Treatment of Prolactinoma

Prolactinomas are the commonest form of pituitary neuroendocrine tumor (PitNET), representing approximately half of such tumors. Dopamine agonists (DAs) have traditionally been the primary treatment for the majority of prolactinomas, with surgery considered the second line. The aim of this review is...

Full description

Bibliographic Details
Main Authors: Warrick J. Inder, Christina Jang
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Medicina
Subjects:
Online Access:https://www.mdpi.com/1648-9144/58/8/1095
_version_ 1797431963808694272
author Warrick J. Inder
Christina Jang
author_facet Warrick J. Inder
Christina Jang
author_sort Warrick J. Inder
collection DOAJ
description Prolactinomas are the commonest form of pituitary neuroendocrine tumor (PitNET), representing approximately half of such tumors. Dopamine agonists (DAs) have traditionally been the primary treatment for the majority of prolactinomas, with surgery considered the second line. The aim of this review is to examine the historical and modern management of prolactinomas, including medical therapy with DAs, transsphenoidal surgery, and multimodality therapy for the treatment of aggressive prolactinomas and metastatic PitNETs, with an emphasis on the efficacy, safety, and future directions of current therapeutic modalities. DAs have been the mainstay of prolactinoma management since the 1970s, initially with bromocriptine and more recently with cabergoline. Cabergoline normalizes prolactin in up to 85% of patients and causes tumor shrinkage in up to 80%. Primary surgical resection of microprolactinomas and enclosed macroprolactinomas performed by experienced pituitary neurosurgeons have similar remission rates to cabergoline. Aggressive prolactinomas and metastatic PitNETS should receive multimodality therapy including high dose cabergoline, surgery, radiation therapy (preferably using stereotactic radiosurgery where suitable), and temozolomide. DAs remain a reliable mode of therapy for most prolactinomas but results from transsphenoidal surgery in expert hands have improved considerably over the last one to two decades. Surgery should be strongly considered as primary therapy, particularly in the setting of microprolactinomas, non-invasive macroprolactinomas, or prior to attempting pregnancy, and has an important role in the management of DA resistant and aggressive prolactinomas.
first_indexed 2024-03-09T09:52:55Z
format Article
id doaj.art-77baf5c15bbc4aae93541875a8e966b0
institution Directory Open Access Journal
issn 1010-660X
1648-9144
language English
last_indexed 2024-03-09T09:52:55Z
publishDate 2022-08-01
publisher MDPI AG
record_format Article
series Medicina
spelling doaj.art-77baf5c15bbc4aae93541875a8e966b02023-12-01T23:58:47ZengMDPI AGMedicina1010-660X1648-91442022-08-01588109510.3390/medicina58081095Treatment of ProlactinomaWarrick J. Inder0Christina Jang1Department of Diabetes and Endocrinology, Princess Alexandra Hospital, Woolloongabba 4102, AustraliaDepartment of Endocrinology and Diabetes, Royal Brisbane and Women’s Hospital, Herston 4029, AustraliaProlactinomas are the commonest form of pituitary neuroendocrine tumor (PitNET), representing approximately half of such tumors. Dopamine agonists (DAs) have traditionally been the primary treatment for the majority of prolactinomas, with surgery considered the second line. The aim of this review is to examine the historical and modern management of prolactinomas, including medical therapy with DAs, transsphenoidal surgery, and multimodality therapy for the treatment of aggressive prolactinomas and metastatic PitNETs, with an emphasis on the efficacy, safety, and future directions of current therapeutic modalities. DAs have been the mainstay of prolactinoma management since the 1970s, initially with bromocriptine and more recently with cabergoline. Cabergoline normalizes prolactin in up to 85% of patients and causes tumor shrinkage in up to 80%. Primary surgical resection of microprolactinomas and enclosed macroprolactinomas performed by experienced pituitary neurosurgeons have similar remission rates to cabergoline. Aggressive prolactinomas and metastatic PitNETS should receive multimodality therapy including high dose cabergoline, surgery, radiation therapy (preferably using stereotactic radiosurgery where suitable), and temozolomide. DAs remain a reliable mode of therapy for most prolactinomas but results from transsphenoidal surgery in expert hands have improved considerably over the last one to two decades. Surgery should be strongly considered as primary therapy, particularly in the setting of microprolactinomas, non-invasive macroprolactinomas, or prior to attempting pregnancy, and has an important role in the management of DA resistant and aggressive prolactinomas.https://www.mdpi.com/1648-9144/58/8/1095prolactinomadopamine agonisttranssphenoidal surgerytemozolomidestereotactic radiosurgery
spellingShingle Warrick J. Inder
Christina Jang
Treatment of Prolactinoma
Medicina
prolactinoma
dopamine agonist
transsphenoidal surgery
temozolomide
stereotactic radiosurgery
title Treatment of Prolactinoma
title_full Treatment of Prolactinoma
title_fullStr Treatment of Prolactinoma
title_full_unstemmed Treatment of Prolactinoma
title_short Treatment of Prolactinoma
title_sort treatment of prolactinoma
topic prolactinoma
dopamine agonist
transsphenoidal surgery
temozolomide
stereotactic radiosurgery
url https://www.mdpi.com/1648-9144/58/8/1095
work_keys_str_mv AT warrickjinder treatmentofprolactinoma
AT christinajang treatmentofprolactinoma