Cargando…

SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline

Background: Giant prolactinomas (GPs) are rare representing 2-3% of prolactinomas and only ~ 0.5% of all pituitary tumors. Various definitions have been proposed for GP but commonly accepted criteria is tumor dimension of ≥4 cm. GP is often associated with very high prolactin (PRL) ranging 1,000 -10...

Descripción completa

Detalles Bibliográficos
Autores principales: Madan Paramasivan, Ameena, Marouf, Sarah, Raghunathan, Sapna, Shoakazemi, Alireza, Pollock, Jonathan, Chawda, Sanjiv, Stojanovic, Nemanja, Drincic, Andjela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552231/
http://dx.doi.org/10.1210/js.2019-SAT-474
_version_ 1783424554973003776
author Madan Paramasivan, Ameena
Marouf, Sarah
Raghunathan, Sapna
Shoakazemi, Alireza
Pollock, Jonathan
Chawda, Sanjiv
Stojanovic, Nemanja
Drincic, Andjela
author_facet Madan Paramasivan, Ameena
Marouf, Sarah
Raghunathan, Sapna
Shoakazemi, Alireza
Pollock, Jonathan
Chawda, Sanjiv
Stojanovic, Nemanja
Drincic, Andjela
author_sort Madan Paramasivan, Ameena
collection PubMed
description Background: Giant prolactinomas (GPs) are rare representing 2-3% of prolactinomas and only ~ 0.5% of all pituitary tumors. Various definitions have been proposed for GP but commonly accepted criteria is tumor dimension of ≥4 cm. GP is often associated with very high prolactin (PRL) ranging 1,000 -100,000 ng/ml, significant extrasellar extension and no concomitant growth hormone or ACTH secretion. Patients predominantly present with neurological symptoms rather than endocrine dysfunction, and so the primary goal of treatment is amelioration of neurological symptoms. The literature search reveals approximately 190 papers on this topic and most are single case reports or series describing only unusual clinical manifestations. Hence, evidence based recommendations for treatment are lacking. Dopamine agonist (DA) is considered first line of therapy, as these tumors are highly sensitive to medical therapy. Surgery and radiation may be warranted in special situations. Low starting doses of cabergoline (CAB) are generally recommended due to concern for complications of apoplexy and cerebrospinal fluid (CSF) leak from rapid tumor shrinkage. However, no recommendations for a specific starting dose exist. Objective: Individual tumor and hormonal response were assessed on 15 patients (pts) with GP on low dose CAB; 0.25-0.5 mg weekly to determine the effectiveness of DA therapy. Methods: 15 GP pts from two tertiary care centers, meeting the diagnostic criteria mentioned above, were reviewed. Reduction in tumor volume and maximal tumor diameter along with PRL, after initiation of CAB, at or before 6 months and 1 year post diagnosis, was calculated. Results: Presenting symptom: visual disturbance (56%), headache (20%), apoplexy (13%) and incidental finding (6%). Mean age at diagnosis: 61 years. Male to Female: 4: 1. Basal prolactin concentration: >2000 ng/dl (12/15pts), and > 900 ng/ml (2/15). Initial total CAB dose/week: 0.25-0.5 mg (13/15) and 1-2 mg (2/15). Cranial surgery: 4/15. Complications: CSF leak (1/15). Tumor volume assessed at 6 months (11/15) and 1 year (4/15) along with decrease in maximum tumor diameter in the same period of time. PRL assessed at or before 6 months (13/15) and at 1 year (2/15). Improvement in tumor size occurred promptly even with low dose CAB (0.25-0.5mg/week). 100% of patients initiated on low dose CAB responded to therapy. Mean reduction in tumor volume at or before 6 months was 47% in 11/15, and 52% at 1 year (10/15). Mean decrease in maximal tumor dimension was calculated as 0.95 cm at 6 months (12/15) and 1.4 cm at 1 year (9/15). The overall prolactin response rate at or before 6 months was > 90% in 7/15 patients (53%) and >50% in 11/15 patients (73%). Conclusion: Our data confirms excellent tumor response to low dose cabergoline therapy. Dose as low at 0.25 mg twice weekly is proven to be effective, leading to decrease in both tumor volume and PRL levels.
format Online
Article
Text
id pubmed-6552231
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Endocrine Society
record_format MEDLINE/PubMed
