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Table 4 Treatment exposure

From: Rucaparib in recurrent ovarian cancer: real-world experience from the rucaparib early access programme in Spain – A GEICO study

 

Maintenance (n = 18)

Treatment (n = 33)

Total (n = 51)

Initial dose 600 mg twice daily

18 (100%) ​

30 (91%) ​

48 (94%)

Treatment duration, months

7.5 (1.1–15.5) ​

2.4 (0.2–16.7) ​

3.3 (0.2–16.7) ​

Treatment duration*

0–12 months

12 (80%)

30 (97%)

42 (91%)

12–24 months

3 (20%)

1 (3%)

4 (9%)

Dose interruptions

10 (56%)

20 (63%)

30 (60%)

0

8 (44%)

12 (38%)

20 (40%)

1

8 (44%)

13 (41%)

21 (42%)

2

0

7 (22%)

7 (14%)

≥ 3

2 (11%)

0

2 (4%)

Dose reductions

11 (61%)

14 (44%)

25 (50%)

0

7 (39%)

18 (56%)

25 (50%)

1

5 (28%)

11 (34%)

16 (32%)

2

5 (28%)

3 (9.4)

8 (16%)

3

1 (6%)

0

1 (2%)

Reason for discontinuation

Progression

13 (72%)

25 (76%)

38 (75%)

Toxicity​

1 (6%)

4 (12%)

5 (10%)

Other

1 (6%)

2 (6%)

3 (6%)

On treatment

3 (17%)

2 (6%)

5 (10%)

  1. Data are median (range) or n (%). *Percentages calculated based on patients who had discontinued treatment. 1 patient in the treatment group was excluded from the analysis as the recommended dose modification scheme was not followed. Doctor’s or patient’s decision.