Literature DB >> 10396369

Comparison of monthly intramuscular injections of Sandostatin LAR with multiple subcutaneous injections of octreotide in the treatment of acromegaly; effects on growth hormone and other markers of growth hormone secretion.

S J Hunter1, J A Shaw, K O Lee, P J Wood, A B Atkinson, J S Bevan.   

Abstract

OBJECTIVE: To compare the effects of monthly intra-muscular injections of a long acting preparation of octreotide, Sandostatin LAR, with multiple daily subcutaneous injections of octreotide and to study the interrelationships between mean 24 h growth hormone profile, serum total and free IGF-1 levels, 24 h urinary growth hormone levels and serum IGFBP-3.
DESIGN: Patients were assessed by 24 h GH profile off octreotide or any other GH modifying drug therapy; on subcutaneous octreotide (200-600 micrograms daily in divided doses for six weeks); and 28 days after the second of two injections of Sandostatin LAR (20 mg by intra-muscular injection) administered 28 days apart. Serum total and free IGF-1, serum IGFBP-3 and 24 h urinary GH were also measured on each occasion.
RESULTS: Sandostatin LAR was well tolerated. None of the patients reported any adverse effect and all completed the study uneventfully. Mean GH off treatment was 10.1 +/- 3.0 micrograms/l falling equally significantly (P < 0.05) during therapy with subcutaneous octreotide to 3.0 +/- 0.7 micrograms/l and Sandostatin LAR to 2.8 +/- 0.7 micrograms/l. Fasting 0900 h GH was significantly reduced (P < 0.05) on Sandostatin LAR (3.0 +/- 0.7 micrograms/l) compared with subcutaneous octreotide (5.1 +/- 1.2 micrograms/l). Mean total IGF-1 off treatment was 658.6 +/- 56.1 micrograms/l and was reduced to a comparable extent with subcutaneous octreotide and Sandostatin LAR (466.0 +/- 59.7 and 448.6 +/- 59.5 micrograms/l respectively; both P < 0.05). Free IGF-1 off treatment was 3.1 +/- 0.6 micrograms/l and was reduced equally by subcutaneous octreotide and Sandostatin LAR (1.2 +/- 0.2 and 1.2 +/- 0.2 micrograms/l; both P < 0.05). IGFBP-3 was reduced to a greater extent during Sandostatin LAR than during subcutaneous octreotide (4518.2 +/- 247.3 vs 5132.8 +/- 280.7 micrograms/l; P < 0.05). Twenty-four hour urinary GH excretion was reduced to a comparable extent with both therapies. Highly significant positive correlations were found between mean 24 h GH levels and free IGF-1 (r = 0.66, P < 0.0001) and 24 h urinary GH excretion (r = 0.94, P < 0.0001). The relationships between mean 24 h GH levels and total IGF-1 and IGFBP-3 although significant showed less powerful correlations.
CONCLUSIONS: These results suggest that Sandostatin LAR is well tolerated and as effective as subcutaneous octreotide. In addition, urinary growth hormone and serum free IGF-1 may prove valuable for outpatient follow-up of acromegalic patients, as both correlate well with mean 24 h serum growth hormone levels.

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Year:  1999        PMID: 10396369     DOI: 10.1046/j.1365-2265.1999.00668.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  8 in total

1.  PEGylation of octreotide: II. Effect of N-terminal mono-PEGylation on biological activity and pharmacokinetics.

Authors:  Dong Hee Na; Kang Choon Lee; Patrick P DeLuca
Journal:  Pharm Res       Date:  2005-05-17       Impact factor: 4.200

2.  Long-acting octreotide LAR compared with lanreotide SR in the treatment of acromegaly.

Authors:  P Kendall-Taylor; M Miller; J Gebbie; S Turner; M al-Maskari
Journal:  Pituitary       Date:  2000-10       Impact factor: 4.107

3.  Time course of GH and IGF-1 levels following withdrawal of long-acting octreotide in acromegaly.

Authors:  Y Lorcy; S Dejager; P Chanson
Journal:  Pituitary       Date:  2000-11       Impact factor: 4.107

4.  Changes in acromegaly treatment over four decades in Spain: analysis of the Spanish Acromegaly Registry (REA).

Authors:  Gemma Sesmilo; Sonia Gaztambide; Eva Venegas; Antonio Picó; Carlos Del Pozo; Concepción Blanco; Elena Torres; Cristina Álvarez-Escolà; Carmen Fajardo; Rogelio García; Rosa Cámara; Ignacio Bernabeu; Alfonso Soto; Carles Villabona; Alicia Serraclara; Irene Halperin; Victoria Alcázar; Elisabet Palomera; Susan M Webb
Journal:  Pituitary       Date:  2013-03       Impact factor: 4.107

5.  Identification of chemically modified peptide from poly(D,L-lactide-co-glycolide) microspheres under in vitro release conditions.

Authors:  Santos B Murty; Jack Goodman; B C Thanoo; Patrick P DeLuca
Journal:  AAPS PharmSciTech       Date:  2003-10-13       Impact factor: 3.246

6.  Effectiveness of long-acting octreotide in suppressing hormonogenesis and tumor growth in thyrotropin-secreting pituitary adenomas: report of two cases.

Authors:  L Gourgiotis; M C Skarulis; F Brucker-Davis; E H Oldfield; N J Sarlis
Journal:  Pituitary       Date:  2001-08       Impact factor: 4.107

Review 7.  Octreotide long-acting release (LAR): a review of its use in the management of acromegaly.

Authors:  Kate McKeage; Susan Cheer; Antona J Wagstaff
Journal:  Drugs       Date:  2003       Impact factor: 9.546

8.  Twenty-four-hour growth hormone profiling in the assessment of acromegaly.

Authors:  Robert D'Arcy; C Hamish Courtney; Una Graham; Steven Hunter; David R McCance; Karen Mullan
Journal:  Endocrinol Diabetes Metab       Date:  2017-12-27
  8 in total

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