Use of the Leksell gamma knife in the treatment of prolactinoma patients
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F09%3A3746" target="_blank" >RIV/00216208:11110/09:3746 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/67985807:_____/09:00337772 RIV/00064165:_____/09:3746
Výsledek na webu
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DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Use of the Leksell gamma knife in the treatment of prolactinoma patients
Popis výsledku v původním jazyce
We describe our 12-year experience in treating prolactinomas with the Leksell gamma knife (LGK). We followed 35 prolactinoma patients (25.7% microprolactinomas, 74.3% macroprolactinomas) treated with LGK irradiation. The mean follow-up period was 75.5 months. Prior to LGK irradiation, patients were treated with DA and 10 of them (28.6%) underwent neurosurgery. Indications for LGK irradiation were: DA intolerance (31.4%), DA resistance (45.7%) and efforts to reduce the DA dose or shorten the period of administration (22.9%). Pituitary function was monitored regularly at 6-month intervals. The central radiation dose range was 40-80 Gy (median 70 Gy), and the minimal peripheral dose was 20-49 Gy (median 34 Gy). Normoprolactinaemia was achieved in 37.1% ofthe patients who discontinued DA and in 42.9% of patients who continued DA treatment after LGK irradiation. No relapse was seen in any patient. The size of adenoma decreased even in those patients in whom it was not changed by previous D
Název v anglickém jazyce
Use of the Leksell gamma knife in the treatment of prolactinoma patients
Popis výsledku anglicky
We describe our 12-year experience in treating prolactinomas with the Leksell gamma knife (LGK). We followed 35 prolactinoma patients (25.7% microprolactinomas, 74.3% macroprolactinomas) treated with LGK irradiation. The mean follow-up period was 75.5 months. Prior to LGK irradiation, patients were treated with DA and 10 of them (28.6%) underwent neurosurgery. Indications for LGK irradiation were: DA intolerance (31.4%), DA resistance (45.7%) and efforts to reduce the DA dose or shorten the period of administration (22.9%). Pituitary function was monitored regularly at 6-month intervals. The central radiation dose range was 40-80 Gy (median 70 Gy), and the minimal peripheral dose was 20-49 Gy (median 34 Gy). Normoprolactinaemia was achieved in 37.1% ofthe patients who discontinued DA and in 42.9% of patients who continued DA treatment after LGK irradiation. No relapse was seen in any patient. The size of adenoma decreased even in those patients in whom it was not changed by previous D
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FB - Endokrinologie, diabetologie, metabolismus, výživa
OECD FORD obor
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Návaznosti výsledku
Projekt
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Návaznosti
Z - Vyzkumny zamer (s odkazem do CEZ)
Ostatní
Rok uplatnění
2009
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Clinical endocrinology
ISSN
0300-0664
e-ISSN
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Svazek periodika
70
Číslo periodika v rámci svazku
5
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
10
Strana od-do
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Kód UT WoS článku
000264563800012
EID výsledku v databázi Scopus
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