Table 1 Patient characteristics.

From: Randomized phase II trial of weekly ixabepilone ± biweekly bevacizumab for platinum-resistant or refractory ovarian/fallopian tube/primary peritoneal cancer (NCT03093155): Updated survival and subgroup analyses

 

IXA (n = 37)

IXA+BEV (n = 39)

Age in years, median (range)

67 (50–88)

67 (40–78)

Race, % (N)

  White

73% (27)

80% (31)

  Black

22% (8)

10% (4)

  Other

5% (2)

10%(4)

Ethnicity, % (N)

  Hispanic

8% (3)

3% (1)

  Non-Hispanic

92% (34)

95% (37)

  Unknown

0

3% (1)

Histology, % (N)

  Serous

78% (29)

87% (34)

  Carcinosarcoma

6% (2)

3% (1)

  Other

16% (6)

10% (4)

ECOG Performance Status, % (N)

  0–1

84% (31)

92% (36)

  2

16% (6)

8 % (3)

Prior Lines of Chemotherapy, % (N)

  ≤3

49% (18)

54% (21)

  >3

51% (19)

46% (18)

Prior PARP Inhibitor

  Yes

38% (14)

26% (10)

  No

62% (23)

74% (29)

Prior Bevacizumab, % (N)

  Yes

57% (21)

54% (21)

  No

43% (16)

46% (18)

Prior Weekly Paclitaxel (for first line treatment or treatment of recurrence), % (N)

  Yes

35% (13)

26% (10)

  No

65% (24)

74% (29)

Prior Receipt of an AURELIA Regimen, % (N)

  - With Bevacizumab

   Weekly paclitaxel

29% (2)

33% (2)

   Pegylated liposomal doxorubicin

29% (2)

66% (4)

   Topotecan

14% (1)

0

  > 1 AURELIA regimen

29% (2)

0

- Without Bevacizumab

  Weekly paclitaxel

17% (2)

11% (2)

  Pegylated liposomal doxorubicin

58% (7)

67% (12)

  Topotecan

8% (1)

17% (3)

  >1 AURELIA regimen

17% (2)

5% (1)

Platinum Refractory/Resistant Disease, % (N)

  Refractory

11% (4)

26% (10)

  Resistant

89% (33)

74% (29)

Taxane Refractory/Resistant Disease, % (N)

  Refractory

27% (10)

33% (13)

  Resistant

24% (9)

33% (13)

  Sensitive

49% (18)

33% (13)

  1. ECOG Eastern Cooperative Oncology Group