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Table 2 Response rates based on Intent-to-Treat population (n = 45) and in patients who have completed at least two cycles of the experimental combination (n = 42)

From: Phase II study of the combination carboplatin plus celecoxib in heavily pre-treated recurrent ovarian cancer patients

Characteristics

Intent-to-Treat patients

No (%)

Patients completing at least two cycles of treatment

No (%)

Patients

45

42

Clinical response

  

   Complete

3 (6.7)

3 (7.1)

   Partial

10 (22.2)

10 (23.8)

   Stable disease

13 (28.9)

12 (28.6)

   Progression

19 (42.2)

17 (40.5)

Duration of response, months

Median (range)

6 (3-13)

6 (3-13)

Duration of stabilization, months

Median (range)

5 (3-10)

5 (3-10)

Serological Response*

  

   Complete

8 (19.0)

8 (20.5)

   Partial

9 (21.4)

8 (20.5)

   Stabilization

12 (28.6)

11 (28.2)

   Progression

13 (31.0)

12 (30.8)

  1. *Patients with 2 pre-treatment samples above the upper limit of normal (35 U/ml) Ca125 levels, and at least 2 additional samples after the start of treatment (n = 42).