spelling pubmed-65522312019-06-13 SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline Madan Paramasivan, Ameena Marouf, Sarah Raghunathan, Sapna Shoakazemi, Alireza Pollock, Jonathan Chawda, Sanjiv Stojanovic, Nemanja Drincic, Andjela J Endocr Soc Neuroendocrinology and Pituitary Background: Giant prolactinomas (GPs) are rare representing 2-3% of prolactinomas and only ~ 0.5% of all pituitary tumors. Various definitions have been proposed for GP but commonly accepted criteria is tumor dimension of ≥4 cm. GP is often associated with very high prolactin (PRL) ranging 1,000 -100,000 ng/ml, significant extrasellar extension and no concomitant growth hormone or ACTH secretion. Patients predominantly present with neurological symptoms rather than endocrine dysfunction, and so the primary goal of treatment is amelioration of neurological symptoms. The literature search reveals approximately 190 papers on this topic and most are single case reports or series describing only unusual clinical manifestations. Hence, evidence based recommendations for treatment are lacking. Dopamine agonist (DA) is considered first line of therapy, as these tumors are highly sensitive to medical therapy. Surgery and radiation may be warranted in special situations. Low starting doses of cabergoline (CAB) are generally recommended due to concern for complications of apoplexy and cerebrospinal fluid (CSF) leak from rapid tumor shrinkage. However, no recommendations for a specific starting dose exist. Objective: Individual tumor and hormonal response were assessed on 15 patients (pts) with GP on low dose CAB; 0.25-0.5 mg weekly to determine the effectiveness of DA therapy. Methods: 15 GP pts from two tertiary care centers, meeting the diagnostic criteria mentioned above, were reviewed. Reduction in tumor volume and maximal tumor diameter along with PRL, after initiation of CAB, at or before 6 months and 1 year post diagnosis, was calculated. Results: Presenting symptom: visual disturbance (56%), headache (20%), apoplexy (13%) and incidental finding (6%). Mean age at diagnosis: 61 years. Male to Female: 4: 1. Basal prolactin concentration: >2000 ng/dl (12/15pts), and > 900 ng/ml (2/15). Initial total CAB dose/week: 0.25-0.5 mg (13/15) and 1-2 mg (2/15). Cranial surgery: 4/15. Complications: CSF leak (1/15). Tumor volume assessed at 6 months (11/15) and 1 year (4/15) along with decrease in maximum tumor diameter in the same period of time. PRL assessed at or before 6 months (13/15) and at 1 year (2/15). Improvement in tumor size occurred promptly even with low dose CAB (0.25-0.5mg/week). 100% of patients initiated on low dose CAB responded to therapy. Mean reduction in tumor volume at or before 6 months was 47% in 11/15, and 52% at 1 year (10/15). Mean decrease in maximal tumor dimension was calculated as 0.95 cm at 6 months (12/15) and 1.4 cm at 1 year (9/15). The overall prolactin response rate at or before 6 months was > 90% in 7/15 patients (53%) and >50% in 11/15 patients (73%). Conclusion: Our data confirms excellent tumor response to low dose cabergoline therapy. Dose as low at 0.25 mg twice weekly is proven to be effective, leading to decrease in both tumor volume and PRL levels. Endocrine Society 2019-04-30 /pmc/articles/PMC6552231/ http://dx.doi.org/10.1210/js.2019-SAT-474 Text en Copyright © 2019 Endocrine Society https://creativecommons.org/licenses/by-nc-nd/4.0/ This article has been published under the terms of the Creative Commons Attribution Non-Commercial, No-Derivatives License (CC BY-NC-ND; https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Neuroendocrinology and Pituitary
Madan Paramasivan, Ameena
Marouf, Sarah
Raghunathan, Sapna
Shoakazemi, Alireza
Pollock, Jonathan
Chawda, Sanjiv
Stojanovic, Nemanja
Drincic, Andjela
SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline
title SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline
title_full SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline
title_fullStr SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline
title_full_unstemmed SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline
title_short SAT-474 Giant Prolactinoma Case Series Assessing Response on Initial Dose of Cabergoline
title_sort sat-474 giant prolactinoma case series assessing response on initial dose of cabergoline
topic Neuroendocrinology and Pituitary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552231/
http://dx.doi.org/10.1210/js.2019-SAT-474
work_keys_str_mv AT madanparamasivanameena sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT maroufsarah sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT raghunathansapna sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT shoakazemialireza sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT pollockjonathan sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT chawdasanjiv sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT stojanovicnemanja sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline
AT drincicandjela sat474giantprolactinomacaseseriesassessingresponseoninitialdoseofcabergoline