2017
Regorafenib in the Real-Life Clinical Practice: Data from the Czech Registry
KOPEČKOVÁ, Kateřina, Tomáš BÜCHLER, Zbyněk BORTLÍČEK, Karel HEJDUK, Renata CHLOUPKOVÁ et. al.Základní údaje
Originální název
Regorafenib in the Real-Life Clinical Practice: Data from the Czech Registry
Název česky
Regorafenib v reálné klinické praxi: Data z Českého registru
Autoři
KOPEČKOVÁ, Kateřina (203 Česká republika), Tomáš BÜCHLER (203 Česká republika), Zbyněk BORTLÍČEK (203 Česká republika, garant, domácí), Karel HEJDUK (203 Česká republika, domácí), Renata CHLOUPKOVÁ (203 Česká republika, domácí), Bohuslav MELICHAR (203 Česká republika), Petra POKORNÁ (203 Česká republika), Jiří TOMÁŠEK (203 Česká republika), Zdeněk LINKE (203 Česká republika), Luboš PETRUŽELKA (203 Česká republika), Igor KISS (203 Česká republika) a Jana PRAUSOVÁ (203 Česká republika)
Vydání
Targeted Oncology, Dordrecht, Springer, 2017, 1776-2596
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30204 Oncology
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 3.907
Kód RIV
RIV/00216224:14110/17:00095942
Organizační jednotka
Lékařská fakulta
UT WoS
000393121700009
Klíčová slova anglicky
Rheumatoid arthritis; Ultrasonography; Synovitis; Health assessment questionnaire
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 28. 1. 2021 11:25, Mgr. Tereza Miškechová
Anotace
V originále
Objective To describe the use of regorafenib for the treatment of metastatic colorectal cancer (mCRC) in clinical practice in the Czech Republic, and to describe the clinical outcomes of patients in terms of safety and survival. Patients and Methods The data of patients treated with regorafenib were extracted from the national CORECT registry. The CORECT registry is a non-interventional post-marketing database, gathering information about patients with CRC and treated with targeted agents. Twenty oncology centres in the Czech Republic contributed to this registry. Collected data included patients’ characteristics, disease history, cancer treatments, response to treatments and safety. Results A total of 148 patients treated with regorafenib in clinical practice were analysed. At regorafenib initiation, almost all patients were fully active or slightly restricted in physical activity. Regorafenib was not administered as first-line treatment in any patient. Median progression-free survival was 3.5 months and median overall survival was 9.3 months. One-year survival rate was 44.6 %. Four partial responses were observed and 51 stable diseases. Progression was observed in 66 patients (44.6 %). The main reported adverse events were skin toxicity (5.4 %) and fatigue (2.0 %). Conclusions Regorafenib is a well-established treatment for pretreated patients with mCRC, however real-life data are scarce. Our results demonstrated slightly better efficacy of regorafenib and better safety profile in patients with mCRC compared to the randomised trials.
Návaznosti
LM2015090, projekt VaV |
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