Skip to main content
. 2014 Nov 6;112(2):296–305. doi: 10.1038/bjc.2014.564

Table 2. Incidence and relative risk of all-grade QTc interval prolongation associated with VEGFR TKIs stratified by drug.

 
 
 
Incidence
 
 
Type of drug Number of studies Number of events/sample size TKI; Control VEGFR TKIs % (95% CI) Control % (95% CI) Relative risk (95% CI) P-value
Overall
18
165/3737; 7/2811
4.9 (2.9–7.9)
0.9 (0.5–1.5)
8.66 (4.92–15.2)
<0.001
Vandetanib
13
154/2432; 7/1772
8.0 (5.0–12.7)
1.2 (0.6–2.2)
9.63 (5.14–18.0)
<0.001
 100 mg
7
25/1141; 4/1155
3.6 (1.6–7.5)
1.5 (0.6–3.3)
4.83 (1.94–12.0)
0.001
 300 mg
11
129/1291; 7/809
12.2 (8.3–17.7)
1.5 (0.8–2.8)
10.6 (5.31–21.2)
<0.001
Sunitinib
2
8/455; 0/455
2.0 (1.0–3.8)
0.2 (0.0–1.6)
9.01 (1.15–70.7)
0.04
Pazopanib
2
2/536; 0/268
0.4 (0.1–1.5)
0.4 (0.0–2.6)
1.51 (0.16–14.4)
0.72
Axitiniba 1 1/314; 0/316 0.3 (0.04–2.2) 0.2 (0.0–2.4) 3.02 (0.12–73.8) 0.50

Abbreviations: CI=confidence interval; TKI=tyrosine kinase inhibitor; VEGFR=vascular endothelial growth factor receptor.

a

Only one trial is available, and we thus did not conduct a meta-analysis for axitinib.