Table 1 Demographics and baseline characteristics (safety population)

From: Safety, pharmacokinetics, and preliminary efficacy of E6201 in patients with advanced solid tumours, including melanoma: results of a phase 1 study

 

Part A (n = 25)

Part B (n = 30)

Median age (range), years

66 (44–87)

56 (28–79)

Gender, n (%)

 Male

10 (40.0)

15 (50.0)

 Female

15 (60.0)

15 (50.0)

ECOG performance status, n (%)

 0

14 (56.0)

9 (30.0)

 1

11 (44.0)

21 (70.0)

Tumour type, n (%)

  

 Melanoma

3 (12.0)

30 (100)

 Colon

5 (20.0)

0

 Breast

2 (8.0)

0

 Prostate

2 (8.0)

0

 Gall bladder

2 (8.0)

0

 Pancreas

2 (8.0)

0

 Papillary thyroid

2 (8.0)

0

 Othera

7 (28.0)

0

Tumour mutational status, n (%)

 BRAF-mutated/BRAF-WT

3 (12.0)/15 (60.0)b

23 (76.7)/7 (23.3)

 KRAS-mutated/KRAS-WT

3 (12.0)/15 (60.0)b

Not collected in Part B

Number of previous therapies for locally advanced or metastatic disease, n (%)

 0

3 (12.0)

7 (23.3)

 1

3 (12.0)

12 (40.0)

 2

7 (28.0)

7 (23.3)

 3

6 (24.0)

2 (6.7)

 4

3 (12.0)

2 (6.7)

 ≥5

3 (12.0)

0

Type of prior therapy, n (%)

 Radiotherapy

10 (40.0)

15 (50.0)

 Neoadjuvant

2 (8.0)

0

 Adjuvant

8 (32.0)

8 (26.7)

  1. aDuodenal, GIST, rectal, GE junction, hepatobiliary, thyroid, gastric carcinoid (n = 1 each).
  2. bMutation status based on archival tumour tissue, no sample/status unknown for 7 patients.
  3. GE gastroesophageal, GIST gastrointestinal stromal tumour, WT wildtype