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Table 1 Efficacy outcomes with antiangiogenic agents in recurrent glioblastoma.

From: Antiangiogenic agents in the treatment of recurrent or newly diagnosed glioblastoma: Analysis of single-agent and combined modality approaches

Reference, (na)

Treatment regimen

Response rate (%)b

Progression-free survival

  

CR

PR

SD

Median

At 6 months (%)

Bevacizumab

      

Vredenburgh [28], (n = 23 of 32)d

BV + irinotecan

4

57

35

20 weeks

30

Vredenburgh [29], (N = 35)

BV + irinotecan

57

N/A

24 weeks

46

Narayana [33], (n = 37 of 61)e

BV + irinotecan or carboplatin

13

60

21

5 months

N/A

Friedman [31], Cloughesy [32], (N = 167)

BV alone (n = 85)

BV + irinotecan (n = 82)

28

38

N/A

N/A

4.2 months

5.6 months

43

50

Reardon [38], (n = 27 of 59)d

BV + etoposide

4

19

70

18 weeks

44

Kreisl [49], (N = 48)

BV → BV + irinotecan

71 (Levin criteria); 35 (MacDonald criteria)

N/A

16 weeks

29

Gutin [92], (n = 20 of 25)d

BV + hypofractionated stereotactic irradiation

50

N/A

7.3 months

65

Aflibercept

      

De Groot [53], (n = 32 of 48)d

Aflibercept alone

0

30

52

N/A

N/A

Cediranib

      

Batchelor [112], (N = 31)

Cediranib alone

57 (volumetric criteria); 27 (MacDonald criteria)

N/A

117 days

26

Cilengitide

      

Reardon [50] (N = 81)

Cilengitide alone (2000 mg/d [n = 40] or 500 mg/d [n = 41])

0

9

N/A

2000 mg/d, 8.1 weeksc

500 mg/d, 7.9 weeksc

2000 mg/d, 15

500 mg/d, 10

CT-322

      

Schiff [113], (n = 51)

CT-322 alone (n = 33)

CT-322 + irinotecan (n = 18)

1 (3)

0

1 (3)

0

N/A

N/A

N/A

N/A

23

48

XL184

      

Wen [54], (n = 105)

XL184 175 mg qd

XL 184 125 mg qd

AAT-naive (n = 34), 21

AAT-pretreated (n = 12), 8

AAT-naive (n = 37), 30

AAT-pretreated (n = 22), 0

N/A

AAT-naive, 16 weeks

AAT-naive, 16 weeks

AAT-pretreated, 7.9 weeks

AAT-naive, 10

AAT-naive, 25

AAT-pretreated, 0

  1. Abbreviations: AAT = antiangiogenic therapy; BV = bevacizumab; CR = complete response; N/A = not available; PR = partial response; RT = radiotherapy; SD = stable disease.
  2. aNumber of patients with glioblastoma, where available.
  3. bIn evaluable patients.
  4. cTime to progression.
  5. dEfficacy outcomes are reported for patients with glioblastoma only.
  6. eEfficacy outcomes are reported for all patients.