Role of gamma knife radiosurgery in the treatment of prolactinomas
Language English Country United States Media print
Document type Journal Article
PubMed
31222579
DOI
10.1007/s11102-019-00971-x
PII: 10.1007/s11102-019-00971-x
Knihovny.cz E-resources
- Keywords
- Gamma knife radiosurgery, Hypopituitarism, Prolactinoma, Resistance,
- MeSH
- Dopamine Agonists therapeutic use MeSH
- Adult MeSH
- Hemianopsia radiotherapy MeSH
- Hypopituitarism radiotherapy MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Prolactinoma drug therapy radiotherapy MeSH
- Radiosurgery methods MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Dopamine Agonists MeSH
PURPOSE: Stereotactic radiosurgery is one of the treatment options for prolactinomas, the most commonly used being Gamma Knife Radiosurgery (GKRS). GKRS is indicated mainly in the treatment of dopamine agonist (DA)-resistant prolactinomas. In our study, we report on our experience in treating prolactinoma patients by GKRS. METHODS: Twenty-eight patients were followed-up after GKRS for 26-195 months (median 140 months). Prior to GKRS, patients were treated with DAs and 9 of them (32.1%) underwent previous neurosurgery. Cavernous sinus invasion was present in 16 (57.1%) patients. Indications for GKRS were (i) resistance to DA treatment (17 patients), (ii) drug intolerance (5 patients), or (iii) attempts to reduce the dosage and/or shorten the length of DA treatment (6 patients). RESULTS: After GKRS, normoprolactinaemia was achieved in 82.1% of patients, out of which hormonal remission (normoprolactinaemia after discontinuation of DAs) was achieved in 13 (46.4%), and hormonal control (normoprolactinaemia while taking DAs) in 10 (35.7%) patients. GKRS arrested adenoma growth or decreased adenoma size in all cases. Two patients (8.3%) developed hypopituitarism after GKRS. Prolactinoma cystic transformation with expansive behaviour, manifested by bilateral hemianopsia, was observed in one patient. CONCLUSIONS: GKRS represents an effective treatment option, particularly for DA-resistant prolactinomas. Normoprolactinaemia was achieved in the majority of patients, either after discontinuation of, or while continuing to take, DAs. Tumour growth was arrested in all cases. The risk of the development of hypopituitarism can be limited if the safe dose to the pituitary and infundibulum is maintained.
Institute of Informatics of the Czech Academy of Science Prague Czech Republic
Radiodiagnostic Department Na Homolce Hospital Prague Czech Republic
Stereotactic and Radiation Neurosurgery Na Homolce Hospital Prague Czech Republic
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Neurosurgery. 2000 Jan;46(1):138-49; discussion 150-1 PubMed
Stereotact Funct Neurosurg. 1999;72 Suppl 1:88-100 PubMed
Stereotact Funct Neurosurg. 1999;72 Suppl 1:101-10 PubMed
Stereotact Funct Neurosurg. 1999;72 Suppl 1:111-8 PubMed
J Neurosurg. 2000 Dec;93 Suppl 3:10-3 PubMed
J Neurosurg. 2000 Dec;93 Suppl 3:14-8 PubMed
J Clin Endocrinol Metab. 2001 Nov;86(11):5256-61 PubMed
J Neurosurg. 2001 Aug;95(2):285-91 PubMed
J Clin Endocrinol Metab. 2002 Feb;87(2):457-65 PubMed
J Neurosurg. 2002 Sep;97(3):525-30 PubMed
J Neurosurg. 2002 Dec;97(5 Suppl):415-21 PubMed
Neurosurgery. 2003 Feb;52(2):309-16; discussion 316-7 PubMed
Neurosurgery. 2003 Jul;53(1):51-9; discussion 59-61 PubMed
Clin Endocrinol (Oxf). 1992 Dec;37(6):534-41 PubMed
Yonsei Med J. 2003 Aug 30;44(4):602-7 PubMed
Neurosurgery. 2004 Jun;54(6):1385-93; discussion 1393-4 PubMed
J Neurosurg. 2005 Apr;102(4):678-91 PubMed
Clin Endocrinol (Oxf). 2005 Oct;63(4):450-5 PubMed
Clin Endocrinol (Oxf). 2006 May;64(5):588-95 PubMed
Endocr Rev. 2006 Aug;27(5):485-534 PubMed
Neurosurgery. 2006 Aug;59(2):255-66; discussion 255-66 PubMed
N Engl J Med. 2007 Jan 4;356(1):29-38 PubMed
N Engl J Med. 2007 Jan 4;356(1):39-46 PubMed
Eur J Endocrinol. 2007 Feb;156(2):225-31 PubMed
Clin Endocrinol (Oxf). 2009 May;70(5):732-41 PubMed
J Clin Endocrinol Metab. 2008 Dec;93(12):4721-7 PubMed
Eur J Endocrinol. 2009 May;160(5):747-52 PubMed
J Clin Endocrinol Metab. 2009 Sep;94(9):3400-7 PubMed
J Clin Endocrinol Metab. 2010 Jan;95(1):43-51 PubMed
J Neurosurg. 2011 Feb;114(2):303-9 PubMed
Neurosurgery. 2010 Jul;67(1):27-32; discussion 32-3 PubMed
Eur J Endocrinol. 2011 Feb;164(2):169-78 PubMed
J Clin Endocrinol Metab. 2011 Feb;96(2):273-88 PubMed
World Neurosurg. 2010 Jul;74(1):147-52 PubMed
Pituitary. 2013 Mar;16(1):68-75 PubMed
Eur J Endocrinol. 2012 Nov;167(5):651-62 PubMed
QJM. 2013 Jun;106(6):495-504 PubMed
Pituitary. 2015 Jun;18(3):376-84 PubMed
Pituitary. 2015 Dec;18(6):820-30 PubMed
J Neurol Surg Rep. 2015 Jul;76(1):e105-8 PubMed
Drugs. 1995 Feb;49(2):255-79 PubMed
Clin Endocrinol (Oxf). 1994 Dec;41(6):821-6 PubMed
N Engl J Med. 1994 Oct 6;331(14):904-9 PubMed
Drug Saf. 1996 Apr;14(4):228-38 PubMed
J Clin Endocrinol Metab. 1997 Mar;82(3):876-83 PubMed
Stereotact Funct Neurosurg. 1998 Oct;70 Suppl 1:95-109 PubMed