Multivariate analysis of parameters predicting event-free survival and overall survival
Event-free survival . | RR . | 95% CI . | P . | Overall survival . | RR . | 95% CI . | P . |
---|---|---|---|---|---|---|---|
No Δ13 | 0.5 | 0.4-0.5 | <.0001 | No Δ13 | 0.4 | 0.4-0.6 | <.0001 |
B2M ≤2.5 mg/L | 0.7 | 0.6-0.8 | <.0001 | B2M ≤2.5 mg/L | 0.6 | 0.5-0.7 | <.0001 |
≤12 months SDT | 0.7 | 0.6-0.8 | <.0001 | ≤12 mo SDT | 0.7 | 0.6-0.9 | .0001 |
Sensitive to SDT | 0.8 | 0.7-0.9 | <.0001 | CRP ≤4.0 mg/L | 0.7 | 0.6-0.9 | <.0002 |
Any 2nd HDT* | 0.8 | 0.6-0.9 | .0004 | Sensitive to SDT | 0.8 | 0.6-0.9 | .0002 |
Non-IgA isotype | 0.7 | 0.6-0.9 | .002 | (Days to 2nd HDT)−1 * | 0.5 | 0.4-0.6 | .001 |
Any CR* | 0.8 | 0.6-0.9 | .002 | Any 2nd HDT* | 0.04 | 0.01-0.1 | <.0001 |
CRP ≤4.0 mg/L | 0.8 | 0.7-0.9 | .03 | Non-IgA isotype | 0.7 | 0.6-0.9 | .002 |
(Days to 2nd HDT)−1 * | .07 | Any CR* | 0.8 | 0.7-1.0 | .04 |
Event-free survival . | RR . | 95% CI . | P . | Overall survival . | RR . | 95% CI . | P . |
---|---|---|---|---|---|---|---|
No Δ13 | 0.5 | 0.4-0.5 | <.0001 | No Δ13 | 0.4 | 0.4-0.6 | <.0001 |
B2M ≤2.5 mg/L | 0.7 | 0.6-0.8 | <.0001 | B2M ≤2.5 mg/L | 0.6 | 0.5-0.7 | <.0001 |
≤12 months SDT | 0.7 | 0.6-0.8 | <.0001 | ≤12 mo SDT | 0.7 | 0.6-0.9 | .0001 |
Sensitive to SDT | 0.8 | 0.7-0.9 | <.0001 | CRP ≤4.0 mg/L | 0.7 | 0.6-0.9 | <.0002 |
Any 2nd HDT* | 0.8 | 0.6-0.9 | .0004 | Sensitive to SDT | 0.8 | 0.6-0.9 | .0002 |
Non-IgA isotype | 0.7 | 0.6-0.9 | .002 | (Days to 2nd HDT)−1 * | 0.5 | 0.4-0.6 | .001 |
Any CR* | 0.8 | 0.6-0.9 | .002 | Any 2nd HDT* | 0.04 | 0.01-0.1 | <.0001 |
CRP ≤4.0 mg/L | 0.8 | 0.7-0.9 | .03 | Non-IgA isotype | 0.7 | 0.6-0.9 | .002 |
(Days to 2nd HDT)−1 * | .07 | Any CR* | 0.8 | 0.7-1.0 | .04 |
Abbreviations: Δ13, chromosome 13 abnormalities; B2M, β-2-microglobulin; CR, complete remission; CRP, C-reactive protein; SDT, standard-dose therapy; HDT, high-dose therapy; RR, relative risk of experiencing event in favorable versus unfavorable categories; CI, confidence interval.
Time-dependent covariate.