2008, Número 6
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Rev Med Inst Mex Seguro Soc 2008; 46 (6)
Tratamiento de la acromegalia con octreotida LAR
Sosa E, Espinosade-los-Monteros AL, González B, Vargas G, Mier F, Mercado M
Idioma: Español
Referencias bibliográficas: 29
Paginas: 651-658
Archivo PDF: 126.39 Kb.
RESUMEN
Introducción: si bien altamente eficaz, el tratamiento de la acromegalia con análogos de somatostatina tiene las desventajas de ser costoso, no curativo y que debe administrarse indefinidamente. Describimos la experiencia de nuestro centro en el tratamiento de la acromegalia con una dosis fija de 20 mg de octreotida LAR cada cuatro semanas.
Material y métodos: 97 pacientes, 71 con macroadenoma, tratados con 20 mg de octreotida LAR intramuscular cada cuatro semanas, en 23 de ellos como tratamiento primario. Se midió GH e IGF-1 a las cuatro semanas después de la tercera inyección y a partir de ese momento las evaluaciones ocurrieron a intervalos de tres a seis meses. En 27 pacientes no seleccionados se realizó una evaluación seis semanas después de la inyección del análogo de somatostatina.
Resultados: se consiguió una concentración de GH ‹ 2.5 ng/mL en 71, 75 y 83 % de los pacientes al tercer, sexto y duodécimo mes de seguimiento, respectivamente, mientras que 34, 38 y 32 % consiguieron normalizar el IGF-1. Ambas metas se lograron en 30, 33 y 32% al tercer, sexto y duodécimo mes, respectivamente. La tasa de éxito bioquímico fue la misma tanto para los pacientes con tratamiento médico primario como para los tratados de manera secundaria. Una concentración de GH ‹ 10 ng/mL se asoció con mala respuesta al tratamiento.
Conclusiones: con la dosis fija de 20 mg de octreótido LAR cada 28 días es posible lograr una tasa de control bioquímico comparable a la de otras series publicadas.
REFERENCIAS (EN ESTE ARTÍCULO)
Melmed S, Jackson I, Klibanski A. Current treatment guidelines for acromegaly. J Clin Endocrinol Metab 1998;83:2646-2652.
Melmed S, Casanueva FF, Cavagnini F, Chanson P, Frohman L, Grossman A, et al. Guidelines for acromegaly management. J Clin Endocrinol Metab 2002;87:4054-4058.
Giustina A, Melmed S. Acromegaly consensus: the next steps. J Clin Endocrinol Metab 2003;88:1913-1914.
Serri O, Beauregard, Hardy J. Long-term biochemical status and disease-related morbidity in 53 postoperative patients with acromegaly. J Clin Endocrinol Metab 2004;89:658-661.
Holdaway IM, Rajasoorya RC, Gamble GD. Factors influencing mortality in acromegaly. J Clin Endocrinol Metab 2004;89:667-674.
Nomikos P, Buchfelder M, Fahlbusch R. The outcome of surgery in 668 patients with acromegaly using current criteria of biochemical cure. Eur J Endocrinol 2005;152:379-387.
Espinosa-de-los-Monteros AL, Sosa E, Cheng S, Ochoa R, Sandoval C, Guinto G, et al. Biochemical evaluation of disease activity after pituitary surgery in acromegaly: a critical analysis of patients who spontaneously change disease status. Clin Endocrinol 2006;64:245-249.
Melmed S, Casanueva F, Cavagnini F, Chanson P, Frohman LA, Gaillard R, et al. Consensus statement medical management of acromegaly. Eur J Endocrinol 2005;153:737-740.
Freda PU. Somatostatin analougs in acromegaly. J Clin Endocrinol Metab 2002;87:3013-3018.
Sheppard MC. Primary medical therapy for acromegaly. Clin Endocrinol 2003;58:387-399.
Vance ML, Laws ER. Role of medical therapy in the management of acromegaly. Neurosurgery 2005; 56:877-885.
Bevan JS, Atkin SL, Atkinson AB, Bouloux PM, Hanna F, et al. 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. J Clin Endocrinol Metab 2002;87:4554-4563.
Newmann CB, Melmed S, Snyder PJ, Young WF, Boyajy LD, Levy R, et al. Safety and efficacy of long-term octreotide therapy of acromegaly: results of a multicenter trial in 103 patients—a clinical research center study. J Clin Endocrinol Metab 1995; 80:2768-2775.
