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Table 1 Patient characteristics

From: Transcriptional changes induced by bevacizumab combination therapy in responding and non-responding recurrent glioblastoma patients

 

All patients (n = 21)

Responders (n = 7)

Non-responders (n = 14)

P- value

Gender, n (%)

 Male

11 (52)

5 (71)

6 (43)

0.36

 Female

10 (48)

2 (29)

8 (57)

 

Age, years (range)

 Median

52 (21–70)

53 (35–65)

48 (21–70)

0.66

WHO performance status, n (%)

 0

10 (48)

2 (29)

8 (57)

0.42

 1

9 (43)

4 (57)

5 (36)

 

 2

2 (9)

1 (14)

1 (7)

Secondary glioblastoma, n (%)

 Yes

1 (5)

0

1 (7)

1.00

 No

20 (95)

7 (100)

13 (93)

 

Standard glioblastoma therapy, n (%)

 Yes

20 (95)

7 (100)

13 (93)

1.00

 No

1 (5)

0

1 (7)

 

Prior lines of chemotherapy, n (%)

 1

18 (86)

7 (100)

11 (79)

0.52

 2

3 (14)

0

3 (21)

 

Tumor size, cm2 (range)

 Median

9 (1–28)

11 (4–28)

8 (1–16)

0.65

Multifocal disease, n (%)

 Yes

2 (10)

0

2 (14)

0.53

 No

19 (91)

7 (100)

12 (86)

 

Corticosteroid use, n (%)a

 Yes

14 (67)

3 (43)

11 (79)

0.16

 No

7 (33)

4 (57)

3 (21)

 

Neurocognitive deficit, n (%)

 Yes

8 (38)

3 (43)

4 (29)

0.35

 No

13 (62)

4 (57)

10 (71)

 

Primary sample, before bevacizumab, n (%)

 Initial glioblastoma diagnosis

10 (48)

3 (43)

7 (50)

1.00

 Relapse surgery prior to bevacizumab

11 (52)

4 (57)

7 (50)

 

Time duration from relapse surgery (after bevacizumab), months

 to initiation of standard therapy, median

17

17

17

0.76

 to last bevacizumab administration, median

2

2

2

0.26

Number of bevacizumab treatment cyclesb

 Median

6

8

6

0.08

Bevacizumab combination therapy, n (%)

 Irinotecan

17 (81)

6 (86)

11 (79)

1.00

 Irinotecan and cetuximab

4 (19)

1 (14)

3 (21)

 

Response, n (%)

 Response (CR + PR)

7 (33)

7 (100)

0

 

 Stable disease

10 (48)

0

10 (71)

 Progressive disease

4 (19)

0

4 (29)

Progression-free survival, months

  Median

5.4

10.8

3.9

0.02

Overall survival, months

  Median

10.8

14.3

8.6

0.16

  1. Abbreviations: CR complete response, PR partial response
  2. a Prednisolone >10 mg
  3. b Two bevacizumab combination treatments (28 days) defined one treatment cycle