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Table 1 Patients baseline demographics and disease characteristics

From: Selinexor in combination with standard chemotherapy in patients with advanced or metastatic solid tumors

Characteristic

Selinexor 60 mg QW/BIW  +  carboplatin 6 AUC Q3W (N  = 6)

Selinexor 60 mg QW/BIW  +  doxorubicin 60 mg/m2  +  cyclophosphamide 600 mg/m2 Q3W (N  = 4)

Selinexor 40 mg QW  +  FOLFIRIa (N  = 3)

Selinexor 60 mg QW  + irinotecan 125 mg/m2 D1 and 8 Q3W (N  = 3)

Selinexor 40 mg QW  +  XELOXb (N  = 3)

All patients (N  = 19)

Age at consent (years)

 Median range

56.1 (31.2–76.1)

61.7 (23.6–64.9)

49.9 (38.1–70.7)

67.8 (57.9–72.3)

65.9 (51.8–72.8)

60.6 (23.6–76.1)

Gender, N (%)

 Male

1 (17)

2 (50)

1 (33)

1 (33)

2 (67)

7 (37)

 Female

5 (83)

2 (50)

2 (67)

2 (67)

1 (33)

12 (63)

Race/ethnicity, N (%)

 White

4 (67)

4 (100)

3 (100)

1 (33)

3 (100)

15 (79)

 Hispanic

0

0

0

0

0

0

 Black

1 (17)

0

0

1 (33)

0

2 (11)

 Asian

1 (17)

0

0

1 (33)

0

2 (11)

ECOG performance status, N (%)

 0

1 (17)

0

1 (33)

2 (67)

1 (33)

5 (26)

 1

5 (83)

4 (100)

2 (67)

1 (33)

2 (67)

14 (74)

Primary tumor, N (%)

 Ovarian

0

2 (50)

0

0

0

2 (11)

 Breast

3 (50)

0

0

0

0

3 (16)

 Colorectal cancer

0

0

1 (33)

1 (33)

1 (33)

3 (16)

 Endometrial/fallopian

0

0

0

0

0

0

 Lung

1 (17)

0

0

0

0

1 (5)

 Neuroendocrine

0

0

1 (33)

1 (33)

0

2 (11)

 Pancreas

0

0

1 (33)

0

1 (33)

2 (11)

 Esophageal

0

0

0

0

0

0

 Head and neck/salivary gland

1 (17)

0

0

1 (33)

0

2 (11)

 Liver/cholangiocarcinoma

0

0

0

0

1 (33)

1 (5)

 Sarcoma

0

1 (25)

0

0

0

1 (5)

 Prostate

0

1 (25)

0

0

0

1 (5)

 Others

1 (17)

0

0

0

0

1 (5)

Prior lines of systemic therapies, N (%)

 0–1

1 (17)

0

0

0

0

1 (5)

 2–3

4 (67)

3 (75)

2 (67)

2 (67)

2 (67)

13 (68)

 4–5

1 (17)

1 (25)

1 (33)

0

1 (33)

4 (21)

 > 5

0

0

0

1 (33)

0

1 (5)

 Median range

2.5 (1.0–4.0)

2.0 (2.0–4.0)

3.0 (3.0–5.0)

3.0 (2.0–6.0)

3.0 (2.0–4.0)

3.0 (1.0–6.0)

  1. N number; ECOG Eastern Cooperative Oncology Group; QW once weekly; BIW twice weekly; AUC area under curve; mg/m2 milligrams per square meter; D1 and 8 on days 1, and 8 of each cycle; Q3W every 3 week; FOLFIRI irinotecan with fluorouracil and folinic acid; XELOX capecitabine and oxaliplatin
  2. aFOLFIRI—irinotecan of 180 mg/m2, 5-FU continuous infusion of 2400 mg/m2, 5-FU bolus of 400 mg/m2, and leucovorin of 400 mg/m2 on days 1, and 15
  3. bXELOX—capecitabine was dosed at 900 mg/m2 orally (PO) divided into 2 doses on days 1–14, along with oxaliplatin of 130 mg/m2 IV Q3W