J 2012

Skin toxicity and efficacy of sunitinib and sorafenib in metastatic renal cell carcinoma: a national registry-based study

POPRACH, Alexandr; Tomáš PAVLÍK; Bohuslav MELICHAR; Igor PUZANOV; Ladislav DUŠEK et al.

Základní údaje

Originální název

Skin toxicity and efficacy of sunitinib and sorafenib in metastatic renal cell carcinoma: a national registry-based study

Autoři

POPRACH, Alexandr; Tomáš PAVLÍK; Bohuslav MELICHAR; Igor PUZANOV; Ladislav DUŠEK; Zbyněk BORTLÍČEK; Rostislav VYZULA; Jitka ABRAHÁMOVÁ a Tomáš BÜCHLER

Vydání

Annals of Oncology, 2012, 0923-7534

Další údaje

Jazyk

angličtina

Typ výsledku

Článek v odborném periodiku

Obor

30200 3.2 Clinical medicine

Stát vydavatele

Česká republika

Utajení

není předmětem státního či obchodního tajemství

Odkazy

Impakt faktor

Impact factor: 7.384

Označené pro přenos do RIV

Ano

Kód RIV

RIV/00216224:14110/12:00062517

Organizační jednotka

Lékařská fakulta

UT WoS

000311642100021

Klíčová slova anglicky

hand–foot syndrome; rash; renal cell cancer; sorafenib; sunitinib; survival
Změněno: 22. 4. 2013 23:42, Ing. Mgr. Věra Pospíšilíková

Anotace

V originále

Background: A retrospective, registry-based analysis to assess the outcomes of metastatic renal cell cancer (mRCC) patients treated with sunitinib and sorafenib who developed dermatologic adverse events was performed. Patients and Methods: Data on mRCC patients treated with sunitinib or sorafenib were obtained from the Czech Clinical Registry of Renal Cell Cancer Patients. Outcomes of patients who developed hand–foot syndrome (HFS) of any grade and/or grade 3/4 rash during the treatment were compared with patients without HFS and no, mild, or moderate rash. Results: The cohort included 705 patients treated with sunitinib and 365 patients treated with sorafenib. For sunitinib, the median overall survival (OS) was 43.0 months versus 31.0 months (P = 0.027) and median progression-free survival (PFS) 20.8 months versus 11.1 months (P = 0.007) for patients with versus without dermatologic toxicity, respectively. For sorafenib, the median OS and PFS were 27.9 and 24.6 months (P = 0.244), and 12.2 and 8.8 months (P = 0.050), respectively. In multivariable Cox regression, the skin toxicity was significantly associated with longer OS in the sunitinib cohort. Conclusion: The presence of skin toxicity is associated with improved OS and PFS in patients with mRCC treated with sunitinib.