Primary medical therapy for acromegaly: An open, prospective, multicenter study of the effects of subcutaneous and intramuscular slow-release octreotide on growth hormone, insulin-like growth factor-I, and tumor size

被引:205
作者
Bevan, JS [1 ]
Atkin, SL
Atkinson, AB
Bouloux, PM
Hanna, F
Harris, PE
James, RA
McConnell, M
Roberts, GA
Scanlon, MF
Stewart, PM
Teasdale, E
Turner, HE
Wass, JAH
Wardlaw, JM
机构
[1] Aberdeen Royal Infirm, Dept Endocrinol, Aberdeen AB25 2ZN, Scotland
[2] Hull Royal Infirm, Dept Endocrinol, Kingston Upon Hull HU3 3KZ, N Humberside, England
[3] Royal Victoria Hosp, Dept Endocrinol, Belfast BT12 6BA, Antrim, North Ireland
[4] Royal Free Hosp, Dept Endocrinol, London NW3 2QQ, England
[5] Univ Wales Hosp, Dept Endocrinol, Cardiff CF4 4XN, S Glam, Wales
[6] Kings Coll Hosp, Dept Endocrinol, London SE5 9RS, England
[7] Royal Victoria Infirm, Dept Endocrinol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[8] Queen Elizabeth Hosp, Dept Endocrinol, Birmingham B15 2TH, W Midlands, England
[9] Radcliffe Infirm, Dept Endocrinol, Oxford OX2 6HE, England
[10] So Gen Hosp, Dept Neuroradiol, Glasgow G51 4TF, Lanark, Scotland
[11] Western Gen Hosp, Dept Neuroradiol, Edinburgh EH4 2XU, Midlothian, Scotland
关键词
D O I
10.1210/jc.2001-012012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Conventional surgery and radiotherapy for acromegaly have limitations. There are few data on the use of the somatostatin analog octreotide (Oct) as primary medical therapy. An open prospective study of 27 patients with newly diagnosed acromegaly was conducted in nine endocrine centers in the United Kingdom. Twenty patients had macroadenomas, and 7 had microadenomas. For the first 24 wk (phase 1), patients received sc Oct in an initial dose of 100 mug, 3 times daily, increased to 200 mug three times daily after 4 wk in the 13 patients whose mean serum GH remained greater than 5 mU/liter (2 mug/liter). Five-point GH profiles were performed at 0, 4,12, and 24 wk, and high resolution pituitary imaging using a standard protocol was performed at 0, 12, and 24 wk (magnetic resonance imaging in 25 patients and computed tomography in 2). Tumor dimensions and volumes were calculated by a central, reporting neuroradiologist, and the results were audited by a second, independent neuroradiologist. After 24 wk, 15 patients proceeded to phase 2 of the study with a direct switch to monthly injections of the depot formulation of Oct, Sandostatin long-acting release (Oct-LAR). Further GH profiles were performed at 36 and 48 wk, and pituitary imaging was performed at 48 wk. The median pretreatment serum GH concentration was 30.7 mU/liter (range, 6.7-141.4). During se Oct, serum GH fell to less than 5 mU/liter in 9 patients (38%), and IGF-I fell to normal in 8 patients (33%). All 27 tumors shrank during sc Oct; for microadenomas the median tumor volume reduction was 49% (range, 12-73), and for macroadenomas it was 43% (range, 6-92). After 24 wk of Oct-LAR (end of phase 2), the GH level was less than 5 mU/Iiter in 11 of 14 patients (79%), and IGF-I was normal in 8 of 15 patients (53%). In the 15 patients given Oct-LAR (10 macroadenomas), wk 48 scans showed a further overall median tumor volume reduction of 24%. At the end of the study 79% of patients had mean serum GH levels below 5 mU/liter, 53% had normal IGF-I levels, and 73% showed greater than 30% tumor shrinkage. Twenty-nine percent of patients achieved all 3 targets, but no patient with pretreatment GH levels above 50 mU/Iiter did so at any stage of the study. Primary medical therapy with Oct offers the prospect of normalization of GH/IGF-I levels together with substantial tumor shrinkage in a significant subset of acromegalic patients. This is most likely to occur in patients with pretreatment GH levels less than 50 mU/Iiter (20 mug/liter).
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页码:4554 / 4563
页数:10
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