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. 2020 Jul 20;35(3):809–822. doi: 10.1038/s41375-020-0976-9

Table 5.

Multivariate models on time-to-progression and non-relapse mortality from randomization.

Factor TTP NRM
HR (95% CI) p HR (95% CI) p
Age group S2 (vs. S1) 1.19 (0.86–1.63) 0.29 2.20 (0.95–5.08) 0.06
Age group S3 (vs. S1) 0.94 (0.70–1.25) 0.65 1.67 (0.74–3.76) 0.21
Induction therapy (VCD) 0.87 (0.68–1.10) 0.25
Maintenance strategy (LEN-CR) 1.15 (0.90–1.45) 0.26
Sex (male) 1.32 (1.03–1.69) 0.03
ISS stage II 1.50 (1.12–2.00) 0.006
ISS stage III 1.71 (1.25–2.34) <0.001
LDH (>ULN) 1.51 (1.08–2.11) 0.02
Adverse cytogenetics (yes) 1.91 (1.48–2.46) <0.001
IgA subtype (yes) 1.06 (0.80–1.41) 0.69
WHO PS (>1) 1.17 (0.78–1.74) 0.45 3.49 (1.56–7.80) 0.002
Cardiac/vascular disorders (>1) 0.75 (0.28–1.97) 0.56

Age groups are defined as: ≤60 years (S1), 61–65 years (S2) and 66–70 years (S3). Adverse cytogenetics were defined as at least one of the following aberrations: deletion17p13, translocation t(4;14), translocation t(14;16), gain 1q21 (>3 copies).

Bold p values are statistically significant.

VCD bortezomib, cyclophosphamide, dexamethasone, LEN lenalidomide, CR complete response, WHO World Health Organization, PS performance status, ISS International Staging System, LDH lactate dehydrogenase, ULN upper limit of normal, Ig immunoglobulin.