Table 3.
Univariate analysis | Multivariate analysis | |||
---|---|---|---|---|
Time to mCRPC | Hazard ratio (95% CI) | p value | Hazard ratio (95% CI) | p value |
Model 1 | ||||
Any gDDRm | 2.37 (1.48–3.80) | <.001 | 1.98 (1.22–3.23) | .006 |
Treatment (combination therapy vs. ADT alone) | 1.00 (0.62–1.63) | .9 | 0.86 (0.51–1.43) | .6 |
Age of onset, yr | 0.99 (0.96–1.01) | .4 | 0.99 (0.97–1.02) | .5 |
Baseline PSA (log), ng/mL | 1.38 (0.99–1.91) | .058 | 1.14 (0.79–1.64) | .5 |
Gleason grade group (4–5 vs. 1–3) | 1.63 (0.84–3.16) | .15 | 1.85 (0.95–3.61) | .070 |
High‐volume disease (present vs. absent) | 1.86 (1.17–2.94) | .008 | 1.74 (1.07–2.82) | .024 |
PSA nadir within the first 7 mo (>4 vs. ≤4), ng/mL | 1.36 (0.91–2.04) | .13 | 1.57 (1.02–2.41) | .042 |
Model 2 | ||||
mBRCA2 mutation | 3.73 (2.12–6.58) | <.001 | 3.14 (1.76–5.60) | <.001 |
Treatment (combination therapy vs. ADT alone) | 0.94 (0.57–1.55) | .8 | 0.67 (0.39–1.14) | .14 |
Age of onset, yr | 0.99 (0.97–1.01) | .4 | 0.99 (0.97–1.02) | .8 |
Baseline PSA (log), ng/mL | 1.32 (0.94–1.86) | .11 | 1.05 (0.72–1.53) | .8 |
Gleason grade group (4–5 vs. 1–3) | 1.48 (0.74–2.98) | .3 | 1.25 (0.61–2.55) | .5 |
High‐volume disease (present vs absent) | 1.93 (1.20–3.11) | .007 | 1.97 (1.21–3.22) | .007 |
PSA nadir within the first 7 mo (>4 vs ≤4), ng/mL | 1.42 (0.93–2.16) | .10 | 1.55 (0.98–2.44) | .059 |
Model 1 evaluated the effect of any gDDRm versus wild‐type. Model 2 evaluated the effect of BRCA2 mutation versus wild‐type.
High‐volume disease was defined as the presence of visceral metastases or ≥ 4 bone lesions with at least one outside of the vertebral column and pelvis according to the CHAARTED trial.
Abbreviations: ADT, androgen deprivation therapy; CI, confidence interval; gDDRm, germline DNA repair gene mutations; PSA, prostate‐specific antigen.