Colao A, Ferone D, Marzullo P, Cappabianca P, Cirillo S, Boerlin V, et al. Long-term effects of depot long-acting somatostatin analog octreotide on hormone levels and tumor mass in acromegaly. J Clin Endocrinol Metab 2001;86:2779-2786.
Cozzi R, Atanasio R, Montini M, Pagani G, Lasio G, Lodrini S, et al. Four-year treatment with octreotide-long-acting repeatable in 110 acromegalic patients: predictive value of short-term results? J Clin Endocrinol Metab 2003;88:3090-3098.
Caron P, Beckers A, Cullen DR, Goth MI, Gutt B, Laurberg P, et al. Efficacy of the new long-acting formulation of lanreotide (lanreotide autogel) in the management of acromegaly. J Clin Endocrinol Metab 2002;87:99-104.
Cozzi R, Montini M, Attanasio R, Albizzi M, Lasio G, Lodrini S, et al. Primary treatment of acromegaly with octreotide LAR: a long-term (up to 9 years) prospective study of its efficacy in the control of disease activity and tumor shrinkage. J Clin Endocrinol Metab 2006;91:1397-1403.
Jallad SR, Musolino NRC, Salgado LR, Bronstein MD. Treatment of acromegaly with octreotide LAR: extensive experience in a Brazilian institution. Clin Endocrinol 2005;63:168-175.
Bevan JS. Clinical review: the antitumoral effects of somatostatin analog therapy in acromegaly. J Clin Endocrinol Metab 2005;90:1856-1863.
Melmed S, Stertnber R, Cook D, Klibanski A, Chanson P, Bonert V, et al. A critical analysis of pituitary tumor shrinkage during primary medical therapy in acromegaly. J Clin Endocrinol Metab 2005;90:4405-4410.
Colao A, Pivonello R, Auriemma RS, Broiganti F, Galdiero M, Tortora F, et al. Predictors of tumor shrinkage after primary therapy with somatostatin analogues in acromegaly. J Clin Endocrinol Metab 2006;91(6):2112-2118.
Spada A, Arosio M, Bochicchio L, Bazzoni L, Vallar M, Basseti G, Faglia G. Clinical, biochemical and morphological correlates in patients bearing growth hormone-secreting pituitary tumors with and without constitutively active adenylyl cyclase. J Clin Endocrinol Metab 1990; 71:1421-1426.
Barlier A, Gunz G, Zamora AJ, Morange-Ramos I, Figarella-Branger D, et al. Prognostic and therapeutic consequences of GSα mutations in somatotroph adenomas. J Clin Endocrinolo Metab 1998; 83:1604-1610.
Mendoza V, Sosa E, Espinosa-de-Los-Monteros AL, Salcedo M, Guinto G, Cheng S, Sandoval C, Mercado M. GSP alpha mutations in Mexican patients with acromegaly: potential impact on long term prognosis. Growth Horm IGF Res 2005;15: 28-32.
Shimon I, Yan X, Taylor JE, Weiss MH, Culler MD, Melmed S. Somatostatin receptor (SSTR) subtypeselective analogues differentially suppress in vitro growth hormone and prolactin in human pituitary adenomas. Novel potential therapy for functional pituitary tumors. J Clin Invest 1997;100:2386-2392.
Jaquet P, Saveanu A, Grunz G, Fina F, Zamora AJ, Grino M, et al. Human somatostatin receptor subtypes in acromegaly: distinct patterns of messenger ribonucleic acid expression and hormone suppression identify different tumoral phenotypes. J Clin Endocrinol Metab 2000;85: 781-792.
Biermasz NR, Van den Oever NC, Frolich M, Arias AM, Smit JW, Romijin JA, Roelfsema F. Sandostatin LAR in acromegaly: a 6-week injection interval suppresses GH secretion as effectively as a 4-week interval. Clin Endocrinol 2003;5:288-295.
Turner HE, Thomton-Jones VA, Wass JA. Systematic dose-extension of octreotide LAR: the importance of individual tailoring of treatment in patients with acromegaly. Clin Endocrinol 2004; 61:224-231.
Drake WM, Rowles SV, Roberts ME, Fode FK, Besser GM, Monson JP, et al. Insulin sensitivity and glucose tolerance improve in patients with acromegaly converted from depot octreotide to pegvisomant. Eur J Endocrinol 2003;149:521-527.