» Articles » PMID: 30542321

Prolactinomas Resistant to Treatment With Dopamine Agonists: Long-Term Follow-Up of Six Cases

Overview
Specialty Endocrinology
Date 2018 Dec 14
PMID 30542321
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Prolactinomas are preferentially treated with dopamine agonists. However, a few adenomas are resistant to this treatment. To evaluate the characteristics of patients with resistance to dopamine agonists in the long-term. A retrospective study of six cases was made. Patients who did not achieve normalized prolactin blood concentrations and a reduction of more than 50% of the tumor volume with the minimum dose of 3.5 mg per week of cabergoline for 3 months or the maximum supported dose of bromocriptine for 6 months were considered resistant to dopamine agonists. Patients were followed up at the Clinic of Neurology and Endocrinology or the University Hospital of Brasilia. Six patients were selected. Three patients were initially treated with bromocriptine prior to treatment with cabergoline. Four patients were men, and two were women. At the time of diagnosis, ages ranged from 9 to 62 years. Initial prolactin concentrations ranged from 430 to 14,992 ng/mL and in the last assessment ranged from 29.6 to 2,169 ng/mL. The tumor volume ranged from 0.77 to 24.0 mm. Tumor regression occurred in all patients, ranging from 20 to 100%, but total disappearance of the adenoma with an empty sella occurred in one patient. The maximum weekly doses of cabergoline ranged from 3.0 to 4.5 mg. Follow-up time ranged from seven to 17 years. Normalization of prolactin concentrations occurred only in one woman after 17 years of treatment. Three patients also underwent surgery, but only one woman was cured of the disease. This study confirms that tumors resistant to dopamine agonists are more aggressive, since we did not have any microadenoma; treatment with high dose of cabergoline may reduce the size of the tumor without its disappearance, and that normalization of prolactin concentration rarely occurs. To our knowledge, this is the longest follow-up of a series of cases with resistance to dopamine agonists.

Citing Articles

Current and Perspective Approaches to the Treatment of Prolactinomas.

Tykhonova T, Barabash N, Kanishcheva O Acta Med Litu. 2024; 30(2):96-107.

PMID: 38516518 PMC: 10952428. DOI: 10.15388/Amed.2023.30.2.1.


Dopamine Agonist-Resistant Microprolactinoma-Mechanisms, Predictors and Management: A Case Report and Literature Review.

Szmygin H, Szydelko J, Matyjaszek-Matuszek B J Clin Med. 2022; 11(11).

PMID: 35683457 PMC: 9181764. DOI: 10.3390/jcm11113070.


A scoping review to understand the indications, effectiveness, and limitations of cabergoline in radiological and biochemical remission of prolactinomas.

Mishra R, Konar S, Shrivastava A, Chouksey P, Raj S, Agrawal A Indian J Endocrinol Metab. 2022; 25(6):493-506.

PMID: 35355923 PMC: 8959198. DOI: 10.4103/ijem.ijem_338_21.


Predictors of dopamine agonist resistance in prolactinoma patients.

Vermeulen E, DHaens J, Stadnik T, Unuane D, Barbe K, Van Velthoven V BMC Endocr Disord. 2020; 20(1):68.

PMID: 32429916 PMC: 7236128. DOI: 10.1186/s12902-020-0543-4.


Prolactinomas in males: any differences?.

Duskin-Bitan H, Shimon I Pituitary. 2019; 23(1):52-57.

PMID: 31802331 DOI: 10.1007/s11102-019-01009-y.

References
1.
Roof A, Jirawatnotai S, Trudeau T, Kuzyk C, Wierman M, Kiyokawa H . The Balance of PI3K and ERK Signaling Is Dysregulated in Prolactinoma and Modulated by Dopamine. Endocrinology. 2018; 159(6):2421-2434. PMC: 6172703. DOI: 10.1210/en.2017-03135. View

2.
Beck-Peccoz P, Amr S, Faglia G, Weintraub B . Decreased receptor binding of biologically inactive thyrotropin in central hypothyroidism. Effect of treatment with thyrotropin-releasing hormone. N Engl J Med. 1985; 312(17):1085-90. DOI: 10.1056/NEJM198504253121703. View

3.
Vilar L, Abucham J, Albuquerque J, Araujo L, Azevedo M, Boguszewski C . Controversial issues in the management of hyperprolactinemia and prolactinomas - An overview by the Neuroendocrinology Department of the Brazilian Society of Endocrinology and Metabolism. Arch Endocrinol Metab. 2018; 62(2):236-263. PMC: 10118988. DOI: 10.20945/2359-3997000000032. View

4.
Prior J, Cox T, Fairholm D, Kostashuk E, Nugent R . Testosterone-related exacerbation of a prolactin-producing macroadenoma: possible role for estrogen. J Clin Endocrinol Metab. 1987; 64(2):391-4. DOI: 10.1210/jcem-64-2-391. View

5.
Gillam M, Middler S, Freed D, Molitch M . The novel use of very high doses of cabergoline and a combination of testosterone and an aromatase inhibitor in the treatment of a giant prolactinoma. J Clin Endocrinol Metab. 2002; 87(10):4447-51. DOI: 10.1210/jc.2002-020426. View