Skip to main content

Table 1 Patient baseline characteristics

From: A multicenter phase 2 study of pomalidomide plus dexamethasone in patients with relapsed and refractory multiple myeloma: the Japanese MM-011 trial

Characteristic

Pomalidomide plus dexamethasone (N = 36)

Age

 Median (range), years

64.5 (43–78)

 >65 years, n (%)

17 (47.2)

 >75 years, n (%)

4 (11.1)

Sex, n (%)

 Male

16 (44.4)

 Female

20 (55.6)

Time from first diagnosis, median (range), years

4.7 (0.6–21.1)

ECOG performance status, n (%)

 0–1

33 (91.7)

 2

3 (8.3)

Durie–Salmon stage, n (%)

 I

7 (19.4)

 II

16 (44.4)

 III

13 (36.1)

β2-microglobulin level, n (%)

 <3.5 mg/L

24 (66.7)

 3.5–<5.5 mg/L

10 (27.8)

 ≥5.5 mg/L

2 (5.6)

Bone lesions, n (%)

22 (61.1)

Extramedullary plasmacytoma, n (%)

5 (13.9)

Creatinine clearance, n (%)

 <30 mL/min

0

 30–<45 mL/min

0

 45–<60 mL/min

8 (22.2)

 60–<80 mL/min

13 (36.1)

 ≥80 mL/min

15 (41.7)

Prior antimyeloma therapies, median (range)

6.5 (2–15)

Prior stem cell transplant, n (%)

19 (52.8)

Prior therapies, n (%)

 Lenalidomide

36 (100.0)

 Bortezomib

36 (100.0)

 Thalidomide

12 (33.3)

 Dexamethasone

35 (97.2)

 Melphalan

31 (86.1)

Last prior therapy, n (%)

 Lenalidomide

21 (58.3)

 Bortezomib

15 (41.7)

Refractory to prior therapies, n (%)

 Lenalidomide

35 (97.2)

 Bortezomib

21 (58.3)

 Both lenalidomide and bortezomib

21 (58.3)

  1. ECOG Eastern Cooperative Oncology Group