Skip to main content

Table 2 Comparative efficacy and safety between infliximab and vedolizumab in patients with ulcerative colitis

From: Comparative efficacy and safety of infliximab and vedolizumab therapy in patients with inflammatory bowel disease: a systematic review and meta-analysis

Outcome

Treatment

Participants, N

Infliximab and biosimilars, estimate (95% CI)a

Heterogeneity (%)

Efficacy: Induction phase (Week 6)

Clinical responseb

Infliximab

242

67% (61%, 73%)

0

 

Vedolizumab

608

52% (46%, 58%)

78

Mucosal healing

Infliximab

242

61% (55%, 67%)

0

Clinical remissionb

Infliximab

242

36% (31%, 43%)

0

 

Vedolizumab

608

21% (16%, 28%)

82

Efficacy: Maintenance phase (Week 50 to 54)

Clinical responseb

Infliximab

198

54% (43%, 65%)

62

 

Vedolizumab

282

63% (56%, 69%)

51

Mucosal healing

Infliximab

198

49% (43%, 56%)

2

 

Vedolizumab

665

49% (42%, 57%)

78

Clinical remissionb

Infliximab

198

43% (33%, 54%)

60

 

Vedolizumab

665

39% (33%, 46%)

73

Safety (≤ 1 year)

Any AE

Infliximab

214

75% (60%, 86%)

86

 

Vedolizumab

543

64% (60%, 68%)

44

Any SAE

Infliximab

214

12% (6%, 23%)

72

 

Vedolizumab

543

11% (9%, 14%)

0

Any infection

Infliximab

214

21% (8%, 43%)

91

 

Vedolizumab

543

26% (22%, 29%)

14

Any serious infection

Infliximab

242

2% (1%, 5%)

0

 

Vedolizumab

489

2% (1%, 3%)

0

Discontinuation due to AE

Infliximab

214

4% (1%, 14%)

0

 

Vedolizumab

667

5% (3%, 7%)

0

Discontinuation due to lack of efficacy

Vedolizumab

667

15% (10%, 22%)

82

  1. a Random-effects model
  2. b Based on total Mayo score
  3. All results reported as the proportion of patients achieving the response
  4. AE Adverse event, CDAI Crohn’s disease activity index, CI Confidence interval, SAE Serious adverse event