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Table 4 Tumor responses assessed by investigator

From: First-in-human phase I study of BPI-9016M, a dual MET/Axl inhibitor, in patients with non-small cell lung cancer

 

Group

 

1 0 mg/qd

200 mg/qd

300 mg/qd

450 mg/qd

600 mg/qd

800 mg/qd

Total

(n = 4)

(n = 3)

(n = 3)

(n = 4)

(n = 3)

(n = 3)

(N = 20)

Partial remission (PR)

0

0

0

0

0

1 (33.3%)

1 (5.3%)

Stable disease (SD)

0

2 (66.7%)

2 (66.7%)

2 (50.0%)

2 (66.7%)

2 (66.7%)

10 (52.6%)

Progressive disease (PD)

3 (100.0%)

1 (33.3%)

1 (33.3%)

2 (50.0%)

1 (33.3%)

0

8 (42.1%)

Total

3 (100.0%)

3 (100.0%)

3 (100.0%)

4 (100.0%)

3 (100.0%)

3 (100.0%)

19 (100.0%)

Missing

1

0

0

0

0

0

1

Objective remission rate, %

(95%CI)

0 (NA, NA)

0 (NA, NA)

0 (NA, NA)

0 (NA, NA)

0 (NA, NA)

33.3 (0.84, 90.57)

5.3 (0.13, 26.03)

Disease control rate, %

(95%CI)

0 (NA, NA)

66.7 (9.43, 99.16)

66.7 (9.43, 99.16)

50.0 (6.76, 93.24)

66.7 (9.43, 99.16)

100.0(29.24,100.0)

57.9 (33.50, 79.75)

  1. The objective remission rate (ORR) and disease control rate (DCR) were calculated based on the overall assessment. The ORR was calculated as the proportion of patients who achieved complete remission (CR) and partial remission (PR). The DCR was calculated as the proportion of patients who achieved CR, PR, and stable disease (SD). Overall evaluation did not require confirmation of the efficacy of CR or PR and was the best response at all points in the trial