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©2014 Baishideng Publishing Group Inc.
World J Hepatol. Sep 27, 2014; 6(9): 670-676
Published online Sep 27, 2014. doi: 10.4254/wjh.v6.i9.670
Published online Sep 27, 2014. doi: 10.4254/wjh.v6.i9.670
Variables | Univariate | Multivariate | ||
HR(95%CI) | P value | HR(95%CI) | P value | |
Gender, male (vs female) | 0.384 (0.147-1.005) | 0.051 | ||
Age, ≤ 70 yr (vs > 70 yr) | 0.491 (0.225-1.071) | 0.074 | 0.354 (0.135-0.933) | 0.036 |
Previous therapy yes (vs no) | 0.035 (0.128-0.961) | 0.042 | ||
DCP, ≤ 1000 mAU/mL (vs > 1000 mAU/mL) | 0.416 (0.178-0.974) | 0.043 | ||
Initial dose of sorafenib, 800 mg (vs < 800 mg) | 0.405 (0.185-0.888) | 0.024 | ||
Adverse events > grade 2 | ||||
Anorexia - (vs +) | 0.374 (0.158-0.888) | 0.026 | ||
Skin toxicitya + (vs -) | 0.278 (0.122-0.635) | 0.002 | 0.267 (0.102-0.701) | 0.007 |
Fatigue - (vs +) | 0.404 (0.176-0.924) | 0.032 | ||
Hypoalbuminemia - (vs +) | 0.379 (0.170-0.842) | 0.017 | 0.221 (0.085-0.575) | 0.002 |
- Citation: Shomura M, Kagawa T, Shiraishi K, Hirose S, Arase Y, Koizumi J, Mine T. Skin toxicity predicts efficacy to sorafenib in patients with advanced hepatocellular carcinoma. World J Hepatol 2014; 6(9): 670-676
- URL: https://www.wjgnet.com/1948-5182/full/v6/i9/670.htm
- DOI: https://dx.doi.org/10.4254/wjh.v6.i9.670