Table 1.
Patient characteristics
| Variable | n (%) |
|---|---|
| Age (years), median (range) | 67.1 (50.6–90.7) |
| Radical radiotherapy | |
| No | 26 (63.4) |
| Yes | 15 (36.6) |
| Prostatectomy | |
| No | 27 (65.9) |
| Yes | 14 (34.1) |
| Histology | |
| CRPC-Adeno | 21 (51.2) |
| CRPC-NE | 20 (48.8) |
| Presence of metastases at diagnosis | |
| No | 19 (46.3) |
| Yes | 22 (53.7) |
| Bone metastases | |
| No | 8 (19.5) |
| Yes | 33 (80.5) |
| Lymph node metastases | |
| No | 18 (43.9) |
| Yes | 23 (56.1) |
| Visceral metastases | |
| No | 19 (46.3) |
| Yes | 22 (56.1) |
| Type of platinum chemotherapy | |
| Combination therapy | 38 (92.7) |
| Monotherapy | 3 (7.3) |
| Number of prior systemic therapies, median (range) |
2 (1–7) |
| Prior AR-directed therapies | |
| No | 18 (43.9) |
| Yes | 23 (56.1) |
| Presence of pain/opiates use at baseline | |
| No | 30 (73.7) |
| Yes | 11 (24.3) |
| Baseline PSA, ng/mL median (range) | 10.5 (0.89–1500) |
| Baseline serum CGA before platinum therapy, ng/mL | |
| CGA < 95 | 19 (46.3) |
| CGA ≥ 95 | 22 (56.1) |
| Baseline serum LDH before platinum therapy, U/L | |
| LDH <192 | 14 (34.1) |
| LDH ≥192 | 27 (65.9) |
| Whole exome data available | |
| No | 9 (22.0) |
| Yes | 32 (78.0) |
| AR alterations | |
| No | 19 (59.4) |
| Yes | 13 (40.6) |
| TP53 alterations | |
| No | 16 (50) |
| Yes | 16 (50) |
| RB1 alterations | |
| No | 17 (53.1) |
| Yes | 15 (46.9) |
| PTEN alterations | |
| No | 17 (53.1 |
| Yes | 15 (46.9) |
| DNA defect repair * alterations | |
| No | 21 (79.7%) |
| Yes | 11 (34.3%) |
DNA repair alterations included BRCA1 and BRCA2 mutation or deletion, and ATM mutation.
Abbreviations. AR, androgen receptor; ATM, ataxia telangiectasia mutated gene; BRCA, breast cancer gene; CGA, chromogranin A; CRPC-Adeno, castration-resistant prostate adenocarcinoma; CRPC-NE, castration-resistant prostate cancer with neuroendocrine features; LDH, lactate dehydrogenase; n, number; PSA, prostate specific antigen; PTEN, phosphatase and tensin homolog; RB1, retinoblastoma 1; TP53, tumor protein p53.