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Table 1 Baseline demographics and disease characteristics

From: Selinexor plus low-dose dexamethasone in Chinese patients with relapsed/refractory multiple myeloma previously treated with an immunomodulatory agent and a proteasome inhibitor (MARCH): a phase II, single-arm study

Baseline characteristics

mITT population (N = 82)

Median age, years (range)

60.0 (42, 82)

Patient age, n (%)

 ≥65

32 (39.0)

Gender, n (%)

 Male

43 (52.4)

 Female

39 (47.6)

Baseline ECOG performance status, n (%)

 0

26 (31.7)

 1

54 (65.9)

 2

2 (2.4)

Tumor burden increase (screening to pre-dose), n (%)

60 (73.2)

 Median, %

23.1

 Range, %

2.1–317.9

MM subtype at baseline, n (%)

 IgG

40 (48.8)

 IgA

17 (20.7)

 IgD

7 (8.5)

 Others

19 (23.2)

R-ISS stage at baseline, n (%)

 I

23 (28.0)

 II

50 (61.0)

 III

9 (11.0)

High-risk cytogenetic abnormalities

55 (67.1)

 del 17p13

18 (22.0)

 t(4;14)

21 (25.6)

 t(14;16)

5 (6.1)

 1q amplification

53 (64.6)

Creatinine clearance, mL/min, n (%)

 <30

3 (3.7)

 30–<60

15 (18.3)

 ≥60

64 (78.0)

Median time since initial MM diagnosis, years (range)

3.2 (0.2–13.4)

Respond to last regimen (≥PR), n (%)

24 (29.3)

Median prior regimens (range)

5 (1–16)

Prior therapy, n (%)

 Lenalidomide

  Exposed vs refractory

82 (100.0) vs 82 (100.0)

 Bortezomib

  Exposed vs refractory

82 (100.0) vs 82 (100.0)

 Daratumumab

  Exposed vs refractory

23 (28.0) vs 20 (24.4)

 Ixazomib

  Exposed vs refractory

28 (34.1) vs 26 (31.7)

 Carfilzomib

  Exposed vs refractory

6 (7.3) vs 5 (6.1)

 Pomalidomide

  Exposed vs refractory

10 (12.2) vs 9 (11.0)

 Prior ASCT

18 (22.0)

 Prior CAR-T

10 (12.2)

  1. ASCT Autologous stem cell transplantation, CAR Chimeric antigen receptor, ECOG Eastern Cooperative Oncology Group, mITT Modified intent-to-treat, MM Multiple myeloma, R-ISS Revised-International Staging System