Treatment of Resistant Acromegaly with a Long-Acting Somatostatin Analogue (SMS 201-995)
- LUClNDA B. BARNARD, M.D.;
- GRANTHAM WILLIAM G., M.D., Ph.D.;
- PRESTON LAMBERTON, M.D.;
- THOMAS M. O'DORISIO, M.D.; and
- IVOR M. D. JACKSON, M.R.C.P.
Abstract
Six patients with resistant acromegaly were given a longacting somatostatin analogue (SMS 201-995) for 5 to 12 months. The clinical response was dramatic; relief of headache occurred within minutes of the injection. The mean 24-hour growth hormone levels fell acutely after the administration of 50 or 100 µg every 12 hours, especially in four patients with small tumors (p < 0.001). Dosages of up to 1500 µg/d were necessary to produce maximum lowering of growth hormone secretion in some patients. On long-term treatment, plasma somatomedin-C levels fell in all patients and became normal in four. Plasma immunoreactive levels of SMS 201-995 related inversely to growth hormone concentration: A reproducible threshold for growth hormone inhibition in five of the patients, ranging from 70 to 1200 pg/mL, was maintained for 6 to 8 hours after the injections. This somatostatin analogue is effective in the treatment of acromegaly, has no major side effects, and causes only transient changes in carbohydrate metabolism.
Article and Author Information
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▸From the Division of Endocrinology, Brown University, Rhode Island Hospital; Providence, Rhode Island; and the Division of Endocrinology and Metabolism, The Ohio State University; Columbus, Ohio.
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Grant support: in part by National Institutes of Health Grants AM34540 (Dr. Jackson) and RR-34 (Ohio State University Hospitals).
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▸Requests for reprints should be addressed to Dr. Ivor M. D. Jackson, Division of Endocrinology, Brown University, Rhode Island Hospital, 593 Eddy Street; Providence, RI 02902.
- © 1986 American College of Physicians
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