2015
Efficacy of bevacizumab and chemotherapy in the first-line treatment of metastatic colorectal cancer: broadening KRAS-focused clinical view
BENCSIKOVÁ, Beatrix, Zbyněk BORTLÍČEK, Jana HALÁMKOVÁ, Lenka OSTRIZKOVA, Igor KISS et. al.Základní údaje
Originální název
Efficacy of bevacizumab and chemotherapy in the first-line treatment of metastatic colorectal cancer: broadening KRAS-focused clinical view
Autoři
BENCSIKOVÁ, Beatrix (703 Slovensko, garant), Zbyněk BORTLÍČEK (203 Česká republika, domácí), Jana HALÁMKOVÁ (203 Česká republika), Lenka OSTRIZKOVA (203 Česká republika), Igor KISS (203 Česká republika), Bohuslav MELICHAR (203 Česká republika), Tomáš PAVLÍK (203 Česká republika, domácí), Ladislav DUŠEK (203 Česká republika, domácí), Dalibor VALÍK (203 Česká republika), Rostislav VYZULA (203 Česká republika) a Lenka ZDRAŽILOVÁ DUBSKÁ (203 Česká republika, domácí)
Vydání
BMC Gastroenterology, LONDON, BioMed Central, 2015, 1471-230X
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30200 3.2 Clinical medicine
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 2.101
Kód RIV
RIV/00216224:14110/15:00084399
Organizační jednotka
Lékařská fakulta
UT WoS
000351720700001
Klíčová slova anglicky
Colorectal cancer; Angiogenesis inhibitors; Bevacizumab; KRAS; Biomarkers; Antineoplastic agents; Clinical practice
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 26. 10. 2017 14:58, Soňa Böhmová
Anotace
V originále
Background: The aim of the present retrospective study was to analyze clinical outcome and risk factors associated with treatment outcomes according to KRAS status in patient with metastatic colorectal cancer (mCRC) treated with bevacizumab (bev) plus chemotherapy in the first-line setting. Methods: We performed observational study on 1622 patients with mCRC treated with bev plus oxaliplatin- or irinotecan-based chemotherapy, and correlated treatment outcomes with KRAS mutation status. The primary endpoint was progression-free survival (PFS) and additionally overall survival (OS). Adverse events of bevacizumab and risk factors including location of metastases were evaluated. Results: Mutation in KRAS was present in 40.6% of mCRC cases. The median PFS in patients with wild-type KRAS (wtKRAS) vs mutant KRAS was 11.5 vs 11.4 months, respectively. The median OS was 30.7 vs 28.4 months (p = 0.312). Patients with KRAS mutation had lung metastases more frequently than wtKRAS individuals (32.0% vs 23.8%; p = 0.001). We observed no difference in clinical outcome between hepatic and extrahepatic metastatic disease. Conclusion: KRAS mutation does not interfere with clinical benefit from first-line treatment with bevacizumab plus chemotherapy in mCRC patients.