Skip to main content
. 2010 May 25;102(12):1769–1777. doi: 10.1038/sj.bjc.6605684

Table 1. Clinical-pathological data of the patients involved in this study and their association with overall survival.

Parameter No. of patients in TaqMan analysis No. of patients in microarray analysis
Histology    
 ERMS 66 (41%) 31 (37%)
 ARMS 90 (55%) 53 (63%)
  PAX3-FOXO1 fusion gene-positive 45 30
  PAX7-FOXO1 fusion gene-positive 12 8
  Fusion gene-negative 33 15
  RMS not otherwise specified 7 (4%) 0
     
Total 163 84
     
Gender (M/F) 91/72 47/37
     
Median age 5 (0–23) 5.5 (0–21)
     
Primary tumour location    
 Favourable 58 32
 Unfavourable 79 50
 Unknown 26 2
     
SIOP stage    
 Stage I 46 25
 Stage II 44 26
 Stage III 21 9
 Stage IV 43 22
 Unknown 9 2
     
Metastasis    
 Present at diagnosis 43 22
 Absent at diagnosis 108 61
 Unknown 12 1
     
Median survival    
 Median follow-up time 4.0 ya  
     
 Overall survival 9.6 y  
  N of events (N patients) 61 (159)  
     
 Event-free survival 2.8 y  
  N of events (N patient) 79 (159)  

Abbreviations: ARMS=alveolar RMS; ERMS=embryonal RMS; RMS= rhabdomyosarcoma.

a

On the basis of patients with censored data.