Characterization of resistance to the prolactin-lowering effects of cabergoline in macroprolactinomas: a study in 122 patients.

CONTEXT Macroprolactinomas poorly responsive to dopamine-agonists are often more aggressive and are usually termed 'resistant' but this clinical concept has always been defined empirically. OBJECTIVE To define resistance to cabergoline (CAB) on the basis of a dose-response relationship established in a large series of macroprolactinoma patients and to assess the influence of gender and tumor invasiveness on the response to treatment. DESIGN Retrospective study. METHODS One hundred and twenty-two patients (72 women and 50 men) primarily treated with CAB for at least 1 year were included. Main outcome measures were serum prolactin (PRL) and tumor size. RESULTS Normalization of PRL was obtained in 115 out of the 122 patients (94%). The majority of patients (96/115, 83%) were controlled with a CAB dose < or =1.5 mg/week. Most of the other patients (19/26) had only a partial resistance, responding to a further increase of the CAB dose. Beyond the dose of 3.5 mg/week, there was no clear advantage in further increasing the dose instead of continuing the treatment at the same dose. Most tumors (98/119 assessable cases, 82%) showed a significant shrinkage during CAB treatment. It was more likely to occur in cases of PRL normalization. Both cavernous sinus invasion and male gender were significantly and independently associated with partial or complete resistance to treatment. CONCLUSIONS Most macroprolactinomas primarily treated with CAB are adequately controlled with doses < or =1.5 mg/week. About 20% of patients, mainly men and/or those with invasive tumors will require a higher dose of CAB. We suggest defining such patients as resistant to CAB.

[1]  Jeroen J. Bax,et al.  Cabergoline and cardiac valve disease in prolactinoma patients: additional studies during long-term treatment are required. , 2008, European journal of endocrinology.

[2]  W. Bremner,et al.  Advances in male contraception. , 2008, Endocrine reviews.

[3]  L. Cavallo,et al.  Predictors of remission of hyperprolactinaemia after long‐term withdrawal of cabergoline therapy , 2007, Clinical endocrinology.

[4]  J. Wass,et al.  Nonsurgical cerebrospinal fluid rhinorrhea in invasive macroprolactinoma: incidence, radiological, and clinicopathological features. , 2007, The Journal of clinical endocrinology and metabolism.

[5]  B. Roth Drugs and valvular heart disease. , 2007, The New England journal of medicine.

[6]  A. Antonini,et al.  Valvular heart disease and the use of dopamine agonists for Parkinson's disease. , 2007, The New England journal of medicine.

[7]  W. Haverkamp,et al.  Dopamine agonists and the risk of cardiac-valve regurgitation. , 2007, The New England journal of medicine.

[8]  J. Schlechte,et al.  Management of resistant prolactinomas , 2006, Nature Clinical Practice Endocrinology &Metabolism.

[9]  N. Karavitaki,et al.  Do the limits of serum prolactin in disconnection hyperprolactinaemia need re‐definition? A study of 226 patients with histologically verified non‐functioning pituitary macroadenoma , 2006, Clinical endocrinology.

[10]  A. Colao,et al.  Advances in the treatment of prolactinomas. , 2006, Endocrine reviews.

[11]  D. Maiter,et al.  Influence of parasellar extension of macroprolactinomas defined by magnetic resonance imaging on their responsiveness to dopamine agonist therapy , 2006, Clinical endocrinology.

[12]  P. Marcos-Alberca,et al.  Cabergoline-related severe restrictive mitral regurgitation. , 2005, The New England journal of medicine.

[13]  G. Sassolas,et al.  Clinical and histological correlations in prolactinomas, with special reference to bromocriptine resistance , 2005, Acta Neurochirurgica.

[14]  P. Cappabianca,et al.  Outcome of cabergoline treatment in men with prolactinoma: effects of a 24-month treatment on prolactin levels, tumor mass, recovery of pituitary function, and semen analysis. , 2004, The Journal of clinical endocrinology and metabolism.

[15]  P. Cappabianca,et al.  Resistance to cabergoline as compared with bromocriptine in hyperprolactinemia: prevalence, clinical definition, and therapeutic strategy. , 2001, The Journal of clinical endocrinology and metabolism.

[16]  J. Davies,et al.  Recovery of growth hormone secretion following cabergoline treatment of macroprolactinomas , 2000, Clinical endocrinology.

[17]  P. Cappabianca,et al.  Macroprolactinoma shrinkage during cabergoline treatment is greater in naive patients than in patients pretreated with other dopamine agonists: a prospective study in 110 patients. , 2000, The Journal of clinical endocrinology and metabolism.

[18]  G. Krassas,et al.  Cabergoline as a First-Line Treatment in Newly Diagnosed Macroprolactinomas , 2000, Pituitary.

[19]  L. Brunereau,et al.  Cavernous sinus invasion by pituitary adenoma: MR imaging. , 2000, Radiology.

[20]  C. Raftopoulos,et al.  Cabergoline in the treatment of hyperprolactinemia: a study in 455 patients. , 1999, The Journal of clinical endocrinology and metabolism.

[21]  F. Trimarchi,et al.  Cabergoline: A first-choice treatment in patients with previously untreated prolactin-secreting pituitary adenoma , 1999, Journal of endocrinological investigation.

[22]  J. Donckier,et al.  Sex-related difference in the growth of prolactinomas: a clinical and proliferation marker study. , 1997, The Journal of clinical endocrinology and metabolism.

[23]  C. Wilson,et al.  Transsphenoidal pituitary resection for preoperative diagnosis of prolactin-secreting pituitary adenoma in women: long term follow-up. , 1996, The Journal of clinical endocrinology and metabolism.

[24]  J. Webster,et al.  A comparison of cabergoline and bromocriptine in the treatment of hyperprolactinemic amenorrhea , 1994, The New England journal of medicine.

[25]  B. Sherman,et al.  The natural history of untreated hyperprolactinemia: a prospective analysis. , 1989, The Journal of clinical endocrinology and metabolism.

[26]  D. K. Hamilton,et al.  Surgical Outcomes in Hyporesponsive Prolactinomas: Analysis of patients with Resistance or Intolerance to Dopamine Agonists , 2005, Pituitary.

[27]  M. Molitch Pharmacologic Resistance in Prolactinoma Patients , 2005, Pituitary.

[28]  I. Morange,et al.  Prolactinomas and resistance to dopamine agonists. , 1992, Hormone research.