Table 1.
Cases (n = 53) | Controls (n = 322) | p | |||
---|---|---|---|---|---|
Median (range) or n (%) | Missing n (%) | Median (range) or n (%) | Missing n (%) | ||
Age at start chemotherapy (years) | 31 (17–55) | – | 27 (16–55) | – | 0.009 |
Age at follow-up (years) | 51 (24–72) | – | 41 (21–69) | – | <0.001 |
Follow-up duration (years) | 12 (4–37) | – | 11 (3–37) | – | 0.03 |
Royal Marsden Hospital stage | – | 3 (1%) | 0.46 | ||
Stage II | 25 (47%) | 179 (56%) | |||
Stage III | 6 (11%) | 31 (10%) | |||
Stage IV | 22 (42%) | 109 (34%) | |||
IGCCCG classification | 2 (4%) | 3 (1%) | 0.95 | ||
Good | 33 (62%) | 197 (61%) | |||
Intermediate | 14 (26%) | 90 (28%) | |||
Poor | 4 (8%) | 32 (10%) | |||
Chemotherapy regime | – | – | – | ||
BEP followed by EP | 18 (33%) | 129 (40%) | |||
BEP | 17 (32%) | 114 (35%) | |||
PVB followed by PV maintenance | 3 (6%) | 16 (5%) | |||
2 PVB followed by 2 BEP | 1 (2%) | 16 (5%) | |||
PVB | 4 (8%) | 11 (3%) | |||
EP | 5 (9%) | 8 (2%) | |||
CEB | 0 | 10 (3%) | |||
Other platinum-based chemotherapy | 5 (9%) | 18 (6%) | |||
Any radiotherapy | 4 (8%) | – | 4 (1%) | – | – |
Abdominal | 2 (4%) | 2 (0.6%) | |||
Cranial | 0 | 2 (0.6%) | |||
Thoracic | 1 (2%) | 0 | |||
Contralateral testicle | 1 (2%) | 0 | |||
No radiotherapy | 49 (93%) | 318 (99%) | |||
Cardiovascular events | – | – | – | ||
Any event | 53 (100%) | 0 | |||
Cardiomyopathya | 6 (11%) | – | |||
Cerebrovasculara | 8 (15%) | – | |||
Coronarya | 19 (36%) | – | |||
Thromboembolica | 19 (36%) | – | |||
Otherb | 5 (9%) | – | |||
None | 0 | 322 (100%) | |||
Blood pressure at follow-up (mmHg) | 3 (6%) | 26 (8%) | |||
Systolic | 139 (110–190) | 135 (105–190) | 0.07 | ||
Diastolic | 85 (60–112) | 80 (50–124) | 0.07 | ||
BMI at follow-up (kg/m²) | 26.4 (19.4–40.6) | 5 (9%) | 25.5 (19.3–41.7) | 58 (18%) | 0.04 |
Waist-hip ratio at follow-up | 1.0 (0.9–1.3) | 8 (15%) | 1.0 (0.8–1.3) | 95 (30%) | 0.60 |
Metabolic syndrome at follow-up | 5 (9%) | 75 (23%) | <0.001 | ||
Yes | 32 (60%) | 92 (29%) | |||
No | 16 (30%) | 155 (48%) | |||
Antihypertensive drugs at follow-up | – | 4 (1%) | <0.001 | ||
Yes | 27 (51%) | 52 (16%) | |||
No | 26 (49%) | 266 (83%) | |||
Lipid lowering drugs at follow-up | – | 3 (1%) | <0.001 | ||
Yes | 21 (40%) | 27 (8%) | |||
No | 32 (60%) | 292 (91%) | |||
Antidiabetic drugs at follow-up | – | 3 (1%) | 0.06 | ||
Yes | 4 (8%) | 7 (2%) | |||
No | 49 (93%) | 312 (97%) | |||
Testosterone suppletion at follow-up | – | 3 (1%) | 0.75 | ||
Yes | 2 (4%) | 20 (6%) | |||
No | 51 (96%) | 299 (93%) | |||
Fasting glucose at follow-up (mmol/l) | 5.6 (3.5–15.1) | 3 (6%) | 5.4 (1.3–9.4) | 104 (32%) | 0.05 |
Total cholesterol at follow-up (mmol/l) | 4.6 (3.1–7.6) | – | 5.2 (2.8–9.7) | 5 (2%) | <0.001 |
HDL cholesterol at follow-up (mmol/l) | 1.4 (0.8–4.9) | 6 (11%) | 1.2 (0.3–5.6) | 56 (17%) | 0.17 |
LDL cholesterol at follow-up (mmol/l) | 2.9 (1.2–5.8) | 6 (11%) | 3.3 (0.4–6.5) | 57 (17%) | 0.03 |
Triglyceride at follow-up (mmol/l) | 1.4 (0.5–4.7) | – | 1.4 (0.4–118) | 4 (1%) | 0.90 |
Total testosterone at follow-up (nmol/l) | 13 (4.7–33) | 6 (11%) | 15 (0.7–160) | 57 (18%) | 0.01 |
eGFR at follow-up (ml/min/1.73 m²) | 90 (18–127) | – | 92 (18–127) | 4 (1%) | 0.02 |
Albuminuria in 24 h urine at follow-up (mg/24 h) | 6 (0.9–1,152) | 33 (62%) | 8 (0–5,850) | 158 (49%) | – |
Chronic kidney disease stage at follow-up | – | 4 (1%) | 0.01 | ||
Stage 4 | 0 | 1 (0.3%) | |||
Stage 3B | 3 (6%) | 1 (0.3%) | |||
Stage 3A | 2 (4%) | 12 (4%) | |||
Stage 2 | 26 (49%) | 130 (40%) | |||
Stage 1 | 22 (42%) | 174 (54%) |
Characteristics of TC patients with and without cardiovascular event were compared with Fisher’s exact test and Mann–Whitney U test after removal of missing values, with two-sided p < 0.05 considered significant.
BEP bleomycin, etoposide, cisplatin, BMI body-mass index, CEB carboplatin, etoposide, bleomycin, eGFR estimated glomerular filtration rate, EP etoposide, cisplatin, HDL high density lipoprotein, IGCCCG International Germ Cell Cancer Collaborative Group, LDL low-density lipoprotein, PV cisplatin, vinblastine, PVB cisplatin, vinblastine, bleomycin.
aPatients with multiple cardiovascular events were counted in multiple categories.
bIntracerebral hemorrhage (n = 1), cardiac arrhythmia (n = 2), and cardiac valve regurgitation or stenosis (n = 2).