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. 2016 Aug 2;7(45):74303–74313. doi: 10.18632/oncotarget.11030

Table 2. Reasons of withdrawal from sorafenib*.

Total (n = 652) Sorafenib (n = 291) TACE followed by sorafenib (n = 236) TACE combined with sorafenib (n = 125) P value
Disease progression [n (%)] 421 (64.6) 193 (66.4) 163 (68.9) 65 (52.3) 0.10
Adverse drug reactions [n (%)] 87 (13.3) 38 (13.2) 22 (9.3) 27 (21.5) 0.06
Worsening liver function or death [n (%)] 6 (0.9) 4 (1.3) 0 (0.0) 2 (1.5) 0.87
Physicians' decision [n (%)] 21 (3.2) 6 (2.0) 6 (2.5) 9 (7.2) 0.08
Economic issue [n (%)] 6 (0.9) 0 (0.0) 6 (2.5) 0 (0.0) 0.07
Unknown (including loss of follow-up) [n (%)] 69 (10.6) 28 (9.6) 27 (11.5) 14 (10.8) 0.92
*

Data are presented as means ± standard deviations.

TACE, transarterial chemoembolization