Skip to main content

Table 3 Anti-tumor activity of camrelizumab in different dosage groups

From: Safety, activity, and pharmacokinetics of camrelizumab in advanced Asian melanoma patients: a phase I study

Variables

60 mg (n = 12)

200 mg (n = 12)

400 mg (n = 12)

Total (n = 36)

Best response, n (%)

 PR

1 (8.3)

1 (8.3)

3 (25.0)

5 (13.9)

 SD

2 (16.7)

3 (25.0)

4 (33.3)

9 (25.0)

 PD

7 (58.3)

7 (58.3)

5 (41.7)

19 (52.8)

 Missing

2 (16.7)

1 (8.3)

0

3 (8.3)

ORR, n (%)

1 (8.3)

1 (8.3)

3 (25.0)

5 (13.9)

  95% CI

0.2-38.5

0.2-38.5

5.5-57.2

4.7-29.5

DCR, n (%)

3 (25.0)

4 (33.3)

7 (58.3)

14 (38.9)

  95% CI

5.5-57.2

9.9-65.1

27.7-84.8

23.1-56.5

PFS, months, median (95% CI)

1.8 (1.2-2.3)

1.7 (1.6-1.8)

3.5 (0.4-6.6)

1.8 (1.1-2.4)

OS, months, median (95% CI)

7.1 (0-14.6)

14.8 (3.5-26.1)

8.7 (4.3-13.1)

11.1 (6.8-15.4)

  1. PR Partial response, SD Stable disease, PD Progressive disease, ORR Objective response rate, DCR Disease control rate, PFS Progression-free survival, OS Overall survival, CI Confidence interval