Table 2. Relationship between clinical parameters and clinical outcome measures.
Time to biochemical relapse | Survival from biochemical relapse | Disease-specific survival | |
---|---|---|---|
Age (<70 vs ⩾70 years) | 0.260 | 0.385 | 0.020 |
Gleason (<7 vs =7 vs >7) | 0.013 | 0.754 | 0.008 |
Diagnosis PSA (<10 vs 10–20 vs >20 ng ml−1) | 0.002 | 0.078 | 0.001 |
Recurrence PSA (<10 vs 10–20 vs >20 ng ml−1) | <0.001 | <0.001 | |
Lymphovascular invasion (presence vs absence) | 0.001 | 0.612 | 0.114 |
Presence of metastases (presence vs absence) | 0.001 | 0.008 | <0.001 |
Ki67 (⩽median vs >median) | 0.730 | 0.279 | 0.033 |
Abbreviation: PSA=prostate specific antigen.
The clinical variables were grouped and analysed by Kaplan–Meier methods with reference to clinical outcome measures as shown. Patients were considered to have biochemical relapse dependent on treatment; radical prostatectomy serum PSA >0.2 ng ml−1, radical radiotherapy serum PSA of 2.0 ng ml−1 above the post-treatment nadir level, hormone treatment 2–3 consecutive rises in serum PSA levels above the nadir obtained at intervals of >2 weeks (Roach et al, 2006; Cookson et al, 2007). Numbers in bold denote significant associations with P-value <0.05.