2015
Efficacy of sunitinib in patients with metastatic or unresectable renal cell carcinoma and renal insufficiency
POPRACH, Alexandr; Zbyněk BORTLÍČEK; Bohuslav MELICHAR; Radek LAKOMÝ; Marek SVOBODA et al.Základní údaje
Originální název
Efficacy of sunitinib in patients with metastatic or unresectable renal cell carcinoma and renal insufficiency
Autoři
POPRACH, Alexandr; Zbyněk BORTLÍČEK; Bohuslav MELICHAR; Radek LAKOMÝ; Marek SVOBODA; Igor KISS; Milada ZEMANOVA; Ondrej FIALA; Katerina KUBACKOVA; Oldřich COUFAL; Tomáš PAVLÍK; Ladislav DUŠEK; Rostislav VYZULA a Tomas BUCHLER
Vydání
European Journal of Cancer, Oxford, Elsevier Science Inc. 2015, 0959-8049
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: 6.163
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/15:00083158
Organizační jednotka
Lékařská fakulta
UT WoS
000350915600008
EID Scopus
2-s2.0-84924964933
Klíčová slova anglicky
Renal insufficiency; Renal cell carcinoma; Sunitinib; Survival; Treatment duration
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 19. 6. 2015 12:04, Soňa Böhmová
Anotace
V originále
Aim: The aim of this retrospective, registry-based study was to analyse treatment outcomes in patients with metastatic renal cell carcinoma (mRCC) treated with sunitinib and renal insufficiency (RI). Methods: The cohort included 790 patients treated with sunitinib between 2006 and 2013. At the start of sunitinib therapy 22, 234, and 534 patients had severe (glomerular filtration rate [GFR] <30 ml/min/1.73 m(2)), moderate (GFR 30-60 ml/min/1.73 m(2)) or mild RI/normal renal function (GFR >60 ml/min/1.73 m(2)), respectively. Results: For the three groups defined above, median progression-free survival (PFS) (95% confidence interval [CI]) was 5.3 months (0.1-18.5), 8.1 months (6.2-9.9) and 11.3 months (9.4-13.2) (p = 0.244), and median overall survival (OS) was 26.3 months (1.2-51.4), 21.2 months (13.2-29.1) and 26.3 months (22.6-29.9) (p = 0.443), respectively. The disease control rates were 45.5%, 56.4% and 59.2%, respectively (p = 0.374). No unexpected toxicity was reported in the patients with RI, but the treatment was more frequently discontinued because of adverse events and the duration of therapy was significantly shorter in these patients (p = 0.007). Conclusions: Duration of first-line targeted treatment for mRCC was significantly shorter for patients with RI, and may have translated into a trend to shorter PFS. These results highlight the need for optimal management of side-effects in patients with mRCC and RI.