Pregled bibliografske jedinice broj: 619530
Imatinib u liječenju gastrointestinalnih stromalnih tumora - iskustva KBC-a Zagreb
Imatinib u liječenju gastrointestinalnih stromalnih tumora - iskustva KBC-a Zagreb // Liječnički vjesnik : glasilo Hrvatskoga liječničkog zbora, 128 (2006), 5-6; 161-166 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 619530 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Imatinib u liječenju gastrointestinalnih stromalnih
tumora - iskustva KBC-a Zagreb
(Imatinib in gastrointestinal stromal tumor
treatment - results from University Hospital
Centre Zagreb)
Autori
Vrbanec, Damir ; Petricević, Branka ; Majerović, Mate ; Stern-Padovan, Ranka ; Belev, Borislav ; Skegro, Mate ; Herceg, Davorin ; Plestina, Stjepko ; Dedić Plavetić, Natalija ; Jakić-Razumović, Jasminka
Izvornik
Liječnički vjesnik : glasilo Hrvatskoga liječničkog zbora (0024-3477) 128
(2006), 5-6;
161-166
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
imatinib ; gastrointestinalni stromalni tumpr
(imatinib ; gastrointestinal stromal tumour)
Sažetak
Gastrointestinal stromal tumours (GIST) may be defined as intraabdominal mesenchymal tumours that express KIT protein or have an activating mutation in class III receptor tyrosine kinase gene (KIT or PDGFRalpha). Most GISTs respond to imatinib mesylate, which selectively inhibits both KIT and PDGFRalpha, and is now considered standard systemic therapy for advanced GIST. We assessed the antitumour response of patients treated with imatinib mesylate who had advanced and/or metastatic (GIST). In the Department of Medical Oncology fourteen (14) patients with advanced GIST were treated in the period from year 2002 to 2004. Imatinib mesylate was applied at the dose of 400 mg daily. Only two patients required dose enlargement up to 800 mg. All tumours had positive immunohystochemical expression of KIT. Median age of patients was 56 years. 12 male patients and 2 female patient was treated. Considering primary site of tumour we had 6 small intestine, 4 mesenterium and 4 gastric tumours. Mean duration of the treatment was 14 months (5 to 30 months). Six patients had partial remission, six had stable disease and two progression. Complete remission has not been achieved in any patient. Side-effects were mild and no patient required dose reduction or treatment discontinuation. Our results show the effectivness of targeted antitumour therapy with imatinib mesylate in advanced and/or metastatic GIST, and correspond to those in literature.
Izvorni jezik
Hrvatski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Klinički bolnički centar Zagreb
Profili:
Stjepko Pleština
(autor)
Branka Petričević
(autor)
Borislav Belev
(autor)
Davorin Herceg
(autor)
Ranka Štern-Padovan
(autor)
Mate Škegro
(autor)
Damir Vrbanec
(autor)
Jasminka Jakić-Razumović
(autor)
Natalija Dedić-Plavetić
(autor)
Mate Majerović
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Scopus
- MEDLINE