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Table 1 Baseline characteristics of patients

From: A phase I dose-escalation study of selumetinib in combination with docetaxel or dacarbazine in patients with advanced solid tumors

Characteristics, n (%)

Selumetinib + docetaxel (N = 35)

Selumetinib + dacarbazine (N = 25)

Age, years; mean (SD)

58.9 (9.5)

57.1 (11.5)

 Male

21 (60.0)

15 (60.0)

 Female

14 (40.0)

10 (40.0)

Race

 White

33 (94.3)

25 (100.0)

 Black/African American

2 (5.7)

0

WHO performance status

 0

14 (40.0)

12 (48.0)

 1

21 (60.0)

13 (52.0)

Primary tumor site

 Skin/soft tissue

11 (31.4)

17 (68.0)

 Lung

8 (22.9)

3 (12.0)

 Breast

3 (8.6)

0

 Colorectal

2 (5.7)

0

 Esophagus

2 (5.7)

0

 Ovary

2 (5.7)

0

 Head and neck

1 (2.9)

1 (4.0)

 Uveal

1 (2.9)

1 (4.0)

 Othera

5 (14.3)

3 (12.0)

Mean prior systemic treatments

3.1

2.0

Prior therapy, n (%)

 Chemotherapy

30 (85.7)

18 (72.0)

  Platinum compounds

24 (68.6)

9 (36.0)

  Taxanes

18 (51.4)

8 (32.0)

  Pyrimidine analogues

6 (17.1)

1 (4.0)

  Anthracyclines

5 (14.3)

3 (12.0)

 Radiotherapy

18 (51.4)

13 (52.0)

 Other systemic anticancer therapyb

8 (22.9)

8 (32.0)

 Immuno/hormonal therapy

6 (17.1)

0

 Hormonal therapy

3 (8.6)

0

 Immunotherapy

2 (5.7)

10 (40.0)

Prior lines of chemotherapy, n (%)

 0 or 1

17 (48.6)

21 (84.0)

 2 or 3

10 (28.6)

2 (8.0)

 4+

8 (22.9)

2 (8.0)

  1. aIncludes bladder, lymph nodes, melanoma, muscle, prostate, pancreas, stomach, unknown primary, and uterus
  2. bIncludes monoclonal antibodies, vaccines, small molecule targeted agents, and investigational drugs
  3. SD, standard deviation; WHO, World Health Organization