7, 10 or 14 days, respectively. GH and insulin‐like growth factor (IGF)‐1 levels were assessed one dosing interval after the final injections.Results Ninety‐eight patients were enrolled and 93 completed. Steady‐state GH concentrations demonstrated similar efficacy between the formulations (upper 95% confidence interval of the quotient, 77·7%). Mean (SE) GH levels were lower with lanreotide Autogel® than with lanreotide microparticles (3·8 (0·5) vs 4·3 (0·5) ng/ml; P < 0·001). GH levels < 2·5 ng/ml were observed in 54% and 46% of patients; 40% and 35% having GH < 2·5 ng/ml and normalized IGF‐1 with lanreotide Autogel® and microparticles, respectively. Symptoms were controlled better with lanreotide Autogel® and treatment was well accepted.Conclusions Lanreotide Autogel® 120 mg every 4–8 weeks, is at least as effective and as well tolerated in acromegaly as lanreotide microparticles 30 mg injected every 7–14 days.Keywords
This publication has 39 references indexed in Scilit:
- One‐year follow‐up of patients with acromegaly treated with fixed or titrated doses of lanreotide Autogel®Clinical Endocrinology, 2004
- Efficacy of the New Long-Acting Formulation of Lanreotide (Lanreotide Autogel) in the Management of AcromegalyThe Journal of Clinical Endocrinology & Metabolism, 2002
- Two-Year Follow-Up of Acromegalic Patients Treated with Slow Release Lanreotide (30 mg)The Journal of Clinical Endocrinology & Metabolism, 2000
- Human Somatostatin Receptor Subtypes in Acromegaly: Distinct Patterns of Messenger Ribonucleic Acid Expression and Hormone Suppression Identify Different Tumoral PhenotypesThe Journal of Clinical Endocrinology & Metabolism, 2000
- Long-Term Mortality after Transsphenoidal Surgery and Adjunctive Therapy for AcromegalyThe Journal of Clinical Endocrinology & Metabolism, 1998
- Transsphenoidal Microsurgery for Growth Hormone-Secreting Pituitary Adenomas: Initial Outcome and Long-Term ResultsThe Journal of Clinical Endocrinology & Metabolism, 1998
- Mortality and Cancer Incidence in Acromegaly: A Retrospective Cohort StudyThe Journal of Clinical Endocrinology & Metabolism, 1998
- Sandostatin® LAR®: A promising therapeutic tool in the management of acromegalic patientsMetabolism, 1996
- Slow release lanreotide treatment in acromegalic patients previously normalized by octreotideThe Journal of Clinical Endocrinology & Metabolism, 1994
- Determinants of clinical outcome and survival in acromegalyClinical Endocrinology, 1994