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. 2006 Feb 28;94(6):820–827. doi: 10.1038/sj.bjc.6603014

Table 2. Demographics in 25 patients with late relapses of MGCT, by mode of detection.

  All Symptoms Routine
n (%) 25 (100) 14 (56) 11 (44)
Agea (years) 30 (20–68) 27 (20–48) 36 (23–68)
       
Primary histology
Seminoma 10 6 4
Non-seminoma 15 8 7
       
UICC stage b
 I 3 2 1
 IS 2 1 1
 II 6 4 2
 III 10 6 4
 Extragonadal 4 1 3
       
IGCCCGc category stage
 Good 11 7 3
 Intermediate 5 2 4
 Poor 3 1 2
       
Chemotherapy in primary treatment
 Seminoma 3 1 2
 Nonseminoma 14 7 7
       
Months to relapsea 55 (32–224) 88 (40–224) 41 (32–110)
       
Sites of relapse
 Retroperitoneal 9 6 3
 Mediastinum 6 3 3
 Lung/pleura 5 2 3
 Neck/supraclavicular 3 1 2
 Retrocrural 1 1  
 Pelvis 3 2 1
       
Number of relapse sites 27d 15d 12d
       
Symptoms leading to unscheduled visit
 Tiredness   4  
 Pain (back/abdominal)   6 (3/3)  
 Dyspnoea   2  
 Peripheral oedema   1  
 Dysphagia   1  
       
Findings at routine follow-up leading to diagnosis
 Radiology (chest X-ray/CT-thorax)     4 (3/1)
 Elevated markers (AFP/HCG)     4 (2/2)
 Palpable masses (supraclv./pelvis)     3 (2/1)
Diameter (mm)a 35 (10–135) 43 (11–135) 20 (10–46)
       
Status
 NEDe 16 10 6
 DODe 7 3 4
 DIDe 2 1 1
a

Median (range).

b

International Union against cancer (Sobin and Wittekind, 2002).

c

International Germ Cell Consensus Classification Group (1997).

d

Three patients experienced the late relapse at two sites, as shown in Tables 2 and 3.

e

Status: NED alive, no evidence of disease; DOD, dead of disease (MGCT); DID, dead of intercurrent disease, tumour-free.