The clinical and therapeutic profiles of prolactinomas associated with germline pathogenic variants in the
AIP
MEN1
cabergoline
dopamine agonist
genetic
prolactinoma
resistance
Journal
Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782
Informations de publication
Date de publication:
2023
2023
Historique:
received:
19
06
2023
accepted:
17
07
2023
medline:
18
9
2023
pubmed:
15
9
2023
entrez:
15
9
2023
Statut:
epublish
Résumé
Prolactinomas are the most frequent type of pituitary adenoma encountered in clinical practice. Dopamine agonists (DA) like cabergoline typically provide sign/ symptom control, normalize prolactin levels and decrease tumor size in most patients. DA-resistant prolactinomas are infrequent and can occur in association with some genetic causes like MEN1 and pathogenic germline variants in the We compared the clinical, radiological, and therapeutic characteristics of AIPvar-related prolactinomas (n=13) with unselected hospital-treated prolactinomas ("unselected", n=41) and genetically-negative, DA-resistant prolactinomas (DA-resistant, n=39). AIPvar-related prolactinomas occurred at a significantly younger age than the unselected or DA-resistant prolactinomas (p<0.01). Males were more common in the AIPvar (75.0%) and DA- resistant (49.7%) versus unselected prolactinomas (9.8%; p<0.001). AIPvar prolactinomas exhibited significantly more frequent invasion than the other groups (p<0.001) and exhibited a trend to larger tumor diameter. The DA-resistant group had significantly higher prolactin levels at diagnosis than the AIPvar group (p<0.001). Maximum DA doses were significantly higher in the AIPvar and DA-resistant groups versus unselected. DA-induced macroadenoma shrinkage (>50%) occurred in 58.3% in the AIPvar group versus 4.2% in the DA-resistant group (p<0.01). Surgery was more frequent in the AIPvar and DA- resistant groups (43.8% and 61.5%, respectively) versus unselected (19.5%: p<0.01). Radiotherapy was used only in AIPvar (18.8%) and DA-resistant (25.6%) groups. AIPvar confer an aggressive phenotype in prolactinomas, with invasive tumors occurring at a younger age. These characteristics can help differentiate rare AIPvar related prolactinomas from DA-resistant, genetically-negative tumors.
Identifiants
pubmed: 37711900
doi: 10.3389/fendo.2023.1242588
pmc: PMC10498111
doi:
Substances chimiques
Dopamine Agonists
0
Prolactin
9002-62-4
Receptors, Aryl Hydrocarbon
0
aryl hydrocarbon receptor-interacting protein
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1242588Informations de copyright
Copyright © 2023 Vroonen, Beckers, Camby, Cuny, Beckers, Jaffrain-Rea, Cogne, Naves, Ferriere, Romanet, Elenkova, Karhu, Brue, Barlier, Pétrossians and Daly.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
J Clin Endocrinol Metab. 2015 Sep;100(9):E1242-54
pubmed: 26186299
Horm Res. 2009;71(3):132-41
pubmed: 19188737
Endocr Connect. 2017 Nov;6(8):914-925
pubmed: 29074612
J Clin Endocrinol Metab. 2010 Nov;95(11):E373-83
pubmed: 20685857
J Clin Endocrinol Metab. 1990 Dec;71(6):1427-33
pubmed: 1977759
J Clin Endocrinol Metab. 2016 Aug;101(8):3144-54
pubmed: 27253664
J Clin Endocrinol Metab. 2020 Mar 1;105(3):
pubmed: 31580439
J Clin Endocrinol Metab. 2008 Jun;93(6):2390-401
pubmed: 18381572
Endocr Relat Cancer. 2012 May 03;19(3):233-41
pubmed: 22291433
J Endocrinol Invest. 2011 Apr;34(4):312-6
pubmed: 21406957
Neuroendocrinology. 2019;109(1):42-50
pubmed: 30481756
Clin Endocrinol (Oxf). 2021 Mar;94(3):413-423
pubmed: 33340135
Medicina (B Aires). 2020;80(2):181-184
pubmed: 32282328
J Clin Endocrinol Metab. 1997 Jul;82(7):2102-7
pubmed: 9215279
J Med Genet. 2018 Aug;55(8):522-529
pubmed: 29632148
Oncogene. 2021 Nov;40(45):6354-6368
pubmed: 34588620
Int J Cancer. 2020 Dec 15;147(12):3523-3538
pubmed: 32856736
Pituitary. 2022 Dec;25(6):819-830
pubmed: 35851929
Neuroendocrinology. 2019;109(1):20-27
pubmed: 30731464
Genet Test Mol Biomarkers. 2018 Dec;22(12):702-708
pubmed: 30461320
Eur J Endocrinol. 2010 Sep;163(3):369-76
pubmed: 20530095
Lancet Diabetes Endocrinol. 2015 Nov;3(11):906-13
pubmed: 25466526
Clin Genet. 2010 Nov;78(5):457-63
pubmed: 20507346
J Neurooncol. 2014 May;117(3):421-8
pubmed: 24146188
J Clin Endocrinol Metab. 2007 May;92(5):1891-6
pubmed: 17244780
Eur J Endocrinol. 2011 Oct;165(4):509-15
pubmed: 21753072
J Clin Endocrinol Metab. 2007 May;92(5):1952-5
pubmed: 17299063
Endocrinol Metab Clin North Am. 2020 Sep;49(3):347-355
pubmed: 32741475
Eur J Endocrinol. 2013 Mar 15;168(4):533-41
pubmed: 23321498
J Clin Endocrinol Metab. 2015 Mar;100(3):1177-86
pubmed: 25532043
Eur J Endocrinol. 2013 Oct 23;169(6):867-84
pubmed: 24050928
Eur J Endocrinol. 2019 Dec;181(6):R235-R254
pubmed: 31658440
J Clin Endocrinol Metab. 2021 May 13;106(6):e2452-e2454
pubmed: 33550413
Eur J Endocrinol. 2012 Nov;167(5):651-62
pubmed: 22918301
Rev Endocr Metab Disord. 2022 Oct;23(5):1089-1099
pubmed: 36125673
Clin Endocrinol (Oxf). 2019 May;90(5):662-669
pubmed: 30818417
Pituitary. 2020 Feb;23(1):27-37
pubmed: 31522358
J Clin Endocrinol Metab. 2011 Feb;96(2):273-88
pubmed: 21296991
J Clin Endocrinol Metab. 2015 Sep;100(9):3288-96
pubmed: 26126205
Front Endocrinol (Lausanne). 2022 Jan 12;12:791633
pubmed: 35095761
J Clin Endocrinol Metab. 2006 Sep;91(9):3316-23
pubmed: 16787992
Eur J Endocrinol. 2014 Nov;171(5):659-66
pubmed: 25184284
Proc Natl Acad Sci U S A. 2007 Mar 6;104(10):4101-5
pubmed: 17360484
Pituitary. 2021 Feb;24(1):48-52
pubmed: 33010004
Endocr Rev. 2013 Apr;34(2):239-77
pubmed: 23371967
Endocr Connect. 2019 Apr;8(4):338-348
pubmed: 30822274
Eur J Endocrinol. 2021 Aug 27;185(4):485-496
pubmed: 34313605
Best Pract Res Clin Endocrinol Metab. 2019 Apr;33(2):101290
pubmed: 31326373
J Clin Endocrinol Metab. 2002 Feb;87(2):457-65
pubmed: 11836268
Eur J Endocrinol. 2021 Nov 26;185(6):863-873
pubmed: 34636744
J Clin Endocrinol Metab. 2012 Apr;97(4):E663-70
pubmed: 22319033