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. 2020 Oct 3;21(2):152–164. doi: 10.1038/s41397-020-00191-8

Table 1.

Baseline patient and treatment characteristics and clinical follow-up data (n = 375).

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).