SLABÝ, Ondřej, Milana ŠACHLOVÁ, Markéta BEDNAŘÍKOVÁ, Pavel FABIAN, Marek SVOBODA, Simona VYTOPILOVÁ, Dalibor VALÍK a Rostislav VYZULA. Gene Expression of Somatostatin Receptor 4 Predicts Clinical Outcome of Patients with Metastatic Neuroendocrine Tumors Treated with Somatostatin Analogs. Cancer Biotherapy and Radiopharmaceuticals. Mary Ann Liebert, 2010, roč. 25, č. 2, s. 237-243. ISSN 1084-9785. Dostupné z: https://dx.doi.org/10.1089/cbr.2009.0708.
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Základní údaje
Originální název Gene Expression of Somatostatin Receptor 4 Predicts Clinical Outcome of Patients with Metastatic Neuroendocrine Tumors Treated with Somatostatin Analogs
Autoři SLABÝ, Ondřej (203 Česká republika, garant, domácí), Milana ŠACHLOVÁ (203 Česká republika, domácí), Markéta BEDNAŘÍKOVÁ (203 Česká republika, domácí), Pavel FABIAN (203 Česká republika, domácí), Marek SVOBODA (203 Česká republika, domácí), Simona VYTOPILOVÁ (203 Česká republika, domácí), Dalibor VALÍK (203 Česká republika, domácí) a Rostislav VYZULA (203 Česká republika, domácí).
Vydání Cancer Biotherapy and Radiopharmaceuticals, Mary Ann Liebert, 2010, 1084-9785.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30200 3.2 Clinical medicine
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
Impakt faktor Impact factor: 1.873
Kód RIV RIV/00216224:14110/10:00051807
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1089/cbr.2009.0708
UT WoS 000277155900014
Klíčová slova anglicky carcinoid; neuroendocrine tumors; prognosis; response prediction; somatostatin analogs; somatostatin receptors
Příznaky Mezinárodní význam
Změnil Změnil: Mgr. Michal Petr, učo 65024. Změněno: 17. 4. 2012 11:11.
Anotace
Somatostatin analogs (SSA) are the standard diagnostic and treatment tools in the clinical management of patients with neuroendocrine tumors (NETs) expressing somatostatin receptors (SSTRs). Although symptomatic and biochemical control is obtained with SSA in the majority of functional NETs, antineoplastic effects of SSA are partial and of limited duration. The aim of this study was to quantify expression levels of five SSTR subtypes (SSTR1-SSTR5) and correlate them with the clinical outcomes of patients with NETs who underwent SSA therapy. The expression levels were analyzed using real-time polymerase chain reaction in a series of 22 metastatic NETs with a median time of 10 months on the SSA therapy (range 2-82 months). The median duration of disease stabilization in patients who developed progression (n=14) was 9 months (range 3-92 months). The median survival period for all patients was 44 months (range 3-175 months). According to RECIST criteria, one (5%) partial objective tumor response was obtained, disease stabilization was achieved in 10 (45%) patients, and progressive disease was observed in 11 (50%). Analysis of mRNA expression of the SSTR subtypes showed that SSTR2 and SSTR5 were expressed in all of the studied NETs; SSTR1 and SSTR4 in all but 3 tumors (86%); and SSTR3 in only 10 NETs (49%). Interestingly, our preliminary data suggest that only the levels of SSTR4, though it has the lowest affinity for SSA of all SSTR subtypes, were significantly associated with the stabilization of disease during SSA therapy ( p=0.0357). These levels correlated with time to progression ( p=0.0015) and overall survival ( p=0.0017) in NET patients.
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