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. 2020 Jun 10;37(7):3404–3416. doi: 10.1007/s12325-020-01395-x

Table 1.

Baseline demographics and disease characteristics of Asian subgroups

Denosumab 120 mg SC Q4W (N = 103)a Zoledronic acid 4 mg IV Q4W (N = 93)b
Sex, n (%)
 Men 65 (63.1) 43 (46.2)
 Women 38 (36.9) 50 (53.8)
Age, median (Q1, Q3) 61.0 (54.0, 69.0) 61.0 (54.0, 68.0)
ECOG performance status at study entry, n (%)
 0 33 (32.0) 24 (25.8)
 1 45 (43.7) 52 (55.9)
 2 25 (24.3) 17 (18.3)
Multiple myeloma ISS stage at diagnosis, n (%)
 I 25 (24.3) 31 (33.3)
 II 35 (34.0) 36 (38.7)
 III 42 (40.8) 26 (28.0)
 Not available 1 (1.0) 0
History of SREs, n (%)
 Any SRE 64 (62.1) 70 (75.3)
  Pathological fracture 57 (55.3) 60 (64.5)
  Spinal cord compression 14 (13.6) 16 (17.2)
  Radiation therapy to bone 6 (5.8) 8 (8.6)
  Surgery to bone 9 (8.7) 22 (23.7)
Prior radiotherapy to soft tissue/mass for multiple myeloma, n (%) 2 (1.9) 6 (6.5)
Prior oral bisphosphonate use, n (%) 1 (1.0) 4 (4.3)
Class of the first-line therapy, n (%)
 PI only 37 (35.9) 42 (45.2)
 IMiD only 26 (25.2) 31 (33.3)
 PI + IMiD 32 (31.1) 17 (18.3)
 Other 7 (6.8) 3 (3.2)
Cytogenetics risk group, n (%)
 Standard risk 77 (74.8) 71 (76.3)
 High risk 10 (9.7) 9 (9.7)
 Unknown 16 (15.5) 13 (14.0)

ECOG Eastern Cooperative Oncology Group, IMiD immunomodulatory drug, ISS International Staging System, IV intravenously, PI proteasome inhibitor, Q4W every 4 weeks, SC subcutaneously, SRE skeletal-related event

aOf the 103 patients randomized to denosumab, 36 (35%) were from Korea, 24 (23%) were from Japan, 15 (15%) were from Taiwan, 15 (15%) were from Singapore, 8 (8%) were from Malaysia, and 5 (5%) were from Hong Kong

bOf the 93 patients randomized to zoledronic acid, 48 (52%) were from Korea, 18 (19%) were from Japan, 11 (12%) were from Taiwan, 6 (6%) were from Singapore, 6 (6%) were from Malaysia, and 4 (4%) were from Hong Kong