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Table 1 Patients’ demographics

From: Safety and efficacy of afatinib as add-on to standard therapy of gemcitabine/cisplatin in chemotherapy-naive patients with advanced biliary tract cancer: an open-label, phase I trial with an extensive biomarker program

Variable

Dose level 1

(N = 3)

Dose level − 1

(N = 6)

Total

(N = 9)

Age [Years]

 N

3

6

9

 Mean (SD)

62.00 (21.63)

60.17 (7.31)

60.78 (12.30)

 Min

38.0

51.0

38.0

 Median

68.00

59.00

60.00

 Max

80.0

71.0

80.0

 Missing

0

0

0

Gender

 Female

1 (33.33%)

3 (50.00%)

4 (44.44%)

 Male

2 (66.67%)

3 (50.00%)

5 (55.56%)

Ethnicity

 Caucasian

3 (100.00%)

6 (100.00%)

9 (100.00%)

Primary tumour

 Intrahepathic tumour

3 (100.00%)

3 (50.00%)

6 (66.67%)

 Extrahepatic tumour

0 (0.00%)

3 (50.00%)

3 (33.33%)

ECOG

 0

2 (66.67%)

2 (33.33%)

4 (44.44%)

 1

1 (33.33%)

4 (66.67%)

5 (55.56%)

Metastatic disease

3 (100.00%)

6 (100.00%)

9 (100.00%)

Target lesions

 Primary tumour

1 (14.29%)

1 (10.00%)

2 (11.76%)

 Liver

3 (42.86%)

3 (30.00%)

6 (35.29%)

 Lung

2 (28.57%)

2 (20.00%)

4 (23.53%)

 Other lymph nodes

1 (14.29%)

0 (0.00%)

1 (5.88%)

 Peritoneum

0 (0.00%)

1 (10.00%)

1 (5.88%)

 Soft tissues

0 (0.00%)

1 (10.00%)

1 (5.88%)

 Others

0 (0.00%)

2 (20.00%)

2 (11.76%)

  1. SD Standard Deviation