Table 6 Objective response rates

From: A phase I/II trial of irinotecan–cisplatin combined with an anti-late-diarrhoeal programme to evaluate the safety and antitumour response of this combination therapy in patients with advanced non-small-cell lung cancer

  

CR

PR

CR+PR

PD

Group

No. of evaluable patients

No.

No.

No.

%

No.

%

Phase I

60N

7

0

1

1

14.3

2

28.6

60P

5

0

1

1

20.0

2

40.0

65P

4

0

3

3

75.0

0

0

70P

3

0

0

0

0

1

33.3

75P

6

1

3

4

66.0

0

0

80P

2

0

1

1

50

0

0

Phase II

48

0

30

30

62.5 (47.3–76.0)a

7

14.6 (6.1–27.8)

Total

75

1

39

40

53.3 (41.4–64.9)

12

16.0 (8.5–26.3)

  1. CR, complete response; PR, partial response; PD, progressive disease defined by WHO response criteria.
  2. a95% confidential interval.