Literature DB >> 16411068

Pharmacologic resistance in prolactinoma patients.

Mark E Molitch1.   

Abstract

Pharmacologic resistance to dopamine agonists is defined here as failure to normalize PRL levels and failure to decrease macroprolactinoma size by >or=50%. Failure to normalize PRL levels is found in about one-quarter of patients treated with bromocriptine and 10-15% of those treated with pergolide or cabergoline. Failure to achieve at least a 50% reduction in tumor size occurs in about one-third of those treated with bromocriptine and 10-15% of those treated with pergolide or cabergoline. The cause of dopamine resistance is primarily a decrease in D(2) receptors but the receptors have normal affinity for dopamine. Treatment approaches for patients resistant to dopamine agonists include changing to another dopamine agonist and increasing the dose of the drug as long as there is continued response to the dose increases and no adverse effects with higher doses. Transsphenoidal surgery is also an option. Clomiphene, gonadotropins, and GnRH can be used if fertility is desired. For those not desiring fertility, estrogen replacement may be used unless there is a macroadenoma, in which case control of tumor growth is also an issue and dopamine agonists are generally necessary. In many patients modest or even no reduction in tumor size may be acceptable as long as there is not tumor growth. Hormone replacement (estrogen or testosterone) may cause a decrease in efficacy of the dopamine agonist so that it must be carried out cautiously. Reduction of endogenous estrogen, use of selective estrogen receptor modulators, and aromatase inhibitors are potential experimental approaches.

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Year:  2005        PMID: 16411068     DOI: 10.1007/s11102-005-5085-2

Source DB:  PubMed          Journal:  Pituitary        ISSN: 1386-341X            Impact factor:   4.107


  110 in total

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Authors:  H G Friesen; G Tolis
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Journal:  Ann Endocrinol (Paris)       Date:  2000-11       Impact factor: 2.478

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Authors:  C Pasqualini; F Bojda; B Kerdelhué
Journal:  Endocrinology       Date:  1986-12       Impact factor: 4.736

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Journal:  J Clin Endocrinol Metab       Date:  1986-12       Impact factor: 5.958

9.  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.

Authors:  Mary P Gillam; Stewart Middler; Daniel J Freed; Mark E Molitch
Journal:  J Clin Endocrinol Metab       Date:  2002-10       Impact factor: 5.958

10.  Efficacy and safety of bromocriptine in the treatment of macroprolactinomas.

Authors:  O Essaïs; R Bouguerra; J Hamzaoui; Z Marrakchi; S Hadjri; S Chamakhi; B Zidi; C Ben Slama
Journal:  Ann Endocrinol (Paris)       Date:  2002-12       Impact factor: 2.478

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  52 in total

1.  Cabergoline for the treatment of bromocriptine-resistant invasive giant prolactinomas.

Authors:  Hai Yan Huang; Weiwei Zhai; Hao Tang; Guo Zhen Hui; Zhe Bao Wu
Journal:  Endocrine       Date:  2018-09-20       Impact factor: 3.633

2.  Treatment of multiresistant prolactinomas with a combination of cabergoline and octreotide LAR.

Authors:  Ernesto Sosa-Eroza; Etual Espinosa; Claudia Ramírez-Rentería; Victoria Mendoza; Rocío Arreola; Moises Mercado
Journal:  Endocrine       Date:  2018-06-11       Impact factor: 3.633

3.  Calcified Prolactinoma of the Pituitary Gland: Illustrative Case Reports Highlighting Medical versus Surgical Intervention.

Authors:  Sherwin Tavakol; Asma Hasan; Michelle A Wedemeyer; Joshua Bakhsheshian; Chia-Shang J Liu; Mark S Shiroishi; Anna Mathew; John D Carmichael; Gabriel Zada
Journal:  J Neurol Surg B Skull Base       Date:  2019-02-05

4.  Cabergoline and prolactinomas: lack of association between DRD2 polymorphisms and response to treatment.

Authors:  Cbf Bueno; E B Trarbach; M D Bronstein; A Glezer
Journal:  Pituitary       Date:  2017-06       Impact factor: 4.107

5.  Invasive giant prolactinoma with loss of therapeutic response to cabergoline: expression of angiogenic markers.

Authors:  María Susana Mallea-Gil; Carolina Cristina; María Inés Perez-Millan; Ana M Rodriguez Villafañe; Carolina Ballarino; Graciela Stalldecker; Damasia Becu-Villalobos
Journal:  Endocr Pathol       Date:  2009       Impact factor: 3.943

6.  Cabergoline versus bromocriptine for the treatment of giant prolactinomas: A quantitative and systematic review.

Authors:  Hai Yan Huang; Shao Jian Lin; Wei Guo Zhao; Zhe Bao Wu
Journal:  Metab Brain Dis       Date:  2018-03-15       Impact factor: 3.584

7.  Curcumin (diferuloylmethane) inhibits cell proliferation, induces apoptosis, and decreases hormone levels and secretion in pituitary tumor cells.

Authors:  Matthew Miller; Shenglin Chen; Jeffrey Woodliff; Sanjay Kansra
Journal:  Endocrinology       Date:  2008-05-01       Impact factor: 4.736

8.  Temozolomide in the treatment of an invasive prolactinoma resistant to dopamine agonists.

Authors:  Lisa M Neff; Michelle Weil; Alan Cole; Thomas R Hedges; William Shucart; Donald Lawrence; Jay-Jiguang Zhu; Arthur S Tischler; Ronald M Lechan
Journal:  Pituitary       Date:  2007       Impact factor: 4.107

9.  Enhanced nestin expression and small blood vessels in human pituitary adenomas.

Authors:  María Inés Perez-Millan; Silvia Inés Berner; Guillermina María Luque; Cristian De Bonis; Gustavo Sevlever; Damasia Becu-Villalobos; Carolina Cristina
Journal:  Pituitary       Date:  2013-09       Impact factor: 4.107

Review 10.  Pharmacotherapy for adults with tumors of the central nervous system.

Authors:  Nina F Schor
Journal:  Pharmacol Ther       Date:  2008-11-27       Impact factor: 12.310

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