Detailed Information on Publication Record
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.Basic information
Original name
Skin toxicity and efficacy of sunitinib and sorafenib in metastatic renal cell carcinoma: a national registry-based study
Authors
POPRACH, Alexandr (203 Czech Republic), Tomáš PAVLÍK (203 Czech Republic, belonging to the institution), Bohuslav MELICHAR (203 Czech Republic), Igor PUZANOV (203 Czech Republic), Ladislav DUŠEK (203 Czech Republic, belonging to the institution), Zbyněk BORTLÍČEK (203 Czech Republic, belonging to the institution), Rostislav VYZULA (203 Czech Republic, guarantor), Jitka ABRAHÁMOVÁ (203 Czech Republic) and Tomáš BÜCHLER (203 Czech Republic)
Edition
Annals of Oncology, 2012, 0923-7534
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
30200 3.2 Clinical medicine
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 7.384
RIV identification code
RIV/00216224:14110/12:00062517
Organization unit
Faculty of Medicine
UT WoS
000311642100021
Keywords in English
hand–foot syndrome; rash; renal cell cancer; sorafenib; sunitinib; survival
Změněno: 22/4/2013 23:42, Ing. Mgr. Věra Pospíšilíková
Abstract
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.