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Table 1 Patient demographics and baseline disease characteristics

From: First-in-human, open-label dose-escalation and dose-expansion study of the safety, pharmacokinetics, and antitumor effects of an oral ALK inhibitor ASP3026 in patients with advanced solid tumors

Parameter/statistics

Dose-escalation cohort

Dose-expansion cohort (ALK-positive)

Both cohorts

Total (n = 30)a

525 mg (n = 16)b

All patients (n = 46)

Sex, n (%)

   

 Male

14 (47)

8 (50)

22 (48)

 Female

16 (53)

8 (50)

24 (52)

Race, n (%)

   

 White

25 (83)

1 (6)

26 (57)

 Black or African American

5 (17)

14 (88)

19 (41)

 Asian

0

1 (6)

1 (2)

Age (years)

   

 Mean (standard deviation)

61.6 (9.6)

51.1 (11.8)

57.9 (11.5)

 Median (range)

64 (44–77)

51 (19–71)

61 (19–77)

Weight (kg), mean (standard deviation)

80.3 (20.4)

75.0 (11.6)

78.5 (17.9)

ECOG performance status, n (%)

   

 Grade 0

6 (20)

9 (56)

15 (33)

 Grade 1

19 (63)

7 (44)

26 (57)

 Grade 2

5 (17)

0

5 (11)

Primary tumor type, n (%)

   

 Lung adenocarcinoma

4 (13)

7 (44)

11 (24)

 NSCLC

0

6 (38)

6 (13)

 Malignant lung neoplasm

0

2 (13)

2 (4)

 Breast

4 (13)

0

4 (9)

 Adenocarcinoma (unspecified primary)

3 (10)

0

3 (7)

 Leiomyosarcoma

3 (10)

0

3 (7)

 Colon

2 (7)

0

2 (4)

 Bile duct

2 (7)

0

2 (4)

 Ovarian

2 (7)

0

2 (4)

 Other

10 (33)

1 (6)

11 (24)

Brain metastases history, n (%)

9 (56)

Prior radiation therapy, n (%)

18 (60)

14 (88)

32 (70)

  1. ALK anaplastic lymphoma kinase, ECOG Eastern Cooperative Oncology Group, NSCLC non-small cell lung carcinoma, UNK unknown
  2. aExcludes 3 ALK-positive patients
  3. bIncludes 3 ALK-positive patients from the dose-escalation cohort