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Table 2 Objective response determined by RECIST v1.1

From: Bifunctional anti-PD-L1/TGF-βRII agent SHR-1701 in advanced solid tumors: a dose-escalation, dose-expansion, and clinical-expansion phase 1 trial

 

Gastric cancer (n=35)

Hepatocellular carcinoma (n=21)

Biliary tract cancer (n=13)

Urothelial carcinoma (n=12)

Head and neck squamous cell carcinoma (n=10)

Renal cell carcinoma (n=10)

Pancreatic cancer (n=10)

Esophageal cancer (n=10)

Best overall response

 Complete response

1 (3%)

0

0

1 (8 %)

0

0

0

0

 Partial response

6 (17 %)

1 (5%)

1 (8%)

1 (8%)

2 (20%)

2 (20%)

0

0

 Stable disease

6 (17%)

6 (29%)

1 (8%)

1 (8%)

4 (40%)

1 (10%)

2 (20%)

3 (30%)

 Progressive disease

19 (54%)

11 (52%)

9 (69%)

6 (50%)

2 (20%)

5 (50%)

8 (80%)

4 (40%)

 Not evaluable

3 (9%)

3 (14%)

2 (15%)

3 (25%)

2 (20%)

2 (20%)

0

3 (30%)

Objective response rate

20.0% (8.4–36.9)

4.8% (0.1–23.8)

7.7% (0.2–36.0)

16.7% (2.1–48.4)

20.0% (2.5–55.6)

20.0% (2.5–55.6)

0% (0–30.9)

0% (0–30.9)

Disease control rate

37.1% (21.5–55.1)

33.3% (14.6–57.0)

15.4% (1.9–45.5)

25.0% (5.5–57.2)

60.0% (26.2–87.8)

30.0% (6.7–65.3)

20.0% (2.5–55.6)

30.0% (6.7–65.3)

Clinical benefit rate

28.6% (14.6–46.3)

9.5% (1.2–30.4)

7.7% (0.2–36.0)

16.7% (2.1–48.4)

30.0% (6.7–65.3)

30.0% (6.7–65.3)

0% (0–30.9)

10.0% (0.3–44.5)

  1. Data are n (%) or % (95% CI)