Skip to main content

Table 2 Summary of the antitumor effects

From: Efficacy of bevacizumab combined with erlotinib for advanced hepatocellular carcinoma: a single-arm meta-analysis based on prospective studies

Study

N

ORR

DCR

CR

PR

SD

PD

PFS (mon) Median (95% CI)

TTP (mon) (95%CI)

PFS-16w

OS (mon) Median (95% CI)

OS-12 m

OS-6 m

Grade3–4 AEs

Melanie 2018 [28]

90

15%

NA

NA

NA

NA

NA

4.37 (2.99–7.36)

NA

NA

8.6 (7.0–13.9)

37%

71.3%

19%

Kaseb 2016 [24]

44

9%

50%

0

9%

41%

9%

3.9 (2.0–8.3)

3.9 (2.0–8.3)

43%

9.9 (8.3–15.5)

NA

NA

NA

Govindarajan 2013 [21]

21

0

NA

NA

NA

NA

NA

2.57 (2.13–4.20)

2.57 (2.13–4.2)

28%(27w)

8.33 (5.73–13.97)

41.6%

68.7%

NA

Hsu 2013 [22]

51

6%

53%

NA

6%

47%

45%

2.9 (1.3–4.4)

2.9 (1.3–4.4)

35.3%

10.7 (6.2–15.2)

47.5%

69.1%

43.1%

Philip 2012 [25]

27

4%

52%

NA

4%

48%

48%;

3.0 (1.8–7.1)

3.0 (1.8–7.1)

NA

9.5 (7.1–17.1)

40.4%

74.4%

58%

Yau 2012 [27]

10

0

0

NA

0

0

0

1.51 (1.08–1.74)

1.81 (1.08–1.74)

NA

4.37 (1.08–11.66)

12.4%

38.1%

20%

Kaseb 2012 [23]

59

24%

80%

NA

24%

56%

10%

7.2 (5.6–8.3)

NA

64%

13.7 (9.6–19.7)

57.1%

83.6%

NA

Melanie 2009 [26]

40

25%

62.5%

NA

25%

37.5%

NR

9.0 (6.0–10.4)

NA

62.5%

15.7 (11–18)

63.1%

83.0%

22.5%

  1. Note: ORR objective response rate, DCR disease control rate, CR complete response rate, PR partial response rate, SD stable disease rate, PD progressive disease rate, PFS progression-free survival, OS overall survival, TTP median time to progression, AEs adverse effects, NA not available