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2011, Number 4

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Rev Endocrinol Nutr 2011; 19 (4)

Bromocriptine and cabergoline resistant prolactinoma. A case report

Ferreira-Hermosillo A, Ramos-Bustamante L, Ramírez-Rentería C, Mercado M, Mendoza-Zubieta V
Full text How to cite this article

Language: Spanish
References: 9
Page: 163-166
PDF size: 98.74 Kb.


Key words:

Prolactinomas, dopamine agonists, cabergoline.

ABSTRACT

Prolactinomas are the most common pituitary tumors. Dopamine agonists (DA) are the treatment of first choice. The goal of treatment is the restoration of the gonadal axis, and the prevention of neurological complications, particularly cranial nerve and chiasm compression. Resistance to AD is defined as inability to normalize PRL levels and the lack of tumor shrinkage by 50% after 4 months of treatment with cabergoline at doses 3 mg per week or more. The mechanisms involved in DA resistance are not well understood but some theories point towards the reduction in the transcription of the gene that encodes the dopamine receptor D2 (DRD2), as well as to post-receptor abnormalities. Cabergoline is the most effective DA, however 5 to 15% of prolactinomas may be resistant to this drug; tumors that do not respond to bromocriptine often respond to cabergoline. The presence of resistance to both DA is a great challenge. Resistant and invasive tumors may be candidates for surgical treatment, radiation therapy, somatostatine analoges or chemotherapy with temozolomide, though the effectiveness of this last has not been proved yet.


REFERENCES

  1. Ciccarelli A, Daly AF, Beckers A. The epidemiology of prolactinomas. Pituitary 2005; 8: 3-6.

  2. Klibanski A. Prolactinomas. N Engl J Med 2010; 362: 1219-1226.

  3. Mancini T, Casanueva FF, Giustina A. Hyperprolactinemia and prolactinomas. Endocrinol Metab Clin North Am 2008; 37: 67-99.

  4. Gillan MP, Molitch ME, Lombardi G, Colao A. Advances in the treatment of prolactinomas. Endocr Rev 2006; 27: 485-534.

  5. Molitch ME. Pharmacologic resistance in prolactinoma patients. Pituitary 2005; 8: 43-52.

  6. Molitch ME. The cabergoline-resistant prolactinoma patient: New challenges. J Clin Endocrinol Metab 2008; 93: 4643-4645.

  7. Passos VQ, Fortes MA, Gianella-Neto D, Bronstein MD. Genes differentially expressed in prolactinomas responsive and resistant to dopamine agonists. Neuroendocrinology 2009; 89: 163-170.

  8. Delgrange E, Daems T, Verhelst J, Abs R, Maiter D. Characterization of resistance to the prolactin-lowering effects of cabergoline in macroprolactinomas: A study in 122 patients. Eur J Endocrinol 2009; 160: 747-752.

  9. Ono M, Miki N, Kawamata T, Makino R, Amano K, Seki T et al. Prospective study of high-dose cabergoline treatment of prolactinomas in 150 patients. J Clin Endocrinol Metab 2008; 93: 4721-4727.




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Rev Endocrinol Nutr. 2011;19