Table 1 Demographics and baseline disease characteristicsa.

From: Ofatumumab maintenance prolongs progression-free survival in relapsed chronic lymphocytic leukemia: final analysis of the PROLONG study

 

Ofatumumab (n = 240)

Observation (n = 240)

Age, yearsb

 Median (min–max)

64.0 (33–86)

64.5 (39–87)

 <70, n (%)

167 (70)

166 (69)

 ≥70, n (%)

73 (30)

74 (31)

 ≥75, n (%)

42 (18)

35 (15)

Sex, n (%)

 Female

79 (33)

80 (33)

 Male

161 (67)

160 (67)

Time since diagnosis, median (range) in year

6.0 (1–22)

5.0 (1–22)

Response to last CLL treatment, n (%)

 CR

47 (20)

47 (20)

 PR

193 (80)

192 (80)

 Missing

0

1 (<1)

Baseline MRD, n (%)

 Negative

31 (13)

42 (18)

 Positive

139 (58)

107 (45)

 Missing

70 (29)

91 (38)

No. of prior treatments, n (%)

 2

169 (70)

168 (70)

 3

67 (28)

63 (26)

 Other

4 (2)

9 (4)

Type of last prior treatment, n (%)

 Chemoimmunotherapy

193 (80)

193 (80)

 BR

46 (24)

48 (25)

 FCR

100 (52)

105 (54)

 FR

4 (2)

5 (3)

 Other

30 (16)

24 (12)

 RCVP

13 (7)

11 (6)

 Alkylating monotherapy

14 (6)

9 (4)

 Other

33 (14)

38 (16)

Baseline cytogenetics, n (%)c

 11q deletion

15 (6)

13 (5)

 17p deletion

7 (3)

4 (2)

 6q deletion or 12q trisomy or 13q deletion

47 (20)

16 (7)

 No aberration

151 (63)

174 (73)

 Missing

20 (8)

33 (14)

IGVH mutational status, n (%)

 Mutated

54 (23)

74 (31)

 Unmutated

139 (58)

116 (48)

 Not available

3 (1)

1 (<1)

 Missing

44 (18)

49 (20)

  1. BR bendamustine and rituximab, CLL chronic lymphocytic leukemia, CR complete remission, FCR fludarabine, cyclophosphamide, and rituximab, FR fludarabine and rituximab, IGVH immunoglobulin variable heavy-chain gene, ITT intent-to-treat, MRD minimal residual disease, PR partial remission, RCVP rituximab, cyclophosphamide, vincristine, and prednisone
  2. aITT population
  3. bAge was calculated from birth date to screening date in years
  4. c12% cutoff