Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas

Prolactinomas are the most common hypersecretory pituitary adenoma. The traditional first-line therapy is dopamine agonists (DAs), which are highly effective and tolerated in the majority of cases. However, DAs have the potential for psychiatric complications, such as psychosis, impulse control diso...

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Main Authors: Edward Mignone, Alistair K Jukes, Rowan Valentine, Richard Allison, Sunita M C De Sousa
Format: Article
Language:English
Published: Bioscientifica 2025-01-01
Series:Endocrine Oncology
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Online Access:https://eo.bioscientifica.com/view/journals/eo/5/1/EO-24-0065.xml
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author Edward Mignone
Alistair K Jukes
Rowan Valentine
Richard Allison
Sunita M C De Sousa
author_facet Edward Mignone
Alistair K Jukes
Rowan Valentine
Richard Allison
Sunita M C De Sousa
author_sort Edward Mignone
collection DOAJ
description Prolactinomas are the most common hypersecretory pituitary adenoma. The traditional first-line therapy is dopamine agonists (DAs), which are highly effective and tolerated in the majority of cases. However, DAs have the potential for psychiatric complications, such as psychosis, impulse control disorders and anxiety/depression. It has been repeatedly suggested that aripiprazole may be considered in individuals with a psychiatric disorder and prolactinoma, potentially enabling DA dose reduction or even cessation. We report the first case of aripiprazole competing with cabergoline and reducing its efficacy in the treatment of a giant prolactinoma, as evidenced by an immediate and marked rise in serum prolactin (approximately 350% increase over 5 weeks) despite stable cabergoline dosing. We also present a systematic review of aripiprazole use in prolactinomas, showing that aripiprazole monotherapy effectively reduces serum prolactin and concurrently commenced aripiprazole/DA dual therapy may still permit prolactin lowering, although there were no previous cases where aripiprazole was added to an established DA therapy to indicate the direct effect of aripiprazole on DA efficacy. Based on our case, we support close monitoring of individuals with prolactinomas on dual aripiprazole/DA therapy and recommend against the addition of aripiprazole to DA therapy where timely prolactinoma treatment is essential (e.g. aggressive prolactinomas and those associated with compressive effects).
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spelling doaj-art-c89a2c5ec86d42fbaaa67447bbe468d12025-01-12T04:28:27ZengBioscientificaEndocrine Oncology2634-47932025-01-015110.1530/EO-24-00651Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomasEdward Mignone0Alistair K Jukes1Rowan Valentine2Richard Allison3Sunita M C De Sousa4Endocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, AustraliaDepartment of Neurosurgery, Royal Adelaide Hospital, Adelaide, AustraliaDepartment of Otorhinolaryngology, Queen Elizabeth Hospital, Woodville, South Australia, AustraliaSchool of Medicine, University of Adelaide, Adelaide, South Australia, AustraliaEndocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, AustraliaProlactinomas are the most common hypersecretory pituitary adenoma. The traditional first-line therapy is dopamine agonists (DAs), which are highly effective and tolerated in the majority of cases. However, DAs have the potential for psychiatric complications, such as psychosis, impulse control disorders and anxiety/depression. It has been repeatedly suggested that aripiprazole may be considered in individuals with a psychiatric disorder and prolactinoma, potentially enabling DA dose reduction or even cessation. We report the first case of aripiprazole competing with cabergoline and reducing its efficacy in the treatment of a giant prolactinoma, as evidenced by an immediate and marked rise in serum prolactin (approximately 350% increase over 5 weeks) despite stable cabergoline dosing. We also present a systematic review of aripiprazole use in prolactinomas, showing that aripiprazole monotherapy effectively reduces serum prolactin and concurrently commenced aripiprazole/DA dual therapy may still permit prolactin lowering, although there were no previous cases where aripiprazole was added to an established DA therapy to indicate the direct effect of aripiprazole on DA efficacy. Based on our case, we support close monitoring of individuals with prolactinomas on dual aripiprazole/DA therapy and recommend against the addition of aripiprazole to DA therapy where timely prolactinoma treatment is essential (e.g. aggressive prolactinomas and those associated with compressive effects).https://eo.bioscientifica.com/view/journals/eo/5/1/EO-24-0065.xmlaripiprazoleprolactinomacabergolineneuroendocrinology
spellingShingle Edward Mignone
Alistair K Jukes
Rowan Valentine
Richard Allison
Sunita M C De Sousa
Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
Endocrine Oncology
aripiprazole
prolactinoma
cabergoline
neuroendocrinology
title Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
title_full Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
title_fullStr Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
title_full_unstemmed Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
title_short Aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
title_sort aripiprazole use as a cause of dopamine agonist failure in the treatment of prolactinomas
topic aripiprazole
prolactinoma
cabergoline
neuroendocrinology
url https://eo.bioscientifica.com/view/journals/eo/5/1/EO-24-0065.xml